European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents
European Pharmacopoeia (EP) solutions and reagents ensure that pharmaceutical products meet the high-quality standards set by the European Union. These solutions are critical in testing the purity, potency, and quality of drugs. CymitQuimica offers a comprehensive range of Ph. Eur.-compliant solutions and reagents, supporting pharmaceutical research and quality control processes.
Found 9858 products of "European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents"
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Acetylsalicylic Acid EP Impurity A-13C6 (Salicylic Acid EP Impurity A-13C6, Salicylic Acid USP Related Compound A-13C6)
CAS:Formula:C13C6H6O3Color and Shape:White To Off-White SolidMolecular weight:144.08Paracetamol EP Impurity N
CAS:Formula:C16H16N2O3Color and Shape:Off-White SolidMolecular weight:284.32Hydroxychloroquine Sulfate EP Impurity D-d5 (Chloroquine USP Related Compound D-d5, Desethyl Chloroquine-d5)
CAS:Formula:C16H17D5ClN3Color and Shape:White To Off-White SolidMolecular weight:296.85Dextrorphan Hemitartrate (Dextromethorphan EP Impurity B Hemitartrate)
CAS:Formula:C17H23NO·C4H6O6Color and Shape:Off-White SolidMolecular weight:2*257.38 150.09Atenolol EP Impurity D (Atenolol USP Related Compound D)
CAS:Formula:C11H14ClNO3Color and Shape:White To Off-White SolidMolecular weight:243.69Glycerol Monocaprylocaprate, Ph. Eur., USP-NF grade
Color and Shape:Colourless or slightly yellow oily liquid or semi-solidNifedipine EP Impurity B (Dehydronitroso Nifedipine)
CAS:Formula:C17H16N2O5Color and Shape:Pale Blue SolidMolecular weight:328.32Liothyronine EP Impurity E (Levothyroxine EP Impurity E)
CAS:Formula:C15H13I2NO4Color and Shape:Pale Brown SolidMolecular weight:525.08Polyethylene glycol 400, BP, Ph. Eur., USP/NF grade
CAS:Formula:CH2CH2OnColor and Shape:Clear, viscous, colourless or almost colourless hygroscopic liquidMolecular weight:~400Potassium nitrate, EP, USP grade
CAS:Formula:KNO3Purity:99.0 - 101.0 %Color and Shape:White to almost white crystalline powder or granulesMolecular weight:101.11Terazosin EP Impurity A (Alfuzosin EP Impurity B, Prazosin EP Impurity A)
CAS:Formula:C10H10ClN3O2Color and Shape:White To Off-White SolidMolecular weight:239.66Terlipressin EP Impurity J Ditrifluoroacetate
Formula:C54H77N15O16S2·2C2HF3O2Molecular weight:1256.42 2*114.02Clodronate Disodium EP Impurity A Pyridinium Salt
CAS:Formula:C4H10Cl2O6P2·C5H5NMolecular weight:286.97 79.10Glipizide EP Impurity J
CAS:Formula:C17H20N4O5SColor and Shape:White To Off-White SolidMolecular weight:392.43Desogestrel EP Impurity E (3-β-Hydroxy Desogestrel)
CAS:Formula:C22H30O2Color and Shape:White To Off-White SolidMolecular weight:326.48Azithromycin EP Impurity J
CAS:Formula:C30H58N2O9Color and Shape:White To Off-White SolidMolecular weight:590.80Salmeterol EP Impurity C
CAS:Formula:C24H35NO4Color and Shape:White To Off-White SolidMolecular weight:401.55Methylprednisolone Acetate EP Impurity A (20R Isomer)
CAS:Formula:C24H34O6Color and Shape:White To Off-White SolidMolecular weight:418.53Trimetazidine EP Impurity F DiHCl
CAS:Formula:C14H22N2O3·2HClColor and Shape:White To Off-White SolidMolecular weight:266.34 2*36.46Homatropine Methylbromide EP Impurity A Bromide
Formula:C17H22NO3·BrColor and Shape:White To Off-White SolidMolecular weight:288.37 79.90Terlipressin EP Impurity B Ditrifluoroacetate (Des-1,2-Diglycine-Terlipressin Ditrifluoroacetate)
CAS:Formula:C48H68N14O13S2·2C2HF3O2Molecular weight:1113.28 2*114.02Fenofibrate EP Impurity B-d6 (Fenofibrate USP Related Compound B-d6, Fenofibric Acid-d6)
CAS:Formula:C17H9D6ClO4Color and Shape:White To Off-White SolidMolecular weight:324.79Repaglinide EP Impurity B (Repaglinide Related Compound B)
CAS:Formula:C13H16O5Color and Shape:White To Off-White SolidMolecular weight:252.27Vancomycin EP Impurity C Trifluoroacetate (Aglucovancomycin B Trifluoroacetate)
CAS:Formula:C53H52Cl2N8O17·C2HF3O2Molecular weight:1143.95 114.02Cefamandole EP Impurity E
CAS:Formula:C19H18N2O8SColor and Shape:White To Off-White SolidMolecular weight:434.42Phloroglucinol EP Impurity O (4,6-Dichlororesorcinol)
CAS:Formula:C6H4Cl2O2Color and Shape:Off-White SolidMolecular weight:179.00Azelastine EP Impurity C
CAS:Formula:C15H11ClO3Color and Shape:White To Off-White SolidMolecular weight:274.70Phenylephrine EP Impurity D (Phenylephrine USP Related Compound D)
CAS:Formula:C16H19NO2Color and Shape:White To Off-White SolidMolecular weight:257.33Ciprofloxacin EP Impurity F HCl
CAS:Formula:C17H19N3O4·HClColor and Shape:Pale Yellow SolidMolecular weight:329.36 36.46Escitalopram EP Impurity K Oxalate ((R)-Citalopram Oxalate)
CAS:Formula:C20H21FN2O·C2H2O4Color and Shape:White To Off-White SolidMolecular weight:324.40 90.03Goserelin EP Impurity K Ditrifluoroacetate
CAS:Formula:C61H86N18O15·2C2HF3O2Molecular weight:1311.47 2*114.02Levothyroxine EP Impurity K (3,3',5'-Triiodo-L-Thyronine)
CAS:Formula:C15H12I3NO4Color and Shape:White To Off-White SolidMolecular weight:650.98Pyridoxine EP Impurity A HCl
CAS:Formula:C8H9NO2·HClColor and Shape:Pale Yellow SolidMolecular weight:151.17 36.46Oxcarbazepine EP Impurity M (Oxcarbazepine USP Related Compound D)
CAS:Formula:C30H22N4O3Color and Shape:Pale Yellow SolidMolecular weight:486.53Cytarabine EP Impurity I
CAS:Formula:C10H15N3O5Color and Shape:White To Off-White SolidMolecular weight:257.25Raltegravir EP Impurity B
Formula:C19H24FN5O3Color and Shape:White To Off-White SolidMolecular weight:389.43Valproic Acid EP Impurity J
CAS:Formula:C11H21NColor and Shape:Pale Yellow LiquidMolecular weight:167.30Tramadol EP Impurity E HCl (Tramadol USP Related Compound B)
CAS:Formula:C9H17NO·HClColor and Shape:White To Off-White SolidMolecular weight:155.24 36.46Aripiprazole EP Impurity G (Aripiprazole Dimer Impurity)
CAS:Formula:C48H56Cl4N6O4Color and Shape:White To Off-White SolidMolecular weight:922.81Lovastatin EP Impurity B Sodium Salt (Lovastatin Hydroxy Acid Sodium Salt)
CAS:Formula:C24H37O6·NaColor and Shape:White To Off-White SolidMolecular weight:421.55 22.99Trimethoprim EP Impurity G
CAS:Formula:C15H20N4O3Color and Shape:White To Off-White SolidMolecular weight:340.35Naphazoline EP Impurity A (Naphazoline USP Related Compound A)
CAS:Formula:C14H16N2OColor and Shape:White To Off-White SolidMolecular weight:228.30Amorolfine EP Impurity E HCl (trans-Amorolfine HCl) (Mixture of Diastereomers)
CAS:Formula:C21H35NO·HClColor and Shape:White To Off-White SolidMolecular weight:317.52 36.46N-Nitroso Zolmitriptan EP Impurity G (N-Nitroso Zolmitriptan USP Related Compound A, N-Nitroso-N-Desmethyl Zolmitriptan)
CAS:Formula:C15H18N4O3Color and Shape:Off-White SolidMolecular weight:302.33Deferasirox EP Impurity E
CAS:Formula:C23H19N3O4Color and Shape:White To Off-White SolidMolecular weight:401.43rac-Aspartame EP Impurity C (DL-Phenylalanine)
CAS:Formula:C9H11NO2Color and Shape:White To Off-White SolidMolecular weight:165.19Cilastatin EP Impurity H
Formula:C15H26N2O3SColor and Shape:White To Off-White SolidMolecular weight:314.44Modafinil EP Impurity C
CAS:Formula:C16H16O3SColor and Shape:White To Off-White SolidMolecular weight:288.36Etoposide EP Impurity R
CAS:Formula:C50H50O20Color and Shape:White To Off-White SolidMolecular weight:970.93Goserelin EP Impurity J Ditrifluoroacetate
Formula:C64H91N19O15·2C2HF3O2Molecular weight:1366.55 2*114.02Cefamandole EP Impurity A
CAS:Formula:C17H16N2O6SColor and Shape:White To Off-White SolidMolecular weight:376.38Levodopa EP Impurity C (Levodopa USP Related Compound B, DL-3-O-Methyldopa)
CAS:Formula:C10H13NO4Color and Shape:White To Off-White SolidMolecular weight:211.22Benzyl benzoate, BP, Ph. Eur. grade
CAS:Formula:C14H12O2Purity:(GC) 99.0 - 100.5 %Color and Shape:Clear, colourless or almost colourless liquid (20°C)Molecular weight:212.25Digoxin EP Impurity I
CAS:Formula:C43H66O15Color and Shape:White To Off-White SolidMolecular weight:822.99Clenbuterol EP Impurity B HCl
CAS:Formula:C12H16Cl2N2O·HClColor and Shape:White To Off-White SolidMolecular weight:275.18 36.46Ivermectin EP Impurity C (Avermectin B2a)
CAS:Formula:C48H74O15Color and Shape:White To Off-White SolidMolecular weight:891.11Lercanidipine EP Impurity B
CAS:Formula:C18H20N2O6Color and Shape:Yellow SolidMolecular weight:360.37Hydroxychloroquine Sulfate EP Impurity D DiHCl (Chloroquine USP Related Compound D DiHCl, Desethyl Chloroquine DiHCl)
CAS:Formula:C16H22ClN3·2HClColor and Shape:White To Off-White SolidMolecular weight:291.83 2*36.46Trimethoprim EP Impurity I (E-Isomer)
CAS:Formula:C19H20N2O3Color and Shape:Off-White SolidMolecular weight:324.38Fluphenazine Decanoate EP Impurity D DiHCl
CAS:Formula:C30H40F3N3O2S·2HClColor and Shape:White To Off-White SolidMolecular weight:563.72 2*36.46Citalopram EP Impurity F HCl (Citalopram USP Related Compound H HCl)
CAS:Formula:C19H21BrFNO·HClColor and Shape:White To Off-White SolidMolecular weight:378.29 36.46Mefenamic Acid EP Impurity E
CAS:Formula:C14H15NColor and Shape:Pale Yellow SolidMolecular weight:197.28Leuprorelin (Leuprolide) EP Impurity C
CAS:Formula:C59H84N16O12Color and Shape:White To Off-White SolidMolecular weight:1209.42Beclometasone (Beclomethasone) Dipropionate EP Impurity Q
Formula:C28H38O6Color and Shape:White To Off-White SolidMolecular weight:470.61Ursodeoxycholic Acid EP Impurity F
CAS:Formula:C24H38O4Color and Shape:White To Off-White SolidMolecular weight:390.56Omeprazole EP Impurity C (Omeprazole USP Related Compound C, Esomeprazole EP Impurity C)
CAS:Formula:C17H19N3O2SColor and Shape:White To Off-White SolidMolecular weight:329.42Ciprofloxacin EP Impurity A
CAS:Formula:C13H9ClFNO3Color and Shape:White To Off-White SolidMolecular weight:281.67Lercanidipine EP Impurity E HCl
CAS:Formula:C20H27NO·HClColor and Shape:White To Off-White SolidMolecular weight:297.44 36.46Warfarin EP Impurity B (4-Hydroxy Coumarin)
CAS:Formula:C9H6O3Color and Shape:White To Off-White SolidMolecular weight:162.14Dequalinium EP Impurity B Iodide
Formula:C30H39N4·IColor and Shape:Pink SolidMolecular weight:455.67 126.91Almotriptan EP Impurity F Malate
CAS:Formula:C19H29N3O2S·C4H6O5Color and Shape:Off-White SolidMolecular weight:363.53 134.09Tetracycline EP Impurity D (Chlortetracycline EP Impurity I, Lymecycline EP Impurity D, 4-Epianhydrotetracycline)
CAS:Formula:C22H22N2O7Molecular weight:426.43Ticlopidine EP Impurity J DiHCl
CAS:Formula:C16H18Cl2N2·2HClColor and Shape:White To Off-White SolidMolecular weight:309.23 2*36.46Formoterol EP Impurity C (Mixture of Diastereomers)
CAS:Formula:C20H26N2O4Color and Shape:Off-White SolidMolecular weight:358.44Diazepam EP Impurity B
CAS:Formula:C16H13Cl2NO2Color and Shape:Pale Yellow SolidMolecular weight:322.19Haloperidol Decanoate EP Impurity J HCl
CAS:Formula:C32H43ClFNO3·HClColor and Shape:White To Off-White SolidMolecular weight:544.16 36.46Reagecon GY7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY7 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon Sulphuric Acid Dilute Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sulphuric Acid Dilute Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Sodium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Hydroxide 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Nitrate (NO₃) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Nitrate (NO?) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Zinc Chloride Formic Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Zinc Chloride Formic Acid Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1). - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Hydrochloric Acid Dilute according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Hydrochloric Acid Dilute is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in heavy metals (2.4.8), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Diphenylamine Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Diphenylamine Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Lead Acetate Paper according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Lead Acetate Paper is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications.Reagecon Acetate Buffer pH 4.5 and 0.5% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 and 0.5% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Hydrochloric Acid 0.01N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.01N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Potassium Iodobismuthate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodobismuthate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Barium Chloride R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Barium Chloride R1 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Phosphate (PO₄) 5ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Phosphate (PO?) 5ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Perchloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Perchloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon pH 7.40 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 7.4 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon Mercuric Nitrate 0.02M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Mercuric Nitrate 0.02M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Y2 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon's Y2 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon pH 9.00 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 9.0 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon Hydrochloric Acid 0.1N and 0.5% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N and 0.5% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Alcohol Aldehyde Free according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Alcohol Aldehyde Free is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in volumetric reagents (4.2.2) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Phosphate pH 7.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 7.5 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Ammonium Carbonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonium Carbonate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Y3 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y3 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon B3 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B3 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Dimidium Bromide - Sulphan Blue Mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Dimidium Bromide - Sulphan Blue Mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Standard Colour Solution Y (Yellow) according to European Pharmacopoeia (EP) Chapter 2.2.2
CAS:Reagecon's Standard Colour Solution Y (Yellow) is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Standard Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Concentrate to make Zinc (Zn) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Zinc (Zn) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Potassium Phosphate pH 5.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 5.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 230.85ml in volume in each bottle and the contents of each bottle can be diluted to produce 6L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 230.85ml of solution, each 230.85ml bottle is diluted to give 6L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Benzethonium Chloride 0.004M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Benzethonium Chloride 0.004M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Phenol Red R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Phenol Red R2 Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Simulated Intestinal Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Intestinal Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Ammonium (NH4) 2.5 ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Ammonium (NH4) 2.5 ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Concentrate to make Chloride (Cl) 8ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Chloride (Cl) 8ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon pH 4.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Lead (Pb) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Lead (Pb) 0.1% Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Fuchsin Solution Decolorised R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Fuchsin Solution Decolorised R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Tetramethylammonium Hydroxide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Tetramethylammonium Hydroxide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in materials for the manufacture of containers (3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Antimony (Sb) 1000ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Antimony (Sb) 1000ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Holmium Perchlorate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Holmium Perchlorate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in control of wavelenght for spectrophotmoters (2.2.25). - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Molybdovanadic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Molybdovanadic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Methoxyphenylacetic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Methoxyphenylacetic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible.Color and Shape:LiquidReagecon Concentrate to make Aluminium (Al) 100ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Aluminium (Al) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Phosphate pH 6.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.1N Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Ammonia Dilute R2 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonia Dilute R2 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Nickel (Ni) 10ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Nickel (Ni) 10ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Concentrate to make Calcium (Ca) 400ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Calcium (Ca) 400ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Potassium Phosphate pH 7.4 Dissolution Media in accordance to Chinese (CP) United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.4 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon B7 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B7 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon pH 4.60 Acetate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 4.6 Acetate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon Fuchsin Solution Decolorised according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Fuchsin Solution Decolorised is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), a component of buffer solutions (4.1.3) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon B8 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B8 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon pH 10.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Nile Blue A Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Nile Blue A Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Silver Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Silver Nitrate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Ruthenium Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon's Ruthenium Red Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon pH 6.87 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon pH 9.5 Ammonium Chloride Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 9.5 Ammonium Chloride Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon Acetate Buffer pH 4.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Acetate Buffer pH 4.5 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Cupri-Citric Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Cupri-Citric Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Methyl Orange mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Orange mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Potassium Hydroxide 1.0M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 1.0M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Sulphate (SO₄) 10ppm R1 Standard according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Sulphate (SO₄) 10ppm R1 Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Dimidium Bromide - Sulphan Blue Mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Dimidium Bromide - Sulphan Blue Mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Concentrate to make Iron (Fe) 8ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Iron (Fe) 8ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Acetic Acid Dilute (12%) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Acetic Acid Dilute (12%) is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in limit tests (4.1.2), a component of buffer solutions (4.1.3), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Hydroxide 0.5M in alcohol (60% v/v) according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 0.5M in alcohol (60% v/v) is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Iodide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Y1 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon's Y1 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Concentrate to make Cadmium (Cd) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Cadmium (Cd) 0.1% Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Magnesium Chloride 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Magnesium Chloride 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon pH 7.41 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Bromocresol Green, Methyl Red mixed Indicator according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromocresol Green, Methyl Red mixed Indicator is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon pH 3.50 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 3.6 Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon BY4 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY4 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon Potassium Hydroxide 0.5M in Alcohol (10% v/v) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Hydroxide 0.5M in Alcohol (10% v/v) is a high purity stable product developed and tested for several European Pharmacopoeia (EP) applications. These include the preparation of other reagents as specified in section (4.1.1). - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Hydrochloric Acid/Sodium Chloride pH 1.2 Dissolution Media in accordance to European Pharmacopoeia (EP)
Reagecon's Hydrochloric Acid/Sodium Chloride pH 1.2 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1N and 1.0% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N and 1.0% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Potassium Hydroxide Alcoholic Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Hydroxide Alcoholic Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Ammonium Thiocyanate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Ammonium Thiocyanate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Dimidium Bromide - Sulphan Blue Mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Dimidium Bromide - Sulphan Blue Mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Sodium Hydroxide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sodium Hydroxide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include a component of buffer solutions (4.1.3) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon GY1 to GY7 Colour Reference Set according to European Pharmacopoeia (EP)
Reagecon’s GY1 to GY7 Colour Reference Set is formulated as a set of reference solutions for the examination of the degree of colour of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. These products are produced by combining Reagecon Primary Colour Solutions - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon Congo Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Congo Red Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Potassium Iodide and Starch Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide and Starch Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator as outlined in individual EP product monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Chloride (Cl) 5ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Chloride (Cl) 5ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Ferric Ammonium Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Ferric Ammonium Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Iodine 0.01M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Iodine 0.01M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon R1 to R7 Colour Reference Set according to European Pharmacopoeia (EP)
Reagecon’s R1 to R7 Colour Reference Set is formulated as a set of reference solutions for the examination of the degree of colour of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. These products are produced by combining Reagecon Primary Colour Solutions - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon Zinc Acetate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Zinc Acetate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Calcium (Ca) 10ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Calcium (Ca) 10ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon pH 3.50 Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 3.5 Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColor and Shape:LiquidReagecon B4 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B4 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Potassium Iodobismuthate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodobismuthate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Potassium Phosphate pH 7.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.5 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Sulfomolybdic R3 Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sulfomolybdic R3 Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. Used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Iodide Saturated Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide Saturated Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the determination of peroide value (2.5.5) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Methyl Red mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Red mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Methyl Orange Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Orange Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon B2 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s B2 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Concentrate to make Calcium (Ca) 100ppm Alcoholic Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Calcium (Ca) 100ppm Alcoholic Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Standard Colour Solution GY (Greenish Yellow) according to European Pharmacopoeia (EP) Chapter 2.2.2
Reagecon's Standard Colour Solution GY (Greenish Yellow) is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Standard Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Cerium Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Cerium Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.1N Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:Liquid
