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 9864 products of "European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents"
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Moxonidine EP Impurity C (4-Hydroxymoxonidine)
CAS:Formula:C9H13N5O2Color and Shape:White To Off-White SolidMolecular weight:223.24Ritonavir EP Impurity O
CAS:Formula:C37H48N6O5S2Color and Shape:White To Off-White SolidMolecular weight:720.95Budesonide EP Impurity D (Mixture of Diastereomers)
CAS:Formula:C25H32O6C25H34O7Color and Shape:Yellow SolidMolecular weight:428.53 446.54Fenoterol EP Impurity A (S, R-Isomer)
CAS:Formula:C17H21NO4Color and Shape:Off-White SolidMolecular weight:303.36Chloramphenicol EP Impurity A
CAS:Formula:C9H12N2O4Color and Shape:Off-White SolidMolecular weight:212.21Etodolac EP Impurity C (Etodolac USP Related Compound A)
CAS:Formula:C16H19NO3Color and Shape:Off-White SolidMolecular weight:273.33Desmopressin EP Impurity G
Formula:C48H68N14O12S2Color and Shape:White To Off-White SolidMolecular weight:1097.28Tryptophan EP Impurity J
CAS:Formula:C22H23N3O4Color and Shape:White To Off-White SolidMolecular weight:393.45Leflunomide EP Impurity H (Teriflunomide EP Impurity B, Teriflunomide USP Related Compound B)
CAS:Formula:C10H7F3N2OColor and Shape:Off-White SolidMolecular weight:228.17Fluticasone Propionate EP Impurity D (Fluticasone Propionate USP Related Compound D)
CAS:Formula:C25H32F2O5SColor and Shape:White To Off-White SolidMolecular weight:482.58Prasugrel EP Impurity A
CAS:Formula:C20H21NO3SColor and Shape:White To Off-White SolidMolecular weight:355.45Pindolol EP Impurity F
CAS:Formula:C11H12ClNO2Color and Shape:White To Off-White SolidMolecular weight:225.67Ticagrelor EP Impurity E (R)-Mandelate
CAS:Formula:C9H9F2N·C8H8O3Color and Shape:White To Off-White SolidMolecular weight:169.17 152.15Mesalazine (Mesalamine) EP Impurity G
CAS:Formula:C7H6O4Color and Shape:Off-White SolidMolecular weight:154.12Itraconazole EP Impurity D
CAS:Formula:C34H36Cl2N8O4Color and Shape:Off-White SolidMolecular weight:691.61Theophylline EP Impurity C (Theophylline USP Related Compound C, Theophylline-Ethylenediamine EP Impurity C, Caffeine EP Impurity B)
CAS:Formula:C7H10N4O3Color and Shape:White To Off-White SolidMolecular weight:198.18Flumazenil EP Impurity A
CAS:Formula:C13H10FN3O3Color and Shape:White To Off-White SolidMolecular weight:275.24Betamethasone Acetate EP Impurity D (Betamethasone Acetate USP Related Compound D)
CAS:Formula:C24H30O6Color and Shape:White To Off-White SolidMolecular weight:414.50D-a-Tocopherol succinate, EP grade
CAS:Formula:C33H54O5Purity:96.0 - 102.0 %Color and Shape:White to yellow powderMolecular weight:530.78Enalaprilat EP Impurity C
Formula:C18H24N2O5Color and Shape:White To Off-White SolidMolecular weight:348.40Hyoscine hydrobromide, BP, Ph. Eur. grade
CAS:Formula:C17H21NO4·HBr·3H2OPurity:≤ 0.1%Color and Shape:White or almost white crystalline powder, or colourless crystalsMolecular weight:438.31Articaine EP Impurity J
CAS:Formula:C10H12BrNO3SColor and Shape:White To Off-White SolidMolecular weight:306.17Bisoprolol EP Impurity T
CAS:Formula:C14H17NO4Color and Shape:White To Off-White SolidMolecular weight:263.29Griseofulvin, EP grade
CAS:Formula:C17H17ClO6Purity:≤ 0.75%Color and Shape:White or pale yellow powderMolecular weight:352.77Penicillin G sodium salt, Ph. Eur. grade
CAS:Formula:C16H17N2NaO4SColor and Shape:White or almost white crystalline powderMolecular weight:356.37Potassium Clavulanate EP Impurity E Dipotassium Salt
CAS:Formula:C16H16N2O10·2KMolecular weight:396.31 2*39.10Hydrocortisone EP Impurity D 21-Butyrate (6-β-Hydroxy Hydrocortisone 21-Butyrate)
Formula:C25H36O7Molecular weight:448.56Ketoprofen, EP grade
CAS:Formula:C16H14O3Purity:(Titration) 99.0 - 100.5 % (dried basis)Color and Shape:White to almost white crystalline powderMolecular weight:254.29Methyldopa EP Impurity C
CAS:Formula:C12H17NO4Color and Shape:White To Off-White SolidMolecular weight:239.27Rosuvastatin EP Impurity C (5-Oxo Rosuvastatin)
CAS:Formula:C22H26FN3O6SColor and Shape:Yellow SolidMolecular weight:479.52Pregabalin EP Impurity A ((S)-Pregabalin USP Related Compound C, (S)-Pregabalin Lactam Impurity)
CAS:Formula:C8H15NOColor and Shape:Colorless LiquidMolecular weight:141.21Sitagliptin Phosphate Monohydrate EP Impurity C
CAS:Formula:C16H16F5N5OColor and Shape:White To Off-White SolidMolecular weight:389.33Gabapentin EP Impurity A (Gabapentin USP Related Compound A)
CAS:Formula:C9H15NOColor and Shape:White To Off-White SolidMolecular weight:153.23Losartan EP Impurity L
CAS:Formula:C44H44Cl2N12OColor and Shape:White To Off-White SolidMolecular weight:827.82Chloramphenicol EP Impurity B
CAS:Formula:C7H5NO3Color and Shape:White To Off-White SolidMolecular weight:151.12Rivaroxaban EP Impurity E
CAS:Formula:C19H19N3O5SColor and Shape:Pale Yellow SolidMolecular weight:401.44Octreotide EP Impurity I Trifluoroacetate
CAS:Formula:C51H68N10O11S2·C2HF3O2Molecular weight:1061.30 114.02Docetaxel EP Impurity E (10-Deacetyl Baccatin III)
CAS:Formula:C29H36O10Color and Shape:White To Off-White SolidMolecular weight:544.60Bromocriptine EP Impurity F
CAS:Formula:C32H40BrN5O5Color and Shape:Brown SolidMolecular weight:654.61Goserelin EP Impurity I Tritrifluoroacetate
Formula:C69H98N20O16·3C2HF3O2Molecular weight:1463.67 3*114.02Rivastigmine EP Impurity C (Rivastigmine USP Related Compound D)
CAS:Formula:C12H15NO3Color and Shape:Off-White Solid (Low M P )Molecular weight:221.26Buserelin EP Impurity C Ditrifluoroacetate
CAS:Formula:C49H74N12O10·2C2HF3O2Color and Shape:White To Off-White SolidMolecular weight:991.21 2*114.02Amoxicillin EP Impurity I
CAS:Formula:C8H9NO3Color and Shape:White To Off-White SolidMolecular weight:167.16Tinidazole EP Impurity A (Tinidazole USP Related Compound A)
CAS:Formula:C4H5N3O2Color and Shape:Off-White SolidMolecular weight:127.10Terazosin EP Impurity J
CAS:Formula:C19H27N5O4Color and Shape:White To Off-White SolidMolecular weight:389.46Raltegravir EP Impurity C
CAS:Formula:C20H23FN6O6Color and Shape:White To Off-White SolidMolecular weight:462.44Dutasteride EP Impurity D (Dutasteride 17-alfa-5-ene)
CAS:Formula:C27H28F6N2O2Molecular weight:526.52Bicalutamide EP Impurity C (Deshydroxy Bicalutamide)
CAS:Formula:C18H14F4N2O3SColor and Shape:White To Off-White SolidMolecular weight:414.37Bisoprolol EP Impurity E (Dehydroxy Bisoprolol) (Mixture of Z and E Isomers)
CAS:Formula:C18H29NO3Color and Shape:Pale Yellow Brown OilMolecular weight:307.43Celiprolol EP Impurity B
CAS:Formula:C31H46N4O7Color and Shape:White To Off-White SolidMolecular weight:586.73Dexamethasone Sodium Phosphate EP Impurity H
CAS:Formula:C22H32FO8PColor and Shape:White To Off-White SolidMolecular weight:474.46Fluconazole EP Impurity H
CAS:Formula:C11H10BrF2N3OColor and Shape:White To Off-White SolidMolecular weight:318.12Fexofenadine EP Impurity C
CAS:Formula:C31H39NO2Color and Shape:White To Off-White SolidMolecular weight:457.66Epinastine EP Impurity B HBr (7-Bromo Epinastine HBr)
CAS:Formula:C16H14BrN3·HBrColor and Shape:White To Off-White SolidMolecular weight:328.21 80.91Minocycline EP Impurity B (Sancycline)
CAS:Formula:C21H22N2O7Color and Shape:Off-White SolidMolecular weight:414.41Hyoscine Butylbromide EP Impurity B (Hyoscine EP Impurity C, Ipratropium Bromide EP Impurity C, Atropine EP Impurity C, Hyoscyamine EP Impurity A, Tropicamide EP Impurity C, Ipratropium Bromide USP Re
CAS:Formula:C9H10O3Color and Shape:White To Off-White SolidMolecular weight:166.18Solifenacin EP Impurity D
Formula:C31H28N2OColor and Shape:White To Off-White SolidMolecular weight:444.58Propranolol EP Impurity B HCl (Mixture of Diastereomers)
CAS:Formula:C29H33NO4·HClColor and Shape:White To Off-White SolidMolecular weight:459.59 36.46Prednisolone EP Impurity I (17-Deoxy Prednisolone)
CAS:Formula:C21H28O4Color and Shape:White To Off-White SolidMolecular weight:344.45Sulfasalazine EP Impurity E Trisodium Salt
CAS:Formula:C29H19N6O7S2·3NaMolecular weight:627.63 3*22.99Benserazide EP Impurity B HCl
CAS:Formula:C17H21N3O8·HClColor and Shape:White To Off-White SolidMolecular weight:395.37 36.46Roxithromycin EP Impurity D
CAS:Formula:C41H76N2O15Color and Shape:White To Off-White SolidMolecular weight:837.06Phenylephrine EP Impurity A HCl (S-Isomer)
CAS:Formula:C8H11NO2·HClColor and Shape:Off-White SolidMolecular weight:153.18 36.46Acetazolamide EP Impurity B
CAS:Formula:C4H5N3OSColor and Shape:White To Off-White SolidMolecular weight:143.16Escitalopram EP Impurity M
CAS:Formula:C20H22FNO3Color and Shape:White To Off-White SolidMolecular weight:343.40Bicalutamide EP Impurity E
Formula:C18H14F4N2O3SColor and Shape:White To Off-White SolidMolecular weight:414.37rac-Carbidopa EP Impurity F (rac-Carbidopa Ethyl Ester)
CAS:Formula:C12H18N2O4Molecular weight:254.29Terpin EP Impurity A (α-Terpineol)
CAS:Formula:C10H18OColor and Shape:Semi-SolidMolecular weight:154.25Gemcitabine EP Impurity B-13C-15N2 HCl (α-Gemcitabine-13C-15N2 HCl)
CAS:Formula:C813CH11F2N15N2O4·HClColor and Shape:White To Off-White SolidMolecular weight:266.18 36.46Methionine EP Impurity B (L-Methionine Sulfone)
CAS:Formula:C5H11NO4SColor and Shape:White To Off-White SolidMolecular weight:181.21Risperidone EP Impurity C (9-Hydroxy Risperidone, Paliperidone)
CAS:Formula:C23H27FN4O3Color and Shape:White To Off-White SolidMolecular weight:426.49Lorazepam EP Impurity E (Lorazepam USP Related Compound C)
CAS:Formula:C15H8Cl2N2OMolecular weight:303.14Loperamide EP Impurity D
CAS:Formula:C29H34N2O2Color and Shape:White To Off-White SolidMolecular weight:442.60Pefloxacin EP Impurity D (Pefloxacin N-Oxide)
CAS:Formula:C17H20FN3O4Color and Shape:Off-White SolidMolecular weight:349.36Cefazolin EP Impurity A
CAS:Formula:C11H12N4O3S3Color and Shape:White To Off-White SolidMolecular weight:344.44Calcipotriol EP Impurity C (Calcipotriene USP Related Compound C, (5E)-Calcipotriene)
CAS:Formula:C27H40O3Color and Shape:White To Off-White SolidMolecular weight:412.61Dorzolamide EP Impurity C HCl
Formula:C10H17BN2O6S3·HClColor and Shape:White To Off-White SolidMolecular weight:368.24 36.46Reagecon Calcium Sulphate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Calcium Sulphate 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/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 BY7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY7 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 Bromocresol Purple 0.04% Indicator Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromocresol Purple 0.04% Indicator 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 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 pH 9.18 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 Potassium Dichromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Potassium Dichromate 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 Hydrochloric Acid 0.01N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.01N 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 R6 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R6 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 Hydrochloric Acid 6M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 6M 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 Lead (Pb) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Lead (Pb) 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 Mordant Black 11 Triturate according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Mordant Black 11 Triturate 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 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 6M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 6M 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 Zinc Chloride Solution Iodinated according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Zinc Chloride Solution Iodinated 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 Concentrate to make Potassium (K) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Potassium (K) 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 Acetone Buffered Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s Acetone Buffered 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 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 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 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 Potassium Phosphate pH 6.0 Dissolution Media in accordance to United States (USP and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.0 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 Potassium Hydroxide Alcoholic 0.5M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide Alcoholic 0.5M 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 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 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 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 pH 9.18 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 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 0.1N 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 Sodium Arsenite 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Arsenite 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. - 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 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 Ammonium Molybdate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonium Molybdate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in determination of Hydroxly value (2.5.3) 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 Cupri-Tartaric Solution 2 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
For Cupri-tartaric Solution 1023300 both parts 1023300-A and 1023300-B are required Reagecon's Cupri-Tartaric Solution 2 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 Citrate Buffer 0.05M pH 6.00 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Citrate Buffer 0.05M pH 6.00 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 Tetrabutylammonium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Tetrabutylammonium 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 Hydrochloric Acid 6M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 6M 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 Bismuth Nitrate 0.01M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Bismuth Nitrate 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 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 B5 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B5 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 Aluminium (Al) 200ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Aluminium (Al) 200ppm 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 1.68 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 Alcoholic 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid Alcoholic 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 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 Zinc Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Zinc 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 Potassium Phosphate pH 6.8 R Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 6.8 R 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 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 Cupri-Tartaric Solution 1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:For Cupri-tartaric Solution 1023300 both parts 1023300-A and 1023300-B are required Reagecon's Cupri-Tartaric Solution 1 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 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 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 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 Potassium Chloride 0.05M Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Chloride 0.05M 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 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 Y6 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y6 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 Sodium Hydroxide Strong Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sodium Hydroxide Strong 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), 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 Ferroin according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ferroin is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator for manual titrations as 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 Y5 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y5 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 Congo Red Paper according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Congo Red Paper 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 1330 µs/cm Conductivity and Resistivity at 20°C according to European Pharmacopoeia (EP)
Reagecon's Conductivity Standard at 20°C is tested and NIST traceable. The product is aqueous based, non-hazardous and accurate to a specification of ± 1%. The product because it is aqueous based, has a low temperature coefficient of variation and guaranteed stability throughout its entire shelf life, even after opening the bottle. This product is formulated, specified and manufactured in compliance with EP requirements. - NIST traceable - This conductivity standard is aqueous based, thereby eliminating any errors attributable to matrix mismatch. Each bottle is supplied with a comprehensive Certificate of Analysis and has a table of conductivity variation with temperature printed on the product label. The low temperature coefficient of variation, reduces measurement errors and enables non-temperature controlled use - High accuracy ± 1% at 20°C, enables the standards to be used as calibrators and/or controls, in accordance with the most exacting requirements - Guaranteed stability throughout entire shelf life, even after opening the bottle, eliminates the need to open a fresh bottle of standard every time it is usedColor and Shape:LiquidReagecon Silver Nitrate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Silver Nitrate R2 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 Potassium Phosphate pH 7.2 Dissolution Media in accordance to Chinese (CP) United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.2 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 B9 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B9 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 10.00 Ammonium Chloride Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 10.0 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 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 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 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 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 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 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 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 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 R7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R7 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 0.5M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sulphuric Acid 0.5M 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 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 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 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 GY2 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY2 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 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 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 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 Ammonium Cerium Nitrate 0.01M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
CAS:Controlled ProductReagecon's Ammonium Cerium Nitrate 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 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 Phenolphthalein Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phenolphthalein Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator In volumetric titrations, plus as an indicator of pH change as 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 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 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 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 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 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 Potassium Chloride 0.1M Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Chloride 0.1M 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 as a component of buffer solutions (4.1.3). - 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 Lead Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Lead 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 B1 to B9 Colour Reference Set according to European Pharmacopoeia (EP)
Reagecon’s B1 to B9 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 B1 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s B1 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 Lanthanum Nitrate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Lanthanum Nitrate 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 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 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 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 Phosphate Buffer pH 4.5 Dissolution Media in accordance to European Pharmacopoeia (EP)
Reagecon's Phosphate 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 Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Simulated Gastric Fluid without Enzyme 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 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 Acetate Buffer pH 4.5 and 1.0% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 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 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 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 Diphenylamine R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Diphenylamine 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) 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 Permanganate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Controlled ProductReagecon Potassium Permanganate 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 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 Sodium Edetate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Edetate 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 Nitric Acid Dilute according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Nitric 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 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 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 Methyl Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Red Indicator 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 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 Hydrogen Phthalate 0.2M according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Hydrogen Phthalate 0.2M is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include as a component of buffer solutions (4.1.3). - 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 Sodium Hydroxide 0.1M Ethanolic according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Hydroxide 0.1M Ethanolic 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 Copper (Cu) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Copper (Cu) 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 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 Benzethonium Chloride 0.004M according to European Pharmacopoeia (EP)
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 stoichiometry, 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:Liquid
