Soluções e Reagentes da Farmacopeia Europeia (EP, Ph. Eur.)
As soluções e reagentes da Farmacopeia Europeia (Ph. Eur.) garantem que os produtos farmacêuticos atendam aos altos padrões de qualidade estabelecidos pela União Europeia. Essas soluções são essenciais para testar a pureza, potência e qualidade dos medicamentos. Na CymitQuimica, oferecemos uma ampla gama de soluções e reagentes em conformidade com a Ph. Eur., apoiando a pesquisa farmacêutica e os processos de controle de qualidade.
Foram encontrados 9875 produtos de "Soluções e Reagentes da Farmacopeia Europeia (EP, Ph. Eur.)"
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Lansoprazole EP Impurity E (Rabeprazole EP Impurity F, Rabeprazole USP Related Compound C, 2-Mercaptobenzimidazole)
CAS:Fórmula:C7H6N2SCor e Forma:White To Off-White SolidPeso molecular:150.20Oxytocin EP Impurity I Trifluoroacetate
CAS:Fórmula:C43H65N11O13S2·C2HF3O2Cor e Forma:White To Off-White SolidPeso molecular:1008.18 114.02Bisacodyl EP Impurity C (Bisacodyl USP Related Compound C)
CAS:Fórmula:C20H17NO3Cor e Forma:White To Off-White SolidPeso molecular:319.36Indomethacin (Indometacin) EP Impurity A (Indomethacin USP Related Compound B, Acemetacin EP Impurity A, Bezafibrate EP Impurity B, Clopamide EP Impurity B)
CAS:Fórmula:C7H5ClO2Peso molecular:156.57Ethinylestradiol EP Impurity I (6,7-Didehydro Ethynyl Estradiol)
CAS:Fórmula:C20H22O2Peso molecular:294.39Cholecalciferol EP Impurity D (Iso-Tachysterol 3)
CAS:Fórmula:C27H44OCor e Forma:Pale Yellow Semi-SolidPeso molecular:384.65Etoposide EP Impurity B (cis-Etoposide)
CAS:Fórmula:C29H32O13Cor e Forma:White To Off-White SolidPeso molecular:588.56Propyl 4-hydroxybenzoate, Ph. Eur. grade
CAS:Fórmula:C10H12O3Pureza:≤ 0.5%Cor e Forma:White crystalline powderPeso molecular:180.20Fluocinolone Acetonide EP Impurity F
CAS:Fórmula:C24H33FO5Cor e Forma:White To Off-White SolidPeso molecular:420.52Tranexamic Acid EP Impurity B
CAS:Fórmula:C8H15NO2Cor e Forma:White To Off-White SolidPeso molecular:157.21Etoposide EP Impurity A
CAS:Fórmula:C37H38O15Cor e Forma:White To Off-White SolidPeso molecular:722.70Ethinylestradiol EP Impurity E (6-α-Hydroxy Ethinylestradiol)
CAS:Fórmula:C20H24O3Peso molecular:312.41Quetiapine EP Impurity B DiHCl (Quetiapine USP Related Compound B)
CAS:Fórmula:C17H17N3S·2HClCor e Forma:White To Off-White SolidPeso molecular:295.40 2*36.46Enalapril EP Impurity H HCl (Mixture of Diastereomers)
Fórmula:C20H34N2O5·HClCor e Forma:White To Off-White SolidPeso molecular:382.50 36.46Ethinylestradiol EP Impurity B (Ethinyl Estradiol USP Related Compound B (Free Form))
CAS:Fórmula:C20H22O2Peso molecular:294.39Ganciclovir EP Impurity A
CAS:Fórmula:C9H10ClN5O2Cor e Forma:White To Off-White SolidPeso molecular:255.66Methotrexate EP Impurity I Sodium Salt (Methotrexate-1-Monomethyl Ester Sodium Salt)
CAS:Fórmula:C21H23N8O5·NaPeso molecular:467.47 22.99Duloxetine EP Impurity C HBr
CAS:Fórmula:C18H19NOS·HBrCor e Forma:Off-White SolidPeso molecular:297.42 80.91Ursodiol USP Related Compound H (Ursodeoxycholic Acid EP Impurity H, Isoursodeoxycholic Acid)
CAS:Fórmula:C24H40O4Peso molecular:392.58Citalopram EP Impurity A HCl (Citalopram USP Related Compound A HCl, Escitalopram EP Impurity A HCl)
CAS:Fórmula:C20H23FN2O2·HClCor e Forma:White To Off-White SolidPeso molecular:342.42 36.46Potassium Clavulanate EP Impurity G Enantiomer
CAS:Fórmula:C13H15NO6Cor e Forma:White To Off-White SolidPeso molecular:281.26Ethinylestradiol EP Impurity F (6-β-Hydroxy Ethinylestradiol)
CAS:Fórmula:C20H24O3Peso molecular:312.41Escitalopram EP Impurity H HCl (Citalopram USP Related Compound E, Citalopram N-Oxide HCl)
CAS:Fórmula:C20H21FN2O2·HClCor e Forma:White To Off-White SolidPeso molecular:340.40 36.46Laureth-9, Ph. Eur., USP grade
CAS:Cor e Forma:White or almost white, waxy mass (20°C); Clear, colourless liquid (40°C)Ropivacaine EP Impurity F
CAS:Fórmula:C17H24N2OCor e Forma:White To Off-White SolidPeso molecular:272.39Fenoterol EP Impurity B HCl
CAS:Fórmula:C17H19NO4·HClCor e Forma:White To Off-White SolidPeso molecular:301.35 36.46Aprepitant EP Impurity C
CAS:Fórmula:C29H25F7N4O3Cor e Forma:White To Off-White SolidPeso molecular:610.53Furosemide EP Impurity D
CAS:Fórmula:C17H17N3O6SCor e Forma:White To Off-White SolidPeso molecular:391.40Anastrozole EP Impurity F Monohydrate (Escitalopram EP Impurity J Monohydrate, Lisinopril EP Impurity B Monohydrate, Sultamicillin EP Impurity B Monohydrate, Tizanidine EP Impurity I Monohydrate)
CAS:Fórmula:C7H8O3S·H2OCor e Forma:White To Off-White SolidPeso molecular:172.20 18.02Lidocaine EP Impurity A HCl (Bupivacaine EP Impurity F HCl, Ropivacaine EP Impurity H HCl, Ropivacaine USP Related Compound A)
CAS:Fórmula:C8H11N·HClPeso molecular:121.18 36.46Carbetapentane citrate salt, BP, Ph. Eur. grade
CAS:Fórmula:C20H31NO3·C6H8O7Pureza:≤ 0.1%Cor e Forma:White or almost white crystalline powderPeso molecular:525.59Iopromide EP Impurity C (Mixture of Diastereomers)
CAS:Fórmula:C17H22I3N3O8Cor e Forma:White To Off-White SolidPeso molecular:777.09N-Nitroso Quetiapine EP Impurity B (N-Nitroso Quetiapine USP Related Compound B)
Fórmula:C17H16N4OSPeso molecular:324.40Dienogest EP Impurity D
CAS:Fórmula:C22H29NO3Cor e Forma:White To Off-White SolidPeso molecular:355.48Clindamycin HCl (Clindamycin Phosphate EP Impurity E HCl)
CAS:Fórmula:C18H33ClN2O5S·HClCor e Forma:White To Off-White SolidPeso molecular:424.99 36.46Omeprazole EP Impurity C-d3 (Omeprazole USP Related Compound C-d3, Esomeprazole EP Impurity C-d3) (on Pyridine)
CAS:Fórmula:C17H16D3N3O2SPeso molecular:332.44Sotalol EP Impurity A
CAS:Fórmula:C12H20N2O2SCor e Forma:White To Off-White SolidPeso molecular:256.36rac-Cotinine-d4 (rac-Nicotine EP Impurity C-d4, rac-Nicotine USP Related Compound C-d4)
CAS:Fórmula:C10H8D4N2OCor e Forma:Colorless LiquidPeso molecular:180.24Bicalutamide EP Impurity A (Desfluoro Bicalutamide)
CAS:Fórmula:C18H15F3N2O4SCor e Forma:White To Off-White SolidPeso molecular:412.38Indomethacin (Indometacin) EP Impurity H-d4 (Indomethacin Methyl Ester-d4)
CAS:Fórmula:C20H14D4ClNO4Cor e Forma:Pale Yellow SolidPeso molecular:375.84Budesonide EP Impurity E (Budesonide USP Related Compound E, 14,15-Dehydro Budesonide)
CAS:Fórmula:C25H32O6Cor e Forma:White To Off-White SolidPeso molecular:428.53Pefloxacin EP Impurity H
CAS:Fórmula:C12H9ClFNO3Cor e Forma:White To Off-White SolidPeso molecular:269.66Triclabendazole EP Impurity A (Triclabendazole S-Oxide)
CAS:Fórmula:C14H9Cl3N2O2SCor e Forma:Off-White SolidPeso molecular:375.65Potassium Clavulanate EP Impurity H
CAS:Fórmula:C4H11NCor e Forma:Colorless LiquidPeso molecular:73.14(R)-Anatabine DiHCl ((R)-Nicotine EP Impurity A DiHCl, (R)-Nicotine USP Related Compound A DiHCl)
CAS:Fórmula:C10H12N2·2HClPeso molecular:160.22 2*36.46Norvancomycin HCl (Vancomycin EP Impurity A HCl)
CAS:Fórmula:C65H73Cl2N9O24·HClPeso molecular:1435.24 36.46Alimemazine EP Impurity A L-Tartrate (Trimeprazine Sulfoxide L-Tartrate)
CAS:Fórmula:C18H22N2OS·C4H6O6Cor e Forma:White To Off-White SolidPeso molecular:314.45 150.09Titanium dioxide, 99%, Ph. Eur., BP, USP grade
CAS:Fórmula:TiO2Pureza:98.0 - 100.5 % (EP)Cor e Forma:White to almost white powderPeso molecular:79.87Haloperidol Decanoate EP Impurity A HCl
Fórmula:C31H42FNO3·HClCor e Forma:White To Off-White SolidPeso molecular:495.68 36.46Isosorbide Dinitrate EP Impurity C (Isosorbide 5-Mononitrate) (Diluted with Lactose)
CAS:Fórmula:C6H9NO6Cor e Forma:White To Off-White SolidPeso molecular:191.14Fingolimod EP Impurity G HCl (Mono-O-Acetyl Fingolimod HCl)
CAS:Fórmula:C21H35NO3·HClCor e Forma:Off-White Semi-SolidPeso molecular:349.52 36.46Fingolimod EP Impurity E HCl
CAS:Fórmula:C35H57NO2·HClCor e Forma:White To Off-White SolidPeso molecular:523.85 36.46Amoxicillin EP Impurity E (Mixture of Diastereomers)
CAS:Fórmula:C15H21N3O4SCor e Forma:White To Off-White SolidPeso molecular:339.41Bisoprolol EP Impurity K (Bisoprolol USP Related Compound F)
CAS:Fórmula:C18H29NO5Cor e Forma:White To Off-White SolidPeso molecular:339.43Lacosamide EP Impurity G
CAS:Fórmula:C9H11NOCor e Forma:White To Off-White SolidPeso molecular:149.19Spironolactone EP Impurity I
Fórmula:C24H36O4SCor e Forma:White To Off-White SolidPeso molecular:420.61Propylene glycol, Ultrapure, 99.5%, BP, Ph. Eur., USP grade
CAS:Fórmula:C3H8O2Pureza:≥ 99.5%Cor e Forma:Clear, colourless, viscous liquidPeso molecular:76.10Fluvoxamine EP Impurity E Maleate
CAS:Fórmula:C15H22F2N2O2·C4H4O4Cor e Forma:White To Off-White SolidPeso molecular:300.35 116.07Carprofen EP Impurity C
CAS:Fórmula:C14H12ClNOCor e Forma:White To Off-White SolidPeso molecular:245.71Methotrexate EP Impurity K (Folinic Acid EP Impurity A)
CAS:Fórmula:C12H14N2O5Cor e Forma:Light Brown SolidPeso molecular:266.25rac-Cotinine-d3 (rac-Nicotine EP Impurity C-d3, rac-Nicotine USP Related Compound C-d3)
CAS:Fórmula:C10H9D3N2OPeso molecular:179.24rac-Cotinine-d7 (rac-Nicotine EP Impurity C-d7, rac-Nicotine USP Related Compound C-d7)
CAS:Fórmula:C10H5D7N2OPeso molecular:183.26Amisulpride EP Impurity H HCl
CAS:Fórmula:C18H29N3O4S·HClCor e Forma:Pale Yellow SolidPeso molecular:383.51 36.46Orbifloxacin EP Impurity D HCl
CAS:Fórmula:C19H21F2N3O4·HClCor e Forma:Off-White SolidPeso molecular:393.39 36.46Fluocinonide (Fluocinolone Acetonide EP Impurity M)
CAS:Fórmula:C26H32F2O7Cor e Forma:White To Off-White SolidPeso molecular:494.53Fenticonazole EP Impurity C Nitrate
CAS:Fórmula:C24H20Cl2N2O3S·HNO3Cor e Forma:White To Off-White SolidPeso molecular:487.40 63.01Prednisolone (Hydrocortisone EP Impurity A)
CAS:Fórmula:C21H28O5Cor e Forma:White To Off-White SolidPeso molecular:360.45Permethrin EP Impurity C (3-Phenoxybenzyl Alcohol)
CAS:Fórmula:C13H12O2Cor e Forma:Colorless LiquidPeso molecular:200.24Metoprolol EP Impurity A (Metoprolol USP Related Compound A)
CAS:Fórmula:C14H23NO3Cor e Forma:White To Off-White SolidPeso molecular:253.34Etonogestrel EP Impurity D (Etonogestrel USP Related Compound A)
CAS:Fórmula:C20H26O2Peso molecular:298.43Atorvastatin EP Impurity H (Atorvastatin USP Related Compound H, Atorvastatin Lactone)
CAS:Fórmula:C33H33FN2O4Cor e Forma:White To Off-White SolidPeso molecular:540.64Betamethasone-d5 (Betamethasone Acetate EP Impurity A-d5, Betamethasone Dipropionate EP Impurity A-d5, Betamethasone Valerate EP Impurity A-d5, Dexamethasone EP Impurity B-d5)
CAS:Fórmula:C22H24D5FO5Cor e Forma:White To Off-White SolidPeso molecular:397.50Atenolol EP Impurity A (Atenolol USP Related Compound A
CAS:Fórmula:C8H9NO2Cor e Forma:White To Off-White SolidPeso molecular:151.17Desmopressin EP Impurity D Trifluoroacetate (8-L-Arginine Trifluoroacetate)
CAS:Fórmula:C46H64N14O12S2·C2HF3O2Peso molecular:1069.24 114.02All-rac-alfa-Tocopherol EP Impurity A (Mixture of Diastereomers)
CAS:Fórmula:C29H50O2Cor e Forma:Pale Brown LiquidPeso molecular:430.72Leuprorelin (Leuprolide) EP Impurity B
CAS:Fórmula:C59H84N16O12Cor e Forma:White To Off-White SolidPeso molecular:1209.42Reagecon Concentrate to make Sulphate (SO₄) 10ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Sulphate (SO?) 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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Iodine Bromide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Iodine Bromide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in Iodine value (2.5.4) 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.Cor e Forma:LiquidReagecon Sodium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Hydroxide 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Sodium Hydroxide Solution Dilute according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sodium Hydroxide Solution Dilute according to European Pharmacopoeia Chapter 4 (4.1.1) 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.Cor e Forma: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.Cor e Forma:LiquidReagecon GY3 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY3 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 spectrophotometerCor e Forma: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 traceableCor e Forma:LiquidReagecon pH 4.60 Acetate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 4.6 Acetate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableCor e Forma:LiquidReagecon Concentrate to make Aluminium (Al) 100ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Aluminium (Al) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Cor e Forma:LiquidReagecon BY2 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY2 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 spectrophotometerCor e Forma:LiquidReagecon B3 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B3 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Cor e Forma:LiquidReagecon Ninhydrin R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ninhydrin R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Holmium Perchlorate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Holmium Perchlorate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in control of wavelenght for spectrophotmoters (2.2.25). - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Potassium Phosphate pH 7.4 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 7.4 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.Cor e Forma: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 traceableCor e Forma: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.Cor e Forma:LiquidReagecon Sodium Hydroxide 1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Hydroxide 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 ± 0.1%. 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.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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 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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Potassium Phosphate pH 7.4 Dissolution Media in accordance to Chinese (CP) United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.4 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Cor e Forma:LiquidReagecon Ammonium Cerium Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Ammonium Cerium 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.Cor e Forma: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 spectrophotometerCor e Forma:LiquidReagecon Ammonia Dilute R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonia Dilute R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), a component of buffer solutions (4.1.3) and used as a reagent in the performance of tests outlined in several EP monographs. - 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.Cor e Forma:LiquidReagecon Potassium Phosphate pH 7.4 Dissolution Media in accordance to Chinese (CP) United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.4 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Cor e Forma:LiquidReagecon Potassium Phosphate pH 7.2 Dissolution Media in accordance to 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.Cor e Forma: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 traceableCor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Sodium Thiosulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Thiosulphate 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.Cor e Forma:LiquidReagecon pH 5.5 Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 5.5 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 traceableCor e Forma:LiquidReagecon pH 7.40 Phosphate Buffer Saline Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 7.4 Phosphate Buffer Saline 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 traceableCor e Forma: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.Cor e Forma:LiquidReagecon pH 7.41 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableCor e Forma:LiquidReagecon GY5 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY5 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 spectrophotometerCor e Forma: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.Cor e Forma:LiquidReagecon Starch Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Starch 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.Cor e Forma: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.Cor e Forma:LiquidReagecon Potassium Phosphate pH 6.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.Cor e Forma:LiquidReagecon HCL Dilution Matrix (10g/L HCl) according to European Pharmacopoeia (EP)
Reagecon’s HCl Dilution Matrix (10g/L HCl) 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.Cor e Forma: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.Cor e Forma:LiquidReagecon Lead Acetate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Lead Acetate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Hydrochloric Acid Dilute R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Hydrochloric Acid Dilute R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - 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.Cor e Forma:LiquidReagecon Hydrochloric Acid 0.01N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.01N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Thioacetamide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Thioacetamide 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.Cor e Forma:LiquidReagecon Concentrate to make Calcium (Ca) 10ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Calcium (Ca) 10ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Cor e Forma: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 traceableCor e Forma:LiquidReagecon Silver Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Silver Nitrate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Hydrochloric Acid 3M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 3M 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.Cor e Forma:LiquidReagecon Crystal Violet Solution (non-aqueous indicator) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Crystal Violet Solution (non-aqueous 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.Cor e Forma: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.Cor e Forma:LiquidReagecon Copper Sulphate 0.02M according to European Pharmacopoeia (EP)
Reagecon's Copper Sulphate 0.02M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon AVL 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.Cor e Forma: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 spectrophotometerCor e Forma:LiquidReagecon Hydrochloric Acid 2M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 2M 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.Cor e Forma: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.Cor e Forma:LiquidReagecon R1 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R1 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 spectrophotometerCor e Forma:LiquidReagecon B4 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B4 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Cor e Forma: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.Cor e Forma:LiquidReagecon Potassium Hydroxide Alcoholic 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 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.Cor e Forma:LiquidReagecon GY7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY7 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerCor e Forma: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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Hydrochloric Acid R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Produto ControladoReagecon Hydrochloric Acid R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in heavy metals (2.4.8), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon Fuchsin Solution Decolorised R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Fuchsin Solution Decolorised R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma: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 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.Cor e Forma: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.Cor e Forma:LiquidReagecon GY1 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY1 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 spectrophotometerCor e Forma: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.Cor e Forma: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 usedCor e Forma: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.Cor e Forma:LiquidReagecon Lead Acetate Cotton according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Lead Acetate Cotton is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications.Reagecon 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.Cor e Forma:LiquidReagecon Anisaldehyde Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Anisaldehyde 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.Cor e Forma: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.Cor e Forma: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.Cor e Forma:LiquidReagecon Concentrate to make Cadmium (Cd) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Cadmium (Cd) 0.1% Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Cor e Forma:LiquidReagecon Nile Blue A Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Nile Blue A Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Cor e Forma: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.Cor e Forma:LiquidReagecon Acetate Buffer pH 5.5 Dissolution Media in accordance to European Pharmacopoeia (EP)
Reagecon's Acetate Buffer pH 5.5 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.Cor e Forma: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 traceableCor e Forma: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.Cor e Forma:LiquidReagecon Methyl Orange mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Orange mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Cor e Forma: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.Cor e Forma:LiquidReagecon Ammonia Dilute R2 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonia Dilute R2 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma: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.Cor e Forma: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 spectrophotometerCor e Forma:LiquidReagecon Phosphate Buffer Solution R1 pH 6.80 according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 6.8 R1 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 traceableCor e Forma: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.Cor e Forma:LiquidReagecon Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Cor e Forma:LiquidReagecon Methoxyphenylacetic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Methoxyphenylacetic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible.Cor e Forma: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 spectrophotometerCor e Forma: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.Cor e Forma:LiquidReagecon Hydrochloric Acid 0.1N and 0.5% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N and 0.5% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Cor e Forma:Liquid
