Soluciones y reactivos de la farmacopea europea (EP) (Ph. Eur.)
Las soluciones y reactivos de la Farmacopea Europea (Ph. Eur.) garantizan que los productos farmacéuticos cumplan con los altos estándares de calidad establecidos por la Unión Europea. Estas soluciones son fundamentales para probar la pureza, potencia y calidad de los medicamentos. En CymitQuimica, ofrecemos una amplia gama de soluciones y reactivos que cumplen con la Ph. Eur., apoyando la investigación farmacéutica y los procesos de control de calidad.
Se han encontrado 9876 productos de "Soluciones y reactivos de la farmacopea europea (EP) (Ph. Eur.)"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Lacosamide EP Impurity B (R-Isomer) (Lacosamide USP Related Compound B (R-Isomer), O-Acetyl Lacosamide)
CAS:Fórmula:C14H18N2O4Forma y color:White To Off-White SolidPeso molecular:278.31Naproxen EP Impurity E (Naproxen USP Related Compound E)
CAS:Fórmula:C15H16O3Forma y color:White To Off-White SolidPeso molecular:244.29Triamcinolone Acetonide EP Impurity C (Triamcinolone Acetonide 21-Aldehyde Hydrate)
CAS:Fórmula:C24H31FO7Forma y color:White To Off-White SolidPeso molecular:450.50Zolmitriptan EP Impurity I
CAS:Fórmula:C17H21N3O4Forma y color:White To Off-White SolidPeso molecular:331.37Mexiletine EP Impurity D HCl
CAS:Fórmula:C11H17NO·HClForma y color:White To Off-White SolidPeso molecular:179.26 36.46Atorvastatin EP Impurity P
CAS:Fórmula:C36H39FN2O5Forma y color:White To Off-White SolidPeso molecular:598.72Phenobarbital Sodium EP Impurity E
CAS:Fórmula:C11H15N3OForma y color:White To Off-White SolidPeso molecular:205.26(S)-Solifenacin EP Impurity E
CAS:Fórmula:C7H13NOForma y color:White To Off-White SolidPeso molecular:127.19Limonene Chlorohydrin (Terpin EP Impurity C Chlorohydrin)
CAS:Fórmula:C10H17ClOForma y color:Pale Yellow LiquidPeso molecular:188.70Norgestimate EP Impurity A-d6 (Norgestimate USP Related Compound A-d6)
CAS:Fórmula:C23H24D6O3Peso molecular:360.53(R)-Limonene ((R)-Terpin EP Impurity C)
CAS:Fórmula:C10H16Forma y color:Colorless LiquidPeso molecular:136.24Chlorcyclizine EP Impurity A (Cyclizine EP Impurity A, Cyclizine USP Related Compound A)
CAS:Fórmula:C5H12N2Peso molecular:100.17Ketorolac EP Impurity E (Ketorolac USP Related Compound A)
CAS:Fórmula:C19H22N2O5Peso molecular:358.39Dipyridamole EP Impurity C (Dipyridamole USP Related Compound C)
CAS:Fórmula:C20H30ClN7O2Forma y color:Pale Yellow SolidPeso molecular:435.96Atorvastatin EP Impurity J (Atorvastatin 3-Deoxyhept-2E-Enoic Acid)
CAS:Fórmula:C33H33FN2O4Forma y color:White To Off-White SolidPeso molecular:540.64Tetracycline EP Impurity A-13C2-d6 (4-Epitetracycline-13C2-d6)
CAS:Fórmula:C2013C2H18D6N2O8Peso molecular:452.46Folic Acid (Folinic Acid EP Impurity C)
CAS:Fórmula:C19H19N7O6Forma y color:Yellow SolidPeso molecular:441.40Sulfadiazine EP Impurity C (Sulfadimidine EP Impurity C, Sulfaguanidine)
CAS:Fórmula:C7H10N4O2SPeso molecular:214.24Pheniramine N-Glucuronide (Dexchlorpheniramine EP Impurity A N-Glucuronide) (Mixture of Diastereomers)
CAS:Fórmula:C22H28N2O6Forma y color:White To Off-White SolidPeso molecular:416.47Ceftazidime EP Impurity A
CAS:Fórmula:C22H22N6O7S2Forma y color:White To Off-White SolidPeso molecular:546.57Pheniramine N-Oxide (Dexchlorpheniramine EP Impurity A N-Oxide)
CAS:Fórmula:C16H20N2OForma y color:Pale Yellow Sticky SolidPeso molecular:256.35Alprostadil (Prostaglandin E1) EP Impurity J
CAS:Fórmula:C23H40O5Forma y color:Colourless LiquidPeso molecular:396.57Felypressin EP Impurity D Tetratrifluoroacetate
Fórmula:C92H130N26O22S4·4C2HF3O2Peso molecular:2080.45 4*114.02Ascomycin (Tacrolimus EP Impurity A)
CAS:Fórmula:C43H69NO12Forma y color:White To Off-White SolidPeso molecular:792.02Sitagliptin Tablets EP Impurity FP-E HCl
CAS:Fórmula:C10H10F3NO2·HClForma y color:White To Off-White SolidPeso molecular:233.19 36.46Sorafenib EP Impurity B
CAS:Fórmula:C14H13N3O3Forma y color:Pale Brown-Red SolidPeso molecular:271.28Sorafenib EP Impurity H (Sorafenib USP Related Compound H)
CAS:Fórmula:C21H16ClF3N4O3Forma y color:White To Off-White SolidPeso molecular:464.83Sorafenib EP Impurity I
CAS:Fórmula:C15H8Cl2F6N2OForma y color:White To Off-White SolidPeso molecular:417.13Lacosamide EP Impurity D HCl (Lacosamide USP Related Compound D HCl)
CAS:Fórmula:C11H16N2O2·HClPeso molecular:208.26 36.46Lomustine EP Impurity C (Lomustine USP Related Compound C)
CAS:Fórmula:C13H24N2OPeso molecular:224.35N-Nitroso Desloratadine EP Impurity B (N-Nitroso Iso Desloratadine)
Fórmula:C19H18ClN3OPeso molecular:339.82Cotinine (Nicotine EP Impurity C, Nicotine USP Related Compound C)
CAS:Fórmula:C10H12N2OForma y color:Colorless LiquidPeso molecular:176.22Azathioprine EP Impurity F-13C-15N2 (Didanosine EP Impurity A-13C-15N2, Didanosine USP Related Compound A-13C-15N2, Hypoxanthine-13C-15N2)
CAS:Fórmula:C413CH4N215N2OPeso molecular:139.09Caffeine-13C3 (Pentoxifylline EP Impurity F-13C3, Theophylline EP Impurity A-13C3, Theophylline-Ethylenediamine EP Impurity A-13C3)
CAS:Fórmula:C513C3H10N4O2Forma y color:White To Off-White SolidPeso molecular:197.166-Mercaptopurine-13C-15N2 (Azathioprine EP Impurity B-13C-15N2)
CAS:Fórmula:C413CH4N215N2SPeso molecular:155.15N1-Nitroso Tryptophan EP Impurity I (Mixture of Diastereomers)
CAS:Fórmula:C13H13N3O3Peso molecular:259.27N-Nitroso Labetalol EP Impurity F (N-Nitroso Labetalol USP Related Compound F (Free Form))
Fórmula:C19H21N3O4Peso molecular:355.39Lacosamide EP Impurity D (R-Isomer) (Lacosamide USP Related Compound D (R-Isomer) (Free Form))
CAS:Fórmula:C11H16N2O2Peso molecular:208.26N-Nitroso Atomoxetine EP Impurity B-d3 (N-Nitroso (S)-Atomoxetine-d3) (Mixture of Isomers)
Fórmula:C17H17D3N2O2Peso molecular:287.38Clodronate Disodium EP Impurity D Pyridinium Salt
CAS:Fórmula:CH5ClO6P2·C5H5NPeso molecular:210.44 79.10N-Nitroso-N-Desethyl Lidocaine Hydrochloride Monohydrate EP Impurity K
Fórmula:C11H15N3O2Peso molecular:221.26Prednisolone (Hydrocortisone EP Impurity A)
CAS:Fórmula:C21H28O5Forma y color:White To Off-White SolidPeso molecular:360.45N2-Nitroso Lacosamide EP Impurity B (R-Isomer) (N2-Nitroso Lacosamide USP Related Compound B (R-Isomer), N2-Nitroso O-Acetyl Lacosamide)
Fórmula:C14H17N3O5Peso molecular:307.31Amlodipine EP Impurity B (Methylaminophthaloyl Amlodipine)
CAS:Fórmula:C29H32ClN3O7Forma y color:White To Off-White SolidPeso molecular:570.04N-Nitroso ent-Pseudoephedrine (N-Nitroso ent-Ephedrine HCl EP Impurity B)
CAS:Fórmula:C10H14N2O2Peso molecular:194.23N-Nitroso Chlorcyclizine EP Impurity A-d4 (N-Nitroso Cyclizine EP Impurity A-d4, N-Nitroso Cyclizine USP Related Compound A-d4)
CAS:Fórmula:C5H7D4N3OPeso molecular:133.19Paclitaxel (Docetaxel EP Impurity F)
CAS:Fórmula:C47H51NO14Forma y color:White To Off-White SolidPeso molecular:853.92Cefpodoxime Proxetil EP Impurity D (Mixture of Diastereomers)
CAS:Fórmula:C21H27N5O9S2Peso molecular:557.59Amoxicillin EP Impurity D Sodium Salt (Mixture of Diastereomers)
CAS:Fórmula:C16H20N3O6S·NaPeso molecular:382.41 22.99Tryptophan EP Impurity A HCl (Tryptophan USP Related Compound A HCl)
CAS:Fórmula:C24H26N4O4·HClPeso molecular:434.50 36.46Dipivefrine EP Impurity C HCl and Dipivefrine EP Impurity D HCl
CAS:Fórmula:C14H21NO4·HClPeso molecular:267.33 36.46Desmopressin EP Impurity G Trifluoroacetate
Fórmula:C48H68N14O12S2·C2HF3O2Peso molecular:1097.28 114.02Leuprorelin (Leuprolide) EP Impurity F Ditrifluoroacetate
CAS:Fórmula:C59H84N16O12·2C2HF3O2Peso molecular:1209.42 2*114.02Reagecon 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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon pH 3.78 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 traceableForma y color: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.Forma y color:LiquidReagecon BY1 Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s BY1 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 spectrophotometerForma y color:LiquidReagecon Phenylhydrazine Hydrochloride Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phenylhydrazine Hydrochloride 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.Forma y color:LiquidReagecon R4 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R4 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 spectrophotometerForma y color: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.Forma y color:LiquidReagecon Picric Acid R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Picric Acid R1 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.Forma y color:LiquidReagecon Potassium Tetraiodomercurate Solution Alkaline Part A according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
For Potassium Tetraiodomercurate Solution Alkaline 1071600 both parts 1071600-A and 1071600-B are required Reagecon Potassium Tetraiodomercurate Solution Alkaline Part A 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.Forma y color:LiquidReagecon B6 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B6 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.Forma y color:LiquidReagecon Ferric Ammonium Sulphate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ferric Ammonium Sulphate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in materials for the manufacture of containers (3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - 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.Forma y color:LiquidReagecon Standard Colour Solution BY (Brownish Yellow) according to European Pharmacopoeia (EP) Chapter 2.2.2
CAS:Reagecon's Standard Colour Solution BY (Brownish 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.Forma y color:LiquidReagecon pH 10.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon’s pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableForma y color: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.Forma y color:LiquidReagecon Ninhydrin Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ninhydrin 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.Forma y color: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 traceableForma y color: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.Forma y color: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 traceableForma y color:LiquidReagecon Ruthenium Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon's Ruthenium Red Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Standard Colour Solution B (Brown) according to European Pharmacopoeia (EP) Chapter 2.2.2
CAS:Reagecon's Standard Colour Solution B (Brown) 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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Ammonium Carbonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonium Carbonate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Sodium Hypochlorite Strong Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Sodium Hypochlorite Strong 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.Forma y color:LiquidReagecon Molybdovanadic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Molybdovanadic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color: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 traceableForma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Sodium Dodecyl Sulphate 0.1% w/v in 0.1M Hydrochloric Acid Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's 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.Forma y color: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.Forma y color:LiquidReagecon Bromothymol Blue R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromothymol Blue R1 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.Forma y color:LiquidReagecon 133 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 usedForma y color: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.Forma y color: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.Forma y color: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 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.Forma y color: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.Forma y color:LiquidReagecon Concentrate to make Calcium (Ca) 100ppm Alcoholic Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Calcium (Ca) 100ppm Alcoholic Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon Bromophenol Blue Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromophenol Blue 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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Zinc Chloride 0.05M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Zinc Chloride 0.05M 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.Forma y color: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.Forma y color:LiquidReagecon Ammonium Cerium Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Ammonium Cerium Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color: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.Forma y color:LiquidReagecon BY5 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY5 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 spectrophotometerForma y color:LiquidReagecon Cerium Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Cerium Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon B8 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B8 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Potassium Dichromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Dichromate 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.Forma y color:LiquidReagecon pH 9.00 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 9.0 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color: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.Forma y color: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 spectrophotometerForma y color:LiquidReagecon Acetate Buffer pH 4.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 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.Forma y color: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.Forma y color:LiquidReagecon pH 6.00 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 6.0 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color:LiquidReagecon 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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Alcohol Aldehyde Free according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Alcohol Aldehyde Free is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in volumetric reagents (4.2.2) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Potassium Phosphate pH 5.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 5.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Perchloric Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Perchloric Acid 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.Forma y color:LiquidReagecon Hydrochloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color: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.Forma y color: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 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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Bromophenol Blue R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromophenol Blue 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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Sodium Carbonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sodium Carbonate 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.Forma y color:LiquidReagecon R2 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R2 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 spectrophotometerForma y color: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.Forma y color: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.Forma y color: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 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.Forma y color: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.Forma y color:LiquidReagecon Potassium Phosphate pH 5.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 5.8 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.Forma y color:LiquidReagecon B7 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B7 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Carbon Dioxide Free Water according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Carbon Dioxide Free Water 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.Forma y color: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.Forma y color:LiquidReagecon Fatty Acid Methyl Ester (FAME) 6 Compound Mix according to European Pharmacopoeia (EP) Chapter 2.4.22-1 Neat
This Reagecon Fatty Acid Methyl Ester (FAME) 6 Compound Mix is presented in Neat form (solid). This presentation confers on the user advantages, that include flexibility in terms of matrix type and concentration of standard prepared, easier storage, safer handling and extended shelf life. The product can be used either as a calibrant or analytical control solution for a variety of gas and liquid chromatography methods that include GC, GC-MS, HPLC and LC-MS. This product can also be used to validate appropriate test methods or qualify an instrument in a regulated industry. The esterification of fatty acids is an important tool for both characterising fats and oils and for determining the total fat content in foods and foodstuffs. It is also an important measurement for the assessing of quality and purity of biofuels. Description | Concentration: - Methyl Laurate: 5% w/w. - Methyl Myristate: 5% w/w. - Methyl Palmitate: 10% w/w. - Methyl Stearate: 20% w/w. - Methyl Arachidate: 40% w/w. - Methyl Oleate: 20% w/w.Forma y color:SolidReagecon 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.Forma y color:LiquidReagecon Potassium Tetraiodomercurate Solution Alkaline Part B according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
For Potassium Tetraiodomercurate Solution Alkaline 1071600 both parts 1071600-A and 1071600-B are required Reagecon Potassium Tetraiodomercurate Solution Alkaline Part B 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.Forma y color: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.Forma y color:LiquidReagecon Iodoplatinate Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Iodoplatinate Reagent 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.Forma y color: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.Forma y color: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.Forma y color:LiquidReagecon Potassium Permanganate 0.02M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Permanganate 0.02M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon pH 9.5 Ammonium Chloride Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 9.5 Ammonium Chloride Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color:Liquid
