
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 9867 produtos de "Soluções e Reagentes da Farmacopeia Europeia (EP, Ph. Eur.)"
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Reagecon Benzethonium Chloride 0.004M according to European Pharmacopoeia (EP)
Reagecon’s Benzethonium Chloride 0.004M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stoichiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon BY7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY7 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerCor 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 B2 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s B2 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Cor e Forma: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.Cor e Forma:LiquidReagecon Acetate Buffer pH 5.8 Dissolution Media in accordance to European Pharmacopoeia (EP)
Reagecon's Acetate Buffer 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.Cor e Forma: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.Cor e Forma:LiquidReagecon Bromocresol Purple 0.04% Indicator Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromocresol Purple 0.04% Indicator Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Cor e Forma: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 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 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.Cor e Forma:LiquidReagecon Concentrate to make Iron (Fe) 20ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Iron (Fe) 20ppm 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 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.Cor e Forma: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.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 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 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 400ml 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 400ml of solution, each 400ml bottle is diluted to give 10L 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 Hydrochloric Acid 1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 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 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 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.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 Diphenylamine Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Diphenylamine Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Cor e Forma:LiquidReagecon R5 Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s R5 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 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 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 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 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.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 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 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.Cor 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 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 6.8 and 0.5% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 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 Simulated Intestinal Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Intestinal Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.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 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 Y1 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon's Y1 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Cor e Forma:LiquidReagecon GY6 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY6 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 B5 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B5 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Cor e Forma: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.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:LiquidDiethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Fórmula:C6H14O3Pureza:≥ 99.900%Cor e Forma:Colourless liquidPeso molecular:134.18EPO/Erythropoietin Protein, Human, Recombinant (hFc)
<p>EPO/Erythropoietin Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag.</p>Pureza:SDS-PAGE: 96.3%; SEC-HPLC: 97.2% - SDS-PAGE: 96.3%; SEC-HPLC: 97.2%Cor e Forma:Lyophilized PowderPeso molecular:45.1 kDa (predicted)EPO/Erythropoietin Protein, Human, Recombinant
<p>Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.</p>Cor e Forma:Lyophilized PowderPeso molecular:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.Chlorcyclizine EP Impurity A-d11 (Cyclizine EP Impurity A-d11, Cyclizine USP Related Compound A-d11)
CAS:Fórmula:C5HD11N2Peso molecular:111.23Cyproheptadine EP Impurity A (Cyproheptadine USP Related Compound A)
CAS:Fórmula:C15H12Peso molecular:192.26Cisatracurium Besilate EP Impurity N Benzenesulfonate
Fórmula:C32H44NO8·C6H5O3SPeso molecular:570.71 157.17Dihydro Ergotamine Mesylate EP Impurity E (9,10-Dihydroergocristine)
CAS:Fórmula:C35H41N5O5Peso molecular:611.75Vancomycin CDP-1 (Vancomycin EP Impurity B and Vancomycin EP Impurity E)
CAS:Fórmula:C66H74Cl2N8O25Peso molecular:1450.25Phenytoin EP Impurity A-d5 (Dimenhydrinate EP Impurity J-d5)
CAS:Fórmula:C13H5D5OPeso molecular:187.25Mesalazine (Mesalamine) EP Impurity G Ethanolamine
CAS:Fórmula:C7H6O4·C2H7NOPeso molecular:154.12 61.08L-Cysteine hydrochloride monohydrate, Ph. Eur., USP grade
CAS:Fórmula:C3H7NO2S·HCl·H2OPureza:≤ 0.5%Cor e Forma:White or almost white crystalline powder, or colourless crystalsPeso molecular:175.64Betamethasone EP Impurity G
CAS:Fórmula:C22H30O5Cor e Forma:White To Off-White SolidPeso molecular:374.48Ref: 4Z-F-1020
5mgA consultar10mgA consultar25mgA consultar50mgA consultar100mgA consultar300mg19.206,00€Potassium iodide, 99%, Ph. Eur., BP, USP grade
CAS:Fórmula:KICor e Forma:White to almost white powder or colourless crystalsPeso molecular:166.01Almotriptan EP Impurity D (Almotriptan USP Related Compound B)
CAS:Fórmula:C15H21N3O2SC4H4O4Peso molecular:307.41 1/2*116.07Cytosine (Gemcitabine EP Impurity A, Lamivudine EP Impurity E, Cytarabine EP Impurity C)
CAS:Fórmula:C4H5N3OPeso molecular:111.10N-Nitroso Salbutamol EP Impurity I (R-isomer) (N-Nitroso Levalbuterol USP Related Compound F)
Fórmula:C20H26N2O4Peso molecular:358.44Cisatracurium Besilate EP Impurity H Besylate
CAS:Fórmula:C53H72N2O12·2C6H5O3SPeso molecular:929.16 2 157.16N-Nitroso Omeprazole EP Impurity C (N-Nitroso Omeprazole USP Related Compound C, N-Nitroso Esomeprazole EP Impurity C)
Fórmula:C17H18N4O3SPeso molecular:358.42Cefpodoxime Proxetil EP Impurity E (Mixture of Diastereomers)
CAS:Fórmula:C22H27N5O10S2Cor e Forma:White To Off-White SolidPeso molecular:585.60Azithromycin EP Impurity B (Azithromycin B)
CAS:Fórmula:C38H72N2O11Cor e Forma:White To Off-White SolidPeso molecular:733.00Rac-Levodopa EP Impurity A (Rac-Levodopa USP Related Compound A, 6-Hydroxy DOPA)
CAS:Fórmula:C9H11NO5Peso molecular:213.19Methotrexate EP Impurity C (Methotrexate USP Related Compound C)
CAS:Fórmula:C20H21N7O6Peso molecular:455.43Galantamine EP Impurity E-13C,d3 (N-Desmethyl Galanthamine-13C,d3)
Fórmula:C1513CH16D3NO3Peso molecular:277.34Liothyronine EP Impurity C-13C6 (Levothyroxine EP Impurity C-13C6)
CAS:Fórmula:C813C6H9I3O4Peso molecular:627.89N-Nitroso Caffeine EP Impurity F (N-Nitroso Caffeine USP Related Compound F, N-Nitroso Paraxanthine)
Fórmula:C7H7N5O3Peso molecular:209.17(Z)-Montelukast EP Impurity I Sodium Salt (Mixture of Diastereomers)
Fórmula:C35H35ClNO4S·NaPeso molecular:601.18 22.99(R,R)-Galantamine EP Impurity A HBr ((+)-Narwedine HBr, (+)-Galanthaminone HBr)
CAS:Fórmula:C17H21NO3·HBrPeso molecular:287.36 80.91Calcium sulfate dihydrate, BP, Ph. Eur. grade
CAS:Fórmula:CaSO4·2H2OPureza:(Titration) 98.0 - 102.0 % (CaSO4 · 2H2O)Cor e Forma:White or almost white fine powderPeso molecular:172.17(+)-trans-Limonene Oxide ((+)-trans-Terpin EP Impurity C Oxide)
CAS:Fórmula:C10H16OPeso molecular:152.24N-Nitroso Selegiline EP Impurity D (N-Nitroso Selegiline USP Related Compound D (Free Form), N-Nitroso-N-Desmethyl Selegiline)
Fórmula:C12H14N2OPeso molecular:202.26N-Nitroso rac-Anatabine-d4 (N-Nitroso rac-Nicotine EP Impurity A-d4, N-Nitroso Nicotine USP Related Compound A-d4)
CAS:Fórmula:C10H7D4N3OPeso molecular:193.24Omeprazole EP Impurity I-13C-d3 (Omeprazole USP Related Compound I-13C-d3, Omeprazole Sulfone N-Oxide-13C-d3) (on pyridine)
Fórmula:C1613CH16D3N3O5SPeso molecular:381.43Ketamine EP Impurity A (Z-isomer) HCl (Ketamine USP Related Compound A (Z-isomer HCl )
CAS:Fórmula:C13H16ClNO·HClPeso molecular:237.73 36.46Omeprazole EP Impurity C-13C-d3 (Omeprazole USP Related Compound C-13C-d3, Esomeprazole EP Impurity C-13C-d3) (on pyridine)
Fórmula:C1613CH16D3N3O2SPeso molecular:333.43Tropisetron EP Impurity A-d3 (Deptropine EP Impurity A-d3, Tropine-d3)
CAS:Fórmula:C8H12D3NOPeso molecular:144.23Hydrocortisone EP Impurity L-d8 ((Hydrocortisone Acetate EP Impurity B-d8, Oxenol-d8)
Fórmula:C21H22D8O4Peso molecular:354.52Potassium bromide, BP, Ph. Eur. grade
CAS:Fórmula:KBrPureza:(Titration) 98.0 - 100.5 % (dried substance)Cor e Forma:Colourless crystals or white crystalline powderPeso molecular:119.01N-Nitroso Verapamil EP Impurity J-d7 (N-Nitroso N-Desmethyl Verapamil-d7, N-Nitroso Norverapamil-d7)
Fórmula:C26H28D7N3O5Peso molecular:476.62Venlafaxine EP Impurity D-13C-d3 HCl (Venlafaxine USP Related Compound A-13C-d3, N-Desmethyl Venlafaxine-13C-d3 HCl)
CAS:Fórmula:C1513CH22D3NO2·HClPeso molecular:267.39 36.46Warfarin EP Impurity C (Benzalacetone) (Mixture of E/Z Isomers)
CAS:Fórmula:C10H10OPeso molecular:146.19Doxepin EP Impurity C-d3 HCl ((E)-Doxepin USP Related Compound C-d3, Desmethyl (E)-Doxepin-d3 HCl, (E)-Nordoxepin-d3 HCl)
Fórmula:C18H16D3NO·HClPeso molecular:268.38 36.466-Mercaptopurine-13C2-15N (Azathioprine EP Impurity B-13C2-15N)
CAS:Fórmula:C213CH4N315NSPeso molecular:155.15Hydrocortisone EP Impurity D-d4 (6-β-Hydroxy Hydrocortisone-d4)
CAS:Fórmula:C21H26D4O6Peso molecular:382.49N1,N2-Dinitroso Lacosamide EP Impurity A (N1,N2-Dinitroso (S)-Lacosamide)
Fórmula:C13H16N4O5Peso molecular:308.29Doxepin EP Impurity C-13C-d3 HCl ((E)-Doxepin USP Related Compound C-13C-d3, Desmethyl (E)-Doxepin-13C-d3 HCl, (E)-Nordoxepin-13C-d3 HCl)
CAS:Fórmula:C1713CH16D3NO·HClPeso molecular:269.37 36.46




