
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.)"
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Reagecon Y4 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y4 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 Crystal Violet Solution (non-aqueous indicator) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Crystal Violet Solution (non-aqueous indicator) is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Forma y color:LiquidReagecon Acetone Buffered Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s Acetone Buffered Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color:LiquidReagecon Potassium Hydroxide Alcoholic Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Hydroxide Alcoholic Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 Silver Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Silver Nitrate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon pH 10.00 Ammonium Chloride Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 10.0 Ammonium Chloride Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color:LiquidReagecon Potassium Hydroxide 0.5M in alcohol (60% v/v) according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 0.5M in alcohol (60% v/v) is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.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 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 Methyl Orange mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Orange mixed Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Forma y color:LiquidReagecon Formaldehyde Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Formaldehyde 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 Perchloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Perchloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.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 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 Concentrate to make Antimony (Sb) 1000ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Antimony (Sb) 1000ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.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 Fatty Acid Methyl Ester (FAME) 8 Compound Mix according to European Pharmacopoeia (EP) Chapter 2.4.22-3 Neat
This Reagecon Fatty Acid Methyl Ester (FAME) 8 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 Myristate: 5% w/w. - Methyl Palmitate: 10% w/w. - Methyl Stearate: 15% w/w. - Methyl Arachidate: 20% w/w. - Methyl Oleate: 20% w/w. - Methyl Eicosenoate: 10% w/w. - Methyl Behenate: 10% w/w. - Methyl Lignocerate: 10% w/w.Forma y color:SolidReagecon Potassium Pyroantimonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Pyroantimonate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 Citrate Buffer 0.05M pH 6.00 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Citrate Buffer 0.05M pH 6.00 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Forma y color:LiquidReagecon Phenolphthalein Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phenolphthalein Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator In volumetric titrations, plus as an indicator of pH change as outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 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 traceableForma 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 R3 Colour Reference Solution according to European Pharmacopoeia (EP)
CAS:Reagecon’s R3 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 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 Acetate Buffer pH 4.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Acetate Buffer pH 4.5 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Forma y color:LiquidReagecon Concentrate to make Arsenic (As) 10ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Arsenic (As) 10ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon Sodium Nitrite 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Nitrite 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 Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.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 Acetic Acid (30%) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Acetic Acid (30%) is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), use in limit tests (4.1.2), a component of buffer solutions (4.1.3), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 7.4 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 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.Forma y color:LiquidReagecon Naphtholbenzein Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Naphtholbenzein 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 Dichromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Potassium Dichromate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 Alcoholic 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid Alcoholic 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Simulated Intestinal Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Simulated Intestinal 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 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 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Forma y color: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.Forma y color:LiquidEPO/Erythropoietin Protein, Human, Recombinant
<p>Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.</p>Forma y color:Lyophilized PowderPeso molecular:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.EPO/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%Forma y color:Lyophilized PowderPeso molecular:45.1 kDa (predicted)Diethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Fórmula:C6H14O3Pureza:≥ 99.900%Forma y color:Colourless liquidPeso molecular:134.18N-Nitroso Paroxetine EP Impurity A (N-Nitroso Paroxetine USP Related Compound B, N-Nitroso Desfluoro Paroxetine)
Fórmula:C19H20N2O4Peso molecular:340.38Folinic Acid-d4 Calcium Salt ((6RS)-Calcium Levofolinate EP Impurity H-d4 Calcium Salt , Leucovorin-d4 Calcium Salt)
Fórmula:C20H17D4N7O7·CaPeso molecular:475.46 40.08Tretinoin-d6 (Retinoic Acid-d6, Isotretinoin EP Impurity A-d6)
Fórmula:C20H22D6O2Peso molecular:306.48Metformin EP Impurity F-13C2-d6 HCl (Dacarbazine EP Impurity D-13C2-d6 HCl, Dimethylamine-13C2-d6 HCl)
CAS:Fórmula:C2HD6N·HClPeso molecular:53.11 36.46Dexamethasone-13C3 (Betamethasone EP Impurity A-13C3, Dexamethasone Acetate EP Impurity A-13C3, Dexamethasone Sodium Phosphate EP Impurity A-13C3)
CAS:Fórmula:C1913C3H29FO5Peso molecular:395.44δ 2-Cefpodoxime Proxetil EP Impurity A (δ 2-Cefpodoxime Acid)
CAS:Fórmula:C15H17N5O6S2Peso molecular:427.45N-Nitroso Mesalazine (Mesalamine) EP Impurity K HCl (N-Nitroso Fentanyl EP Impurity F HCl, N-Nitroso Aniline HCl)
CAS:Fórmula:C8H8N2O5SPeso molecular:244.22Nicotine EP Impurity D-2,4,5,6-d4 (Nicotine USP Related Compound D-2,4,5,6-d4, Myosmine-2,4,5,6-d4)
CAS:Fórmula:C9H6D4N2Peso molecular:150.22Insulin Human, recombinant
CAS:Fórmula:C257H383N65O77S6Pureza:95.0 - 105.0 % (dried basis)Forma y color:White to off-white powderPeso molecular:5807.57Hydrocortisone EP Impurity D-d4 (6-β-Hydroxy Hydrocortisone-d4)
CAS:Fórmula:C21H26D4O6Peso molecular:382.49All-rac-α-Tocopheryl Acetate EP Impurity C-d9 (Vitamin E-d9, DL-α-Tocopherol-d9)
Fórmula:C29H41D9O2Peso molecular:439.77Ethyl 4-hydroxybenzoate, Ph. Eur. grade
CAS:Fórmula:C9H10O3Pureza:99.0 - 101.0 %Forma y color:White powderPeso molecular:166.18DL-α-Tocopherol, Ph. Eur., USP grade
CAS:Fórmula:C29H50O2Pureza:96.0 - 102.0 % (USP)Forma y color:Pale yellow to brown, clear viscous liquidPeso molecular:430.72N-Nitroso Ticagrelor EP Impurity B (N-Nitroso Ticagrelor USP Related Compound B)
Fórmula:C23H27F2N7O5SPeso molecular:551.57N-Desmethyl Tetracycline-d3 (N-Desmethyl Oxytetracycline EP Impurity B-d3)
Fórmula:C21H19D3N2O8Peso molecular:433.43Nevirapine EP Impurity B (Nevirapine USP Related Compound B)
CAS:Fórmula:C12H10N4OPeso molecular:226.24Nevirapine EP Impurity C (Nevirapine USP Related Compound C)
CAS:Fórmula:C15H16N4OPeso molecular:268.32D-(-)-Fructose
CAS:Fórmula:C6H12O6Pureza:92.0 - 102.0 % (dried basis)Forma y color:White, hygroscopic, crystalline powderPeso molecular:180.16Nevirapine EP Impurity A (Nevirapine USP Related Compound A)
CAS:Fórmula:C14H14N4OPeso molecular:254.29Iopromide EP Impurity A (Iopromide USP Related Compound A) (Mixture of Diastereomers)
CAS:Fórmula:C15H20I3N3O6Peso molecular:719.05Chlorothiazide-13C,15N2 (Hydrochlorothiazide EP Impurity A-13C,15N2)
CAS:Fórmula:C613CH6ClN15N2O4S2Peso molecular:298.69N-Nitroso Terbinafine EP Impurity A-13C-d3 (N-(Nitroso Terbinafine USP Related Compound A-13C-d3 (Free Form))
Fórmula:C1113CH9D3N2OPeso molecular:204.25Thioridazine EP Impurity B Besylate (Mesoridazine Besylate)
CAS:Fórmula:C21H26N2OS2·C6H6O3SPeso molecular:544.74Anatabine (Nicotine EP Impurity A, (S)-Nicotine USP Related Compound A)
CAS:Fórmula:C10H12N2Peso molecular:160.22Aripiprazole EP Impurity B (Aripiprazole USP Related Compound C (Free Form))
Fórmula:C10H12Cl2N2Peso molecular:231.12rac-Rosuvastatin EP Impurity D-d6 (rac-Rosuvastatin Lactone-d6)
Fórmula:C22H20D6FN3O5SPeso molecular:469.57Risedronate EP Impurity A Disodium Salt (Risedronate USP Related Compound B Disodium Salt)
CAS:Fórmula:C14H18N2Na2O12P4Peso molecular:576.17N-Nitroso Etodolac EP Impurity H (N-Nitroso 7-Ethyl Trypophopl)
Fórmula:C12H14N2O2Peso molecular:218.26Fosinopril EP Impurity E (Fosinopril USP Related Compound E (Free Form), Phenyl Fosinopril)
Fórmula:C30H40NO7PPeso molecular:557.63(S)-Selegiline EP Impurity D ((S)-Selegiline USP Related Compound D (Free Form), (S)-N-Desmethyl Selegiline)
Fórmula:C12H15NPeso molecular:173.40Chlorcyclizine EP Impurity A-d11 (Cyclizine EP Impurity A-d11, Cyclizine USP Related Compound A-d11)
CAS:Fórmula:C5HD11N2Peso molecular:111.23N-Nitroso Verapamil EP Impurity J-d7 (N-Nitroso N-Desmethyl Verapamil-d7, N-Nitroso Norverapamil-d7)
Fórmula:C26H28D7N3O5Peso molecular:476.62Maprotiline EP Impurity C-d4 HCl (N-Desmethyl Maprotiline-d4 HCl)
CAS:Fórmula:C19H17D4N·HClPeso molecular:267.41 36.46N-Nitroso Cyclophosphamide EP Impurity D (N-nitroso Cyclophosphamide USP Related Compound B)
Fórmula:C7H15ClN3O4PPeso molecular:271.64Atropine EP Impurity D (Mixture of Diastereomers) (6-Hydroxyhyoscyamine)
Fórmula:C17H23NO4Peso molecular:305.38N1,N2-Dinitroso Lacosamide EP Impurity A (N1,N2-Dinitroso (S)-Lacosamide)
Fórmula:C13H16N4O5Peso molecular:308.29




