
European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents
European Pharmacopoeia (EP) solutions and reagents ensure that pharmaceutical products meet the high-quality standards set by the European Union. These solutions are critical in testing the purity, potency, and quality of drugs. CymitQuimica offers a comprehensive range of Ph. Eur.-compliant solutions and reagents, supporting pharmaceutical research and quality control processes.
Found 9875 products of "European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents"
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Reagecon Lead Acetate Paper according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Lead Acetate Paper is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications.Reagecon 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.Color and Shape: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.Color and Shape:LiquidReagecon Potassium Hydroxide Alcoholic 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide Alcoholic 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape: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.Color and Shape:LiquidReagecon Zinc Chloride Solution Iodinated according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Zinc Chloride Solution Iodinated is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Ammonium (NH4) 2.5 ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Ammonium (NH4) 2.5 ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon Potassium Dichromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Potassium Dichromate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon 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.Color and Shape:SolidReagecon 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.Color and Shape: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.Color and Shape:LiquidReagecon Potassium Hydroxide Alcoholic 0.5M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide Alcoholic 0.5M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix Method A Reference Solution in n-Heptane according to European Pharmacopoeia (EP) Chapter 2.4.22, Table 3
CAS:This Reagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix is a ready to use product that is 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 identity of each standard is verified using a high performance calibrated Gas Chromatograph Mass Spectrometer (GC-MS Instrument). The mass spectrum of each of the analytes is confirmed by comparison with the National Institute of Standards and Technology (NIST) mass spectral library. - 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: 10% w/w. - Methyl Palmitate: 15% w/w. - Methyl Stearate: 20% w/w. - Methyl Arachidate: 20% w/w. - Methyl Oleate: 10% w/w. - Methyl Eicosenoate: 5% w/w. - Methyl Behenate: 10% w/w. - Methyl Linocerate: 10% w/w.Color and Shape:LiquidReagecon Concentrate to make Calcium (Ca) 10ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Calcium (Ca) 10ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape: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.Color and Shape:LiquidReagecon Silver Nitrate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Silver Nitrate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Silver Nitrate 0.001M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Silver Nitrate 0.001M 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 a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Phosphate pH 6.8 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.Color and Shape:LiquidReagecon pH 6.87 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Benzethonium Chloride 0.004M according to European Pharmacopoeia (EP)
Reagecon’s Benzethonium Chloride 0.004M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stoichiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Phosphomolybdotungstic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phosphomolybdotungstic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Phosphate pH 7.2 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 7.2 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Potassium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Hydrochloric Acid 0.01N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.01N Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon Lead Nitrate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Lead Nitrate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Methyl Orange Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Orange Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape:LiquidReagecon Potassium Iodide Saturated Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide Saturated Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the determination of peroide value (2.5.5) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon 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.Color and Shape:LiquidReagecon Phosphotungstic Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phosphotungstic 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. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Lead Acetate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Lead Acetate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon R7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R7 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon Y7 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y7 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Color and Shape:LiquidReagecon Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Buffered Sodium Dodecyl Sulphate pH 7 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon 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.Color and Shape: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 spectrophotometerColor and Shape:LiquidReagecon Potassium Iodide and Starch Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide and Starch Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator as outlined in individual EP product monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Phosphate pH 6.8 R Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 6.8 R Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon BY4 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY4 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerColor and Shape:LiquidReagecon 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.Color and Shape:LiquidEPO/Erythropoietin Protein, Human, Recombinant (hFc)
<p>EPO/Erythropoietin Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag.</p>Purity:SDS-PAGE: 96.3%; SEC-HPLC: 97.2% - SDS-PAGE: 96.3%; SEC-HPLC: 97.2%Color and Shape:Lyophilized PowderMolecular weight:45.1 kDa (predicted)EPO/Erythropoietin Protein, Human, Recombinant
<p>Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.</p>Color and Shape:Lyophilized PowderMolecular weight:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.Diethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Formula:C6H14O3Purity:≥ 99.900%Color and Shape:Colourless liquidMolecular weight:134.18Sevoflurane EP Impurity A (Sevoflurane USP Related Compound A)
CAS:Formula:C4H2F6OMolecular weight:180.05N-Nitroso Caffeine EP Impurity F (N-Nitroso Caffeine USP Related Compound F, N-Nitroso Paraxanthine)
Formula:C7H7N5O3Molecular weight:209.17Calcium sulfate dihydrate, BP, Ph. Eur. grade
CAS:Formula:CaSO4·2H2OPurity:(Titration) 98.0 - 102.0 % (CaSO4 · 2H2O)Color and Shape:White or almost white fine powderMolecular weight:172.17N-Nitroso rac-Anatabine-d4 (N-Nitroso rac-Nicotine EP Impurity A-d4, N-Nitroso Nicotine USP Related Compound A-d4)
CAS:Formula:C10H7D4N3OMolecular weight:193.24Warfarin EP Impurity C (Benzalacetone) (Mixture of E/Z Isomers)
CAS:Formula:C10H10OMolecular weight:146.19Rabeprazole EP Impurity A-d3 (Rabeprazole USP Related Compound D-d3, Rabeprazole Sulfone-d3)
CAS:Formula:C18H18D3N3O4SMolecular weight:378.46Rac-Levodopa EP Impurity A HCl (Rac-Levodopa USP Related Compound A HCl, 6-Hydroxy DOPA HCl)
CAS:Formula:C9H11NO5·HClColor and Shape:Dark Brown SolidMolecular weight:213.19 36.46Dihydroergocornine (Dihydroergocristine Mesilate EP Impurity F)
CAS:Formula:C31H41N5O5Molecular weight:563.70N1-Nitroso Lacosamide EP Impurity F (S-Isomer) (N1-Nitroso Lacosamide USP Related Compound F (S-Isomer))
Formula:C12H15N3O4Molecular weight:265.27Simvastatin EP Impurity A (Simvastatin Acid, Tenivastatin)
CAS:Formula:C25H40O6Molecular weight:436.59rac-Irinotecan EP Impurity E (rac-Irinotecan USP Related Compound B, rac-7-Ethyl-10-Hydroxy Camptothecin)
Formula:C22H20N2O5Molecular weight:392.42Pantoprazole EP Impurity B-d6 (Pantoprazole USP Related Compound B-d6, Pantoprazole Sulfide-d6)
CAS:Formula:C16H9D6F2N3O3SMolecular weight:373.41N1-Nitroso Benzylpenicillin (Benzathine) EP Impurity C (N1-Nitroso Benzylpenicilloic Acids Benzathine)
Formula:C32H37N5O5SMolecular weight:603.74Metoprolol EP Impurity O-d7 HCl (Metoprolol USP Related Compound D-d7) (Mixture of Diastereomers)
CAS:Formula:C27H34D7NO6·HClMolecular weight:482.67 36.46Solifenacin EP Impurity I-d5 (Solifenacin-N-Oxide-d5)
CAS:Formula:C23H21D5N2O3Molecular weight:383.50N-Nitroso Isoprenaline HCl EP Impurity A (N-Nitroso Isoproterenol USP Related Compound A)
Formula:C11H14N2O4Molecular weight:238.24Phenytoin EP Impurity A-d5 (Dimenhydrinate EP Impurity J-d5)
CAS:Formula:C13H5D5OMolecular weight:187.25Clozapine EP Impurity C HCl Salt
CAS:Formula:C17H17ClN4·HClColor and Shape:Yellow SolidMolecular weight:312.80 36.46ent-Acetylcysteine EP Impurity C (ent-Acetylcysteine USP Related Compound C)
CAS:Formula:C10H16N2O6S2Molecular weight:324.37Methotrexate EP Impurity B (Methotrexate USP Related Compound B)
CAS:Formula:C19H20N8O5Molecular weight:440.42Rotigotine EP Impurity G (Rotigotine USP Related Compound G (Free Form))
CAS:Formula:C22H25NOS2Molecular weight:383.57C5-Nitroso Cytosine (C5-Nitroso Gemcitabine EP Impurity A, C5-Nitroso Lamivudine EP Impurity E, C5-Nitroso Cytarabine EP Impurity C)
Formula:C4H4N4O2Molecular weight:140.10(S)-(-)-Limonene-13C-d2 ((S)-(-)-Terpin EP Impurity C-13C-d2)
CAS:Formula:CC9H14D2Molecular weight:139.246-Mercaptopurine-13C2-15N (Azathioprine EP Impurity B-13C2-15N)
CAS:Formula:C213CH4N315NSMolecular weight:155.15Di-N-Nitroso Cyclophosphamide EP Impurity E (Di-N-Nitroso Cyclophosphamide USP Related Compound D)
Formula:C7H16ClN4O6PMolecular weight:318.65C5-Nitroso Uridine (C5-Nitroso Adenosine EP Impurity F, C5-Nitroso Cytarabine EP Impurity B)
CAS:Formula:C9H11N3O7Molecular weight:273.20N1-Nitroso Cyclophosphamide EP Impurity E (N1-Nitroso Cyclophosphamide USP Related Compound D)
Formula:C7H17ClN3O5PMolecular weight:289.65Methotrexate EP Impurity E-13C-d3 (Methotrexate USP Related Compound E-13C-d3)
Formula:C1413CH12D3N7O2Molecular weight:329.34Tetracycline EP Impurity D HCl (Chlortetracycline EP Impurity I HCl , Lymecycline EP Impurity D HCl , 4-Epianhydrotetracycline HCl )
CAS:Formula:C22H22N2O7·HClMolecular weight:426.43 36.46Cisatracurium Besilate EP Impurity H Besylate
CAS:Formula:C53H72N2O12·2C6H5O3SMolecular weight:929.16 2 157.16Fosinopril EP Impurity E (Fosinopril USP Related Compound E (Free Form), Phenyl Fosinopril)
Formula:C30H40NO7PMolecular weight:557.63(S)-Selegiline EP Impurity D ((S)-Selegiline USP Related Compound D (Free Form), (S)-N-Desmethyl Selegiline)
Formula:C12H15NMolecular weight:173.40N-Nitroso Cyclophosphamide EP Impurity C (N-Nitroso Cyclophosphamide USP Related Compound A (Free Form))
CAS:Formula:C4H8Cl2N2OMolecular weight:171.02Benazepril EP Impurity A (Benazepril USP Related Compound A (Free Form), ent-Benazepril)
CAS:Formula:C24H28N2O5Molecular weight:424.50Chlorothiazide-13C,15N2 (Hydrochlorothiazide EP Impurity A-13C,15N2)
CAS:Formula:C613CH6ClN15N2O4S2Molecular weight:298.69N-Nitroso Torasemide (Torsemide) EP Impurity D (N-Nitroso Torasemide (Torsemide) USP Related Compound B)
Formula:C17H21N5O4SMolecular weight:391.45Oxfendazole EP Impurity B-d3 (Fenbendazole Sulfone-d3)
CAS:Formula:C15H10D3N3O4SMolecular weight:334.36Rosuvastatin EP Impurity K Sodium Salt
CAS:Formula:C22H25FN3O5S·NaColor and Shape:Off-White Semi-SolidMolecular weight:462.52 22.99Clomifene (Clomiphene) EP Impurity A HCl (Clomiphene USP Related Compound A)
CAS:Formula:C26H29NO·HClMolecular weight:371.52 36.46Vitamin A EP Impurity B (Anhydro-Vitamin A, Anhydroretinol) (E Isomer)
CAS:Formula:C20H28Molecular weight:268.44Selegiline EP Impurity E-d4 HCl (D-(+)-Deprenyl-d4 HCl)
CAS:Formula:C13H13D4N·HClMolecular weight:191.31 36.46N-Nitroso Chlorcyclizine EP Impurity A-d11 (N-Nitroso Cyclizine EP Impurity A-d11, N-Nitroso Cyclizine USP Related Compound A-d11)
CAS:Formula:C5D11N3OMolecular weight:140.23Perindopril EP Impurity F-d4 (Perindopril USP Related Compound F-d4)
CAS:Formula:C19H26D4N2O4Molecular weight:354.48N-Nitroso Atomoxetine EP Impurity B (N-Nitroso (S)-Atomoxetine)
Formula:C17H20N2O2Molecular weight:284.36N-Nitroso Mesalazine (Mesalamine) EP Impurity K HCl (N-Nitroso Fentanyl EP Impurity F HCl, N-Nitroso Aniline HCl)
CAS:Formula:C8H8N2O5SMolecular weight:244.22Buspirone EP Impurity G (Buspirone USP Related Compound G)
CAS:Formula:C12H14N6Molecular weight:242.29Cefepime EP Impurity E (Cefepime USP Related Compound E (Free Form))
CAS:Formula:C13H19N3O3SMolecular weight:297.38Riociguat EP Impurity A-d4 (N-Desmethyl Riociguat-d4)
CAS:Formula:C19H13D4FN8O2Molecular weight:412.42




