
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 9878 productos de "Soluciones y reactivos de la farmacopea europea (EP) (Ph. Eur.)"
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Reagecon Congo Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Congo Red Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Forma y color:LiquidReagecon 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.Forma y color:LiquidReagecon Hydrochloric Acid Dilute R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Hydrochloric Acid Dilute R1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon BY5 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY5 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerForma y color:LiquidReagecon 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 spectrophotometerForma y color:LiquidReagecon Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Gastric Fluid without enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 230.85ml in volume in each bottle and the contents of each bottle can be diluted to produce 6L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 230.85ml of solution, each 230.85ml bottle is diluted to give 6L of ready to use Dissolution Medium.Forma y color:LiquidReagecon Potassium 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 Concentrate to make Phosphate (PO₄) 5ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Phosphate (PO?) 5ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon Potassium Hydrogen Phthalate 0.2M according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Hydrogen Phthalate 0.2M is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include as a component of buffer solutions (4.1.3). - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon pH 4.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableForma y color:LiquidReagecon Acetate Buffer pH 4.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Forma y color:LiquidReagecon B8 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B8 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon pH 10.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableForma y color:LiquidReagecon 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 Fatty Acid Methyl Ester (FAME) 6 Compound Mix according to European Pharmacopoeia (EP) Chapter 2.4.22-1 Neat
This Reagecon Fatty Acid Methyl Ester (FAME) 6 Compound Mix is presented in Neat form (solid). This presentation confers on the user advantages, that include flexibility in terms of matrix type and concentration of standard prepared, easier storage, safer handling and extended shelf life. The product can be used either as a calibrant or analytical control solution for a variety of gas and liquid chromatography methods that include GC, GC-MS, HPLC and LC-MS. This product can also be used to validate appropriate test methods or qualify an instrument in a regulated industry. The esterification of fatty acids is an important tool for both characterising fats and oils and for determining the total fat content in foods and foodstuffs. It is also an important measurement for the assessing of quality and purity of biofuels. Description | Concentration: - Methyl Laurate: 5% w/w. - Methyl Myristate: 5% w/w. - Methyl Palmitate: 10% w/w. - Methyl Stearate: 20% w/w. - Methyl Arachidate: 40% w/w. - Methyl Oleate: 20% w/w.Forma y color:SolidReagecon HCL Dilution Matrix (10g/L HCl) according to European Pharmacopoeia (EP)
Reagecon’s HCl Dilution Matrix (10g/L HCl) is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.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 Barium Hydroxide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Barium Hydroxide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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.Forma y color: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.Forma y color:LiquidReagecon Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 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 Acetic Anhydride R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Acetic Anhydride R1 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in determination of Hydroxly value (2.5.3) and used as a reagent in the performance of tests outlined in several EP monographs. - 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 Picric Acid R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Picric Acid R1 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Cupri-Citric Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Cupri-Citric Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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 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 Ninhydrin Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ninhydrin Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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 pH 8.50 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 8.5 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableForma y color:LiquidReagecon Potassium Tetraiodomercurate Solution Alkaline Part B according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
For Potassium Tetraiodomercurate Solution Alkaline 1071600 both parts 1071600-A and 1071600-B are required Reagecon Potassium Tetraiodomercurate Solution Alkaline Part B is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Forma y color:LiquidReagecon Potassium Phosphate pH 6.0 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 6.0 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 Y5 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y5 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 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.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 Potassium Phosphate pH 7.2 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 7.2 Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Forma y color:LiquidReagecon GY7 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY7 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerForma y color:LiquidReagecon Concentrate to make Chloride (Cl) 8ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Chloride (Cl) 8ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon Concentrate to make Lead (Pb) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Lead (Pb) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon BY6 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s BY6 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 Concentrate to make Potassium (K) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Potassium (K) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.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 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 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.Forma y color:LiquidReagecon GY4 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s GY4 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 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 Concentrate to make Chloride (Cl) 5ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2)
Reagecon's Concentrate to make Chloride (Cl) 5ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon Potassium Permanganate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Producto controladoReagecon Potassium Permanganate 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 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.Forma y color:LiquidReagecon Hydrochloric Acid 0.1N and 1.0% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.1N and 1.0% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Forma y color:LiquidReagecon pH 4.01 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableForma y color:LiquidReagecon 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.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 Ferroin according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ferroin is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator for manual titrations as outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Forma y color:LiquidReagecon Standard Colour Solution BY (Brownish Yellow) according to European Pharmacopoeia (EP) Chapter 2.2.2
CAS:Reagecon's Standard Colour Solution BY (Brownish Yellow) is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Standard Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Sodium Hydroxide Strong Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sodium Hydroxide Strong Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1), a component of buffer solutions (4.1.3), use in identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.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 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 spectrophotometerForma 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 B6 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B6 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Selenium (Se) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Selenium (Se) 100ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Forma y color:LiquidReagecon B9 Brown Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s B9 Brown Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Potassium Dichromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Dichromate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon pH 3.00 Citrate 0.25M Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 3.0 Citrate 0.25M 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.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 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.Forma y color:LiquidReagecon Molybdovanadic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Molybdovanadic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Methoxyphenylacetic Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Methoxyphenylacetic Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible.Forma y color:LiquidReagecon Potassium Hydroxide 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Hydroxide 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Mercuric Bromide Paper according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Mercuric Bromide Paper is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in limit test for arsenic (2.4.2). - 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 Zinc Chloride 0.05M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Zinc Chloride 0.05M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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.Forma y color: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.Forma y color:LiquidReagecon Cupri-Tartaric Solution 1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:For Cupri-tartaric Solution 1023300 both parts 1023300-A and 1023300-B are required Reagecon's Cupri-Tartaric Solution 1 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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 Acetic Acid Dilute (12%) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Acetic Acid Dilute (12%) 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 5.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 5.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 384ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 384ml of solution, each 384ml bottle is diluted to give 10L of ready to use Dissolution Medium.Forma y color:LiquidReagecon 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.Forma y color:LiquidReagecon Y6 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y6 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Forma y color:LiquidReagecon Hydrochloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Potassium Bromate 0.033M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Potassium Bromate 0.033M 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 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 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 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 Ammonium Molybdate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonium Molybdate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in determination of Hydroxly value (2.5.3) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color: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.Forma y color:LiquidReagecon Cupri-Tartaric Solution 2 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
For Cupri-tartaric Solution 1023300 both parts 1023300-A and 1023300-B are required Reagecon's Cupri-Tartaric Solution 2 is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Y1 to Y7 Colour Reference Set according to European Pharmacopoeia (EP)
Reagecon’s Y1 to Y7 Colour Reference Set is formulated as a set of reference solutions for the examination of the degree of colour of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. These products are produced by combining Reagecon Primary Colour Solutions - Concentration verified using a high performance spectrophotometerForma y color:LiquidReagecon Silver Nitrate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Silver Nitrate R2 Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Biuret Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Biuret Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon Potassium Chromate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Potassium Chromate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator for titrations in individual EP product 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 Simulated Gastric Fluid without Enzyme Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Simulated Gastric Fluid without Enzyme Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Forma y color:LiquidReagecon R4 Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon’s R4 Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometerForma y color:LiquidReagecon Zinc Chloride Formic Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Zinc Chloride Formic Acid Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1). - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:LiquidReagecon 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 Ammonium Cerium Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Ammonium Cerium Sulphate 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Forma y color:Liquid

