
Soluzioni e reagenti della Farmacopea europea (EP)
Le soluzioni e i reagenti della Farmacopea Europea (Ph. Eur.) garantiscono che i prodotti farmaceutici soddisfino gli elevati standard di qualità stabiliti dall'Unione Europea. Queste soluzioni sono fondamentali per testare la purezza, la potenza e la qualità dei farmaci. Presso CymitQuimica, offriamo una gamma completa di soluzioni e reagenti conformi alla Ph. Eur., a supporto della ricerca farmaceutica e dei processi di controllo qualità.
Trovati 9885 prodotti di "Soluzioni e reagenti della Farmacopea europea (EP)"
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Reagecon Perchloric Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Perchloric Acid Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma: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.Colore e forma:LiquidReagecon Iodoplatinate Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Iodoplatinate Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma: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.Colore e forma: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.Colore e forma: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 spectrophotometerColore e forma:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.1N Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Colore e forma:LiquidReagecon Potassium Phosphate pH 7.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 7.5 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 250ml in volume in each bottle and the contents of each bottle can be diluted to produce 10L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 250ml of solution, each 250ml bottle is diluted to give 10L of ready to use Dissolution Medium.Colore e forma:LiquidReagecon Potassium Pyroantimonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Pyroantimonate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma:LiquidReagecon Y4 Yellow Colour Reference Solution according to European Pharmacopoeia (EP)
Reagecon's Y4 Yellow Colour Reference Solution is formulated as a reference solution for the examination of the degree of colouration of liquids in accordance with the European Pharmacopoeia Chapter 2.2.2. This product is produced by combining Reagecon's Primary Colour Solutions. - This Reference Colour Solution is a ready to use coloration standard presented in high quality, tamper evident bottles for use as a calibration and/or quality control standard. It is prepared by combining Reagecon Primary Colour Solutions. - Concentration verified using a high performance spectrophotometer.Colore e forma:LiquidReagecon Crystal Violet Solution (non-aqueous indicator) according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Crystal Violet Solution (non-aqueous indicator) is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Colore e forma:LiquidReagecon Carbon Dioxide Free Water according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Carbon Dioxide Free Water is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include the preparation of other reagents (4.1.1) and used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma:LiquidReagecon pH 7.41 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColore e forma: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.Colore e forma: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.Colore e forma:LiquidReagecon pH 3.50 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 3.6 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 traceableColore e forma: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.Colore e forma: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.Colore e forma:LiquidReagecon Acetate Buffer pH 4.5 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 230.85ml in volume in each bottle and the contents of each bottle can be diluted to produce 6L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 230.85ml of solution, each 230.85ml bottle is diluted to give 6L of ready to use Dissolution Medium.Colore e forma:LiquidReagecon Zinc Sulphate 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Zinc 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.Colore e forma:LiquidReagecon Silver Nitrate R1 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Silver Nitrate R1 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.Colore e forma: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.Colore e forma: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.Colore e forma:LiquidReagecon Copper Sulphate 0.02M according to European Pharmacopoeia (EP)
Reagecon's Copper Sulphate 0.02M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon AVL 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.Colore e forma:LiquidReagecon Potassium Iodide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use in the identification reactions of ions and functional groups (2.3.1) and used as a reagent in the performance of tests outlined in several EP monographs. - NIST traceable - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma:LiquidReagecon Potassium Iodobismuthate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodobismuthate R2 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.Colore e forma: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.Colore e forma:LiquidReagecon Bromocresol Purple 0.04% Indicator Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromocresol Purple 0.04% Indicator Solution is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Colore e forma: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.Colore e forma:LiquidReagecon Potassium Ferrocyanide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Ferrocyanide 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.Colore e forma:LiquidReagecon Starch Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Starch 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.Colore e forma:LiquidReagecon Lead (Pb) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Lead (Pb) 0.1% Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Colore e forma:LiquidReagecon Sodium Nitroprusside 100g/L in Dilute Sulphuric Acid according to European Pharmacopoeia (EP)
Reagecon Sodium Nitroprusside 100 g/L Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. Used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma:LiquidReagecon Potassium Phosphate pH 6.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 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.Colore e forma:LiquidReagecon pH 6.00 Phosphate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 6.0 Phosphate Buffer Solution is specified for use in individual European Pharmacopoeia (EP) Monographs. It is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. - NIST traceableColore e forma: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.Colore e forma:LiquidReagecon Hydrochloric Acid 1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.1%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma: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.Colore e forma:LiquidReagecon Sodium Hydroxide 0.1M Ethanolic according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Sodium Hydroxide 0.1M Ethanolic 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.Colore e forma:LiquidReagecon Acetate Buffer pH 4.5 and 1.0% Sodium Dodecyl Sulphate Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Acetate Buffer pH 4.5 and 1.0% Sodium Dodecyl Sulphate Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Colore e forma:LiquidReagecon Hydrochloric Acid 0.1N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Hydrochloric Acid 0.1N Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Colore e forma:LiquidReagecon Concentrate to make Antimony (Sb) 1000ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Antimony (Sb) 1000ppm Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Colore e forma:LiquidReagecon Sulfomolybdic R3 Reagent according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sulfomolybdic R3 Reagent is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. Used as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma:LiquidReagecon Potassium Phosphate pH 5.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 5.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 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.Colore e forma:LiquidReagecon Concentrate to make Sodium (Na) 200ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Sodium (Na) 200ppm 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.Colore e forma:LiquidReagecon Concentrate to make Magnesium (Mg) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Magnesium (Mg) 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.Colore e forma: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.Colore e forma: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.Colore e forma:LiquidReagecon Tetrabutylammonium Hydroxide 0.1M in 2-propanol according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Tetrabutylammonium Hydroxide 0.1M in 2-propanol 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.Colore e forma:LiquidReagecon Bromocresol Green Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Bromocresol Green 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.Colore e forma:LiquidReagecon Anisaldehyde Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Anisaldehyde 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.Colore e forma:LiquidReagecon Perchloric Acid 0.1M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Perchloric Acid 0.1M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Colore e forma: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.Colore e forma:LiquidReagecon Potassium Phosphate pH 6.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 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.Colore e forma: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.Colore e forma: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 traceableColore e forma:LiquidEPO/Erythropoietin Protein, Human, Recombinant
Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.Purezza:> 95% as determined by Bis-Tris PAGE > 95% as determined by HPLC - > 95% as determined by Bis-Tris PAGE > 95% as determined by HPLCColore e forma:Lyophilized PowderPeso molecolare:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.EPO/Erythropoietin Protein, Human, Recombinant (hFc)
<p>EPO/Erythropoietin Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag.</p>Purezza:SDS-PAGE: 96.3%; SEC-HPLC: 97.2% - SDS-PAGE: 96.3%; SEC-HPLC: 97.2%Colore e forma:Lyophilized PowderPeso molecolare:45.1 kDa (predicted)Diethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Formula:C6H14O3Purezza:≥ 99.900%Colore e forma:Colourless liquidPeso molecolare:134.18N-Nitroso Chlorcyclizine EP Impurity A-d11 (N-Nitroso Cyclizine EP Impurity A-d11, N-Nitroso Cyclizine USP Related Compound A-d11)
CAS:Formula:C5D11N3OPeso molecolare:140.23Ref: 4Z-C-332005
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-I-3745
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-V-0440
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN2-Nitroso Folinic Acid (N2-Nitroso (6RS)-Calcium Levofolinate EP Impurity H, N2-Nitroso Leucovorin)
Formula:C20H22N8O8Peso molecolare:502.44Ref: 4Z-F-068042
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN-Nitroso Omeprazole EP Impurity A (N-Nitroso Omeprazole USP Related Compound B, N-Nitroso Esomeprazole EP Impurity A)
Formula:C8H7N3O2SPeso molecolare:209.22Ref: 4Z-O-02160
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-I-057070
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-P-0275
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-A-155059
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-I-108002
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-A-2678
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-L-126003
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-E-158003
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN-Nitroso Dicloxacillin Sodium EP Impurity B (Mixture of Diastereomers)
Formula:C18H18Cl2N4O5SPeso molecolare:473.33Ref: 4Z-D-6813
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN1,N2-Dinitroso Lacosamide EP Impurity B (N1,N2-Dinitroso Lacosamide USP Related Compound B, N1,N2-Dinitroso rac-O-Acetyl Lacosamide)
Formula:C14H16N4O6Peso molecolare:336.30Ref: 4Z-L-2879
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-F-534
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-B-086021
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-G-044001
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-U-067
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-D-4530
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaGlutathione EP Impurity A Trifluoroacetate
CAS:Formula:C5H10N2O3S·C2HF3O2Peso molecolare:178.21 114.02Ref: 4Z-PG-2540
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN1-Nitroso Lacosamide EP Impurity F (S-Isomer) (N1-Nitroso Lacosamide USP Related Compound F (S-Isomer))
Formula:C12H15N3O4Peso molecolare:265.27Ref: 4Z-L-2871
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-L-112020
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-G-407
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-A-155060
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-L-112017
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-L-112021
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-L-112015
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-B-4921
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta(6R,2'S)-Folinic Acid (Calcium Levofolinate EP Impurity H, (6R,2'S)-Leucovorin)
CAS:Formula:C20H23N7O7Peso molecolare:473.45Ref: 4Z-F-068043
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaSevoflurane EP Impurity B (Sevoflurane USP Related Compound B)
CAS:Formula:C4H4F6OPeso molecolare:182.07Ref: 4Z-S-093003
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-N-095003
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaSevoflurane EP Impurity A (Sevoflurane USP Related Compound A)
CAS:Formula:C4H2F6OPeso molecolare:180.05Ref: 4Z-S-093002
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-M-739
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-M-7314
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN-Nitroso Tetracaine EP Impurity C (N-Nitroso Tetracaine USP Related Compound C)
Formula:C12H16N2O3Peso molecolare:236.27Ref: 4Z-T-1939
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaAmiodarone EP Impurity G-d4
CAS:Formula:C26H27D4I2NO4Colore e forma:White To Off-White SolidPeso molecolare:679.37Ref: 4Z-A-0742
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-B-0110
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-E-2225
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-V-037001
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaRef: 4Z-W-0128
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaN-Nitroso Trospium Chloride EP Impurity B (N-Nitroso Trospium Chloride USP Related Compound B)
Formula:C21H22N2O4Peso molecolare:366.42Ref: 4Z-T-2215
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta




