
European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents
European Pharmacopoeia (EP) solutions and reagents ensure that pharmaceutical products meet the high-quality standards set by the European Union. These solutions are critical in testing the purity, potency, and quality of drugs. CymitQuimica offers a comprehensive range of Ph. Eur.-compliant solutions and reagents, supporting pharmaceutical research and quality control processes.
Found 9853 products of "European Pharmacopoeia (EP) (Ph. Eur.) Solutions and Reagents"
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Reagecon pH 4.60 Acetate Buffer Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.3)
Reagecon’s pH 4.6 Acetate 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 traceableColor and Shape: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 traceableColor and Shape:LiquidReagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix Method A Reference Solution in n-Heptane according to European Pharmacopoeia (EP) Chapter 2.4.22, Table 3
CAS:This Reagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix is a ready to use product that is used either as a calibrant or analytical control solution for a variety of gas and liquid chromatography methods that include GC; GC-MS; HPLC and LC-MS. This product can also be used to validate appropriate test methods or qualify an instrument in a regulated industry. - The identity of each standard is verified using a high performance calibrated Gas Chromatograph Mass Spectrometer (GC-MS Instrument). The mass spectrum of each of the analytes is confirmed by comparison with the National Institute of Standards and Technology (NIST) mass spectral library. - The esterification of fatty acids is an important tool for both characterising fats and oils and for determining the total fat content in foods and foodstuffs. It is also an important measurement for the assessing of quality and purity of biofuels. Description | Concentration: - Methyl Myristate: 10% w/w. - Methyl Palmitate: 15% w/w. - Methyl Stearate: 20% w/w. - Methyl Arachidate: 20% w/w. - Methyl Oleate: 10% w/w. - Methyl Eicosenoate: 5% w/w. - Methyl Behenate: 10% w/w. - Methyl Linocerate: 10% w/w.Color and Shape:LiquidReagecon 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.Color and Shape: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 traceableColor and Shape: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.Color and Shape:LiquidReagecon 1330 µs/cm Conductivity and Resistivity at 20°C according to European Pharmacopoeia (EP)
Reagecon's Conductivity Standard at 20°C is tested and NIST traceable. The product is aqueous based, non-hazardous and accurate to a specification of ± 1%. The product because it is aqueous based, has a low temperature coefficient of variation and guaranteed stability throughout its entire shelf life, even after opening the bottle. This product is formulated, specified and manufactured in compliance with EP requirements. - NIST traceable - This conductivity standard is aqueous based, thereby eliminating any errors attributable to matrix mismatch. Each bottle is supplied with a comprehensive Certificate of Analysis and has a table of conductivity variation with temperature printed on the product label. The low temperature coefficient of variation, reduces measurement errors and enables non-temperature controlled use - High accuracy ± 1% at 20°C, enables the standards to be used as calibrators and/or controls, in accordance with the most exacting requirements - Guaranteed stability throughout entire shelf life, even after opening the bottle, eliminates the need to open a fresh bottle of standard every time it is usedColor and Shape:LiquidReagecon Potassium Phosphate pH 6.8 Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Potassium Phosphate pH 6.8 Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Ammonium Carbonate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ammonium Carbonate 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), 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. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Concentrate to make Zinc (Zn) 100ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Zinc (Zn) 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.Color and Shape:LiquidReagecon Hydrochloric Acid 3M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 3M 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.Color and Shape:LiquidReagecon 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.Color and Shape:LiquidReagecon Tetramethylammonium Hydroxide Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Tetramethylammonium Hydroxide 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), use in materials for the manufacture of containers (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.Color and Shape: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.Color and Shape: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.Color and Shape: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 traceableColor and Shape: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.Color and Shape:LiquidReagecon Mordant Black 11 Triturate according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Mordant Black 11 Triturate is a high quality Indicator Solution produced from the highest quality raw materials and manufactured and tested under rigorous conditions. For manual titrations; indicator titrant or analyte change colour and this colour change is by far the most important method of end point detection, in such titrations. A high quality indicator solution such as Reagecon's facilitates end point detection, in a clear and unambiguous manner and is an imperative for accurate manual titrimetry.Color and Shape: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.Color and Shape:LiquidReagecon Hydrochloric Acid R1 according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Controlled ProductReagecon Hydrochloric Acid R1 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 heavy metals (2.4.8), 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.Color and Shape:LiquidReagecon Methyl Red mixed Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Red 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.Color and Shape:LiquidReagecon Hydrochloric Acid 6M according to European Pharmacopoeia (EP) Chapter 4 (4.2.2)
Reagecon's Hydrochloric Acid 6M is a fully factorised, high purity, stable product, developed and tested for titrations. This Analytical Volumetric Solution, also called titrant, standard titrant or standard solution, is tested to a specification of ± 0.2%. It is a reagent of known concentration, that is dispensed from a burette or other dispensing apparatus to a sample (analyte), until a reaction between the two liquids is judged to be complete. The product may be used for manual titrations, or more commonly automatic titrations, to determine the end points by detection of any of several properties as detailed in several EP monographs. - NIST traceable - Titration is a rapid, economical and versatile analytical tool. This Reagecon titrant is accurate, stable, reproducible and fully factorised. Titrations performed with this product, exhibit defined stochiometry, are quantitative, establish an equilibrium that is definitive and fast and provide unambiguous results. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Potassium Iodide and Starch Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Potassium Iodide and Starch Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator as outlined in individual EP product monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon 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 spectrophotometerColor and Shape:LiquidReagecon B1 to B9 Colour Reference Set according to European Pharmacopoeia (EP)
Reagecon’s B1 to B9 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 spectrophotometerColor and Shape: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.Color and Shape: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 traceableColor and Shape:LiquidReagecon Phenolphthalein Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phenolphthalein Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as an indicator In volumetric titrations, plus as an indicator of pH change as outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape: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.Color and Shape:LiquidReagecon Methyl Red Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon's Methyl Red 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.Color and Shape:LiquidReagecon pH 1.68 Buffer Solution at 25°C according to European Pharmacopoeia (EP)
Reagecon's pH Buffer Solution at 25°C is tested by an ISO 17025 Accredited Test Method (A2LA Ref: 6739.03) and NIST traceable; has guaranteed stability throughout its entire shelf life; even after opening the bottle. The product is developed; formulated and specified in accordance with EP requirements. - NIST traceableColor and Shape:LiquidReagecon Concentrate to make Aluminium (Al) 100ppm Standard Solution according to European Pharmacopoeia Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Aluminium (Al) 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.Color and Shape:LiquidReagecon Aluminium (Al) 200ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Aluminium (Al) 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.Color and Shape:LiquidEPO/Erythropoietin Protein, Human, Recombinant (hFc)
<p>EPO/Erythropoietin Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag.</p>Purity:SDS-PAGE: 96.3%; SEC-HPLC: 97.2% - SDS-PAGE: 96.3%; SEC-HPLC: 97.2%Color and Shape:Lyophilized PowderMolecular weight:45.1 kDa (predicted)Diethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Formula:C6H14O3Purity:≥ 99.900%Color and Shape:Colourless liquidMolecular weight:134.18EPO/Erythropoietin Protein, Human, Recombinant
<p>Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.</p>Color and Shape:Lyophilized PowderMolecular weight:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.Oxfendazole EP Impurity B-d3 (Fenbendazole Sulfone-d3)
CAS:Formula:C15H10D3N3O4SMolecular weight:334.36Isotretinoin EP Impurity H-d6 (4-Oxo-13-cis-Retinoic Acid-d6)
CAS:Formula:C20H20D6O3Molecular weight:320.46(+)-trans-Limonene Oxide ((+)-trans-Terpin EP Impurity C Oxide)
CAS:Formula:C10H16OMolecular weight:152.24Pantoprazole EP Impurity B-d6 (Pantoprazole USP Related Compound B-d6, Pantoprazole Sulfide-d6)
CAS:Formula:C16H9D6F2N3O3SMolecular weight:373.41Atropine EP Impurity E-13C-d3 (7-β-Hydroxyhyoscyamine-13C-d3)
Formula:C1613CH20D3NO4Molecular weight:309.38Fosinopril EP Impurity C (Fosinopril USP Related Compound C)
Formula:C30H45NO7P·NaMolecular weight:562.67 22.99Sevoflurane EP Impurity B (Sevoflurane USP Related Compound B)
CAS:Formula:C4H4F6OMolecular weight:182.07N-Nitroso Nicardipine EP Impurity C (N-Nitroso Nicardipine USP Related Compound C, N-Nitroso Nitrendipine EP Impurity B)
Formula:C17H17N3O7Molecular weight:375.34Desogestrel EP Impurity C-d2 (Desogestrel USP Related Compound D-d2)
CAS:Formula:C20H26D2OMolecular weight:286.46Methylprednisolone Acetate EP Impurity F
CAS:Formula:C24H30O5Color and Shape:White To Off-White SolidMolecular weight:398.50Almotriptan EP Impurity D (Almotriptan USP Related Compound B)
CAS:Formula:C15H21N3O2SC4H4O4Molecular weight:307.41 1/2*116.07N-Nitroso-Tetracaine EP Impurity A-d4 (N-Nitroso-Benzylpenicillin (Procaine) EP Impurity A-d4, N-Nitroso-4-Aminobenzoic Acid-d4)
Formula:C7H2D4N2O3Molecular weight:170.16Megestrol Acetate-13C2-d3 (Medroxyprogesterone Acetate EP Impurity G-13C2-d3)
Formula:C2213C2H29D3O4Molecular weight:389.51Dexamethasone Acetate-13C3 (Dexamethasone EP Impurity G-13C3, Betamethasone Acetate EP Impurity B-13C3)
CAS:Formula:C2113C3H31FO6Molecular weight:437.48N-Nitroso Verapamil EP Impurity J-d7 (N-Nitroso N-Desmethyl Verapamil-d7, N-Nitroso Norverapamil-d7)
Formula:C26H28D7N3O5Molecular weight:476.62N2-Nitroso Benzylpenicillin (Benzathine) EP Impurity C (N2-Nitroso Benzylpenicilloic Acids Benzathine)
Formula:C32H37N5O5SMolecular weight:603.74Clonidine EP Impurity B-d4 (Clonidine USP Related Compound A-d4)
Formula:C11H7D4Cl2N3OMolecular weight:276.15Risperidone EP Impurity C N1-Oxide (Paliperidone N1-Oxide)
Formula:C23H27FN4O4Molecular weight:442.49Riboflavin Sodium Phosphate EP Impurity A (Riboflavin-3’, 4’-Diphosphate)
CAS:Formula:C17H22N4O12P2Molecular weight:536.33rac-Levonorgestrel EP Impurity I (10-β-Hydroxylevonorgestrel)
CAS:Formula:C21H28O3Molecular weight:328.45Calcium sulfate dihydrate, BP, Ph. Eur. grade
CAS:Formula:CaSO4·2H2OPurity:(Titration) 98.0 - 102.0 % (CaSO4 · 2H2O)Color and Shape:White or almost white fine powderMolecular weight:172.17N-Nitroso Sertraline EP Impurity D (Mixture of Two Enantiomers)
Formula:C17H17ClN2OMolecular weight:300.79Rotigotine EP Impurity G (Rotigotine USP Related Compound G (Free Form))
CAS:Formula:C22H25NOS2Molecular weight:383.57Ziprasidone EP Impurity D (Ziprasidone USP Related Compound C)
CAS:Formula:C42H40Cl2N8O3S2Molecular weight:839.87N-Nitroso Trospium Chloride EP Impurity B (N-Nitroso Trospium Chloride USP Related Compound B)
Formula:C21H22N2O4Molecular weight:366.42(S)-(-)-Limonene-13C-d2 ((S)-(-)-Terpin EP Impurity C-13C-d2)
CAS:Formula:CC9H14D2Molecular weight:139.24N-Nitroso Chlorcyclizine EP Impurity A-d11 (N-Nitroso Cyclizine EP Impurity A-d11, N-Nitroso Cyclizine USP Related Compound A-d11)
CAS:Formula:C5D11N3OMolecular weight:140.23Perindopril EP Impurity F-d4 (Perindopril USP Related Compound F-d4)
CAS:Formula:C19H26D4N2O4Molecular weight:354.48Lansoprazole EP Impurity B-d4 (Lansoprazole USP Related Compound A-d4, Lansoprazole Sulfone-d4)
CAS:Formula:C16H10D4F3N3O3SMolecular weight:389.39Estradiol Hemihydrate EP Impurity D-13C2 (δ-9(11)-Estradiol-13C2)
CAS:Formula:C1613C2H22O2Molecular weight:272.36N-Nitroso Oxcarbazepine EP Impurity D (N-Nitroso Dibenzazepinodione)
Formula:C14H8N2O3Molecular weight:252.23Vancomycin EP Impurity L ([L-α-Asp3] Vancomycin B)
CAS:Formula:C66H74Cl2N8O25Molecular weight:1450.25Flubendazole, Ph. Eur. grade
CAS:Formula:C16H12FN3O3Purity:99.0 - 101.0 % (dried basis)Color and Shape:White to almost white powderMolecular weight:313.28Methotrexate EP Impurity E-13C-d3 (Methotrexate USP Related Compound E-13C-d3)
Formula:C1413CH12D3N7O2Molecular weight:329.34C5-Nitroso Uridine (C5-Nitroso Adenosine EP Impurity F, C5-Nitroso Cytarabine EP Impurity B)
CAS:Formula:C9H11N3O7Molecular weight:273.20C5-Nitroso Cytosine (C5-Nitroso Gemcitabine EP Impurity A, C5-Nitroso Lamivudine EP Impurity E, C5-Nitroso Cytarabine EP Impurity C)
Formula:C4H4N4O2Molecular weight:140.10Di-N-Nitroso Cyclophosphamide EP Impurity E (Di-N-Nitroso Cyclophosphamide USP Related Compound D)
Formula:C7H16ClN4O6PMolecular weight:318.65N1-Nitroso Theophylline (N1-Nitroso Dimenhydrinate EP Impurity A, N1-Nitroso Diprophylline EP Impurity B)
Formula:C7H7N5O3Molecular weight:209.17Triflusal EP Impurity B-13C6 (Desacetyl Triflusalic Acid-13C6)
CAS:Formula:C213C6H5F3O3Molecular weight:212.07Fosinopril EP Impurity F (Fosinopril USP Related Compound F)
Formula:C29H44NO7PMolecular weight:549.65Orbifloxacin EP Impurity E
CAS:Formula:C6H14N2Color and Shape:White To Off-White SolidMolecular weight:114.19




