
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"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Reagecon Potassium Tetraiodomercurate Solution Alkaline Part A 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 A 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 Phenylhydrazine Hydrochloride Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Phenylhydrazine Hydrochloride 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 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 961.5ml in volume in each bottle and the contents of each bottle can be diluted to produce 25L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 6 bottles, each of which has a volume of 961.5ml of solution, each 961.5ml bottle is diluted to give 25L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Potassium Phosphate pH 6.8 R Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP)
Reagecon's Potassium Phosphate pH 6.8 R Dissolution Media is a ready to use solution, specifically formulated to perform dissolution studies on solid form pharmaceutical preparations. The product is prepared in accordance with relevant Pharmacopoeia requirements, without any deviations in materials or methodology from the Pharmacopoeia methods. - The product has the reported accuracy and guaranteed stability of 2 years.Color and Shape:LiquidReagecon BRP Indicator Solution according to European Pharmacopoeia (EP)
Reagecon's BRP 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.Color and Shape:LiquidReagecon Ferric Ammonium Sulphate R2 Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Ferric Ammonium Sulphate R2 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. - 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 Standard Colour Solution GY (Greenish Yellow) according to European Pharmacopoeia (EP) Chapter 2.2.2
Reagecon's Standard Colour Solution GY (Greenish 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.Color and Shape:LiquidReagecon Standard Colour Solution R (Red) according to European Pharmacopoeia (EP) Chapter 2.2.2
CAS:Reagecon's Standard Colour Solution R (Red) 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.Color and Shape:LiquidReagecon Zinc Acetate Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Zinc Acetate Solution is a high purity stable product developed and tested for European Pharmacopoeia (EP) applications. These include use as a reagent in the performance of tests outlined in several EP monographs. - This Reagecon EP reagent is accurate, stable and reproducible. Stability is proven (either opened or unopened) for the shelf life of this product.Color and Shape:LiquidReagecon Sodium Hypochlorite Strong Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
CAS:Reagecon Sodium Hypochlorite Strong 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 Concentrate to make Ammonium (NH4) 1ppm Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Concentrate to make Ammonium (NH4) 1ppm 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 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.Color and Shape: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 spectrophotometerColor and Shape: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.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 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 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 traceableColor and Shape:LiquidReagecon Hydrochloric Acid 0.01N Dissolution Media in accordance to United States (USP) and European Pharmacopoeias (EP) Concentrate
Reagecon's Hydrochloric Acid 0.01N Dissolution Media Concentrate is presented in concentrate form. This concentrate measures 230.85ml in volume in each bottle and the contents of each bottle can be diluted to produce 6L of working solution in water. This diluted volume is the working Dissolution Medium. The product is prepared and when diluted can be used in accordance with relevant pharmacopoeia requirements. - This product is presented as a concentrate in order to facilitate easy shipping, storage and handling. - The pack contains 12 bottles, each of which has a volume of 230.85ml of solution, each 230.85ml bottle is diluted to give 6L of ready to use Dissolution Medium.Color and Shape:LiquidReagecon Picric Acid Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Picric 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.Color and Shape:LiquidReagecon Copper (Cu) 0.1% Standard Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.2) Limit Test
Reagecon's Copper (Cu) 0.1% Standard Solution is used in the preparation of other reagents and as specified in individual monographs. This product is manufactured gravimetrically using the mass balance approach: 100% less the sum of all impurities (w/w). Prior to bottling; the final product is tested and verified using ICP-MS and is reported using the gravimetric result; corrected for density to a specification of ± 0.2%. Reagecon hold ISO 17025 accreditation (A2LA Ref: 6739.02) for calibration of laboratory balances. - This product is produced in a highly controlled cleanroom (ISO 7) environment, using ultra-pure water (specially treated for the production of mass spectroscopy standards). The titrimetry and spectroscopy are controlled and calibrated using separate standards, so the product comes with two layers of traceability including NIST Standards where available. All of the uncertainties of measurement for this product are calculated according to Eurachem/CITAC guidelines and reported as expanded uncertainties at the 95% confidence level.Color and Shape:LiquidReagecon 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 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.Color and Shape: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.Color and Shape: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.Color and Shape: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.Color and Shape: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.Color and Shape:LiquidReagecon Hydrochloric Acid Dilute according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Hydrochloric Acid Dilute 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 Sulphuric Acid Dilute Solution according to European Pharmacopoeia (EP) Chapter 4 (4.1.1)
Reagecon Sulphuric Acid Dilute 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. - 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 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.Color and Shape: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.Color and Shape:SolidReagecon Fatty Acid Methyl Ester (FAME) 5 Compound Mix according to European Pharmacopoeia (EP) Chapter 2.4.22-2 Neat
This Reagecon Fatty Acid Methyl Ester (FAME) 5 Compound Mix is presented in Neat form (liquid). 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 Caproate: 10% w/w. - Methyl Caprylate: 10% w/w. - Methyl Caprate: 20% w/w. - Methyl Laurate: 20% w/w. - Methyl Myristate: 40% w/w.Color and Shape:LiquidReagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix according to European Pharmacopoeia (EP) Chapter 2.4.22-3 Neat
This Reagecon Fatty Acid Methyl Ester (FAME) 8 Compound Mix is presented in Neat form (solid). This presentation confers on the user advantages, that include flexibility in terms of matrix type and concentration of standard prepared, easier storage, safer handling and extended shelf life. The product can be used either as a calibrant or analytical control solution for a variety of gas and liquid chromatography methods that include GC, GC-MS, HPLC and LC-MS. This product can also be used to validate appropriate test methods or qualify an instrument in a regulated industry. The esterification of fatty acids is an important tool for both characterising fats and oils and for determining the total fat content in foods and foodstuffs. It is also an important measurement for the assessing of quality and purity of biofuels. Description | Concentration: - Methyl Myristate: 5% w/w. - Methyl Palmitate: 10% w/w. - Methyl Stearate: 15% w/w. - Methyl Arachidate: 20% w/w. - Methyl Oleate: 20% w/w. - Methyl Eicosenoate: 10% w/w. - Methyl Behenate: 10% w/w. - Methyl Lignocerate: 10% w/w.Color and Shape:SolidEPO/Erythropoietin Protein, Human, Recombinant (hFc)
<p>EPO/Erythropoietin Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag.</p>Purity:SDS-PAGE: 96.3%; SEC-HPLC: 97.2% - SDS-PAGE: 96.3%; SEC-HPLC: 97.2%Color and Shape:Lyophilized PowderMolecular weight:45.1 kDa (predicted)EPO/Erythropoietin Protein, Human, Recombinant
<p>Erythropoietin (EPO) is a circulating hormone conventionally considered to be responsible for erythropoiesis.</p>Color and Shape:Lyophilized PowderMolecular weight:18.39 kDa (predicted). Due to glycosylation, the protein migrates to 35-45 kDa based on Tris-Bis PAGE result.Diethylene glycol monoethyl ether, Ph. Eur., USP grade
CAS:Formula:C6H14O3Purity:≥ 99.900%Color and Shape:Colourless liquidMolecular weight:134.18Vitamin A EP Impurity B (Anhydro-Vitamin A, Anhydroretinol) (E Isomer)
CAS:Formula:C20H28Molecular weight:268.44Clomifene (Clomiphene) EP Impurity A HCl (Clomiphene USP Related Compound A)
CAS:Formula:C26H29NO·HClMolecular weight:371.52 36.46N-Nitroso Etodolac EP Impurity H (N-Nitroso 7-Ethyl Trypophopl)
Formula:C12H14N2O2Molecular weight:218.26Dacarbazine EP Impurity B-13C3 HCl (Dacarbazine USP Related Compound A-13C3 HCl)
CAS:Formula:C13C3H6N4O·HClMolecular weight:129.10 36.46Risedronate EP Impurity C (Risedronate USP Related Compound C)
CAS:Formula:C7H11NO6P2Molecular weight:267.11Captopril EP Impurity A-d6 (Captopril Disulfide-d6)
CAS:Formula:C18H22D6N2O6S2Molecular weight:438.59Lansoprazole EP Impurity C-d4 (Lansoprazole USP Related Compound B-d4 (Free Form), Lansoprazole Sulfide-d4)
CAS:Formula:C16H10D4F3N3OSMolecular weight:357.39Neomycin EP Impurity C (Neomycin C) TFA Salt
CAS:Formula:C23H46N6O13·xC2HF3O2Color and Shape:Off-White SolidMolecular weight:614.65 x*114.02Calcium Folinate EP Impurity I (Folitixorin) (Mixture of Diastereomers)
CAS:Formula:C20H23N7O6Molecular weight:457.45N-Nitroso Vancomycin EP Impurity D Trifluoroacetate
Formula:C59H61Cl2N9O23·C2HF3O2Molecular weight:1335.08 114.02Folinic Acid-d4 Calcium Salt ((6RS)-Calcium Levofolinate EP Impurity H-d4 Calcium Salt , Leucovorin-d4 Calcium Salt)
Formula:C20H17D4N7O7·CaMolecular weight:475.46 40.08Benazepril EP Impurity D HCl (Benazepril USP Related Compound D)
Formula:C24H34N2O5·HClMolecular weight:430.55 36.46Benazepril EP Impurity F (Benazepril USP Related Compound F)
CAS:Formula:C16H22N2O3Molecular weight:290.37N-Nitroso Lidocaine EP Impurity H (N-Nitroso Lidocaine USP Related Compound H)
Formula:C10H11ClN2O2Molecular weight:226.66Rivastigmine Hydrogen Tartrate EP Impurity E Tartrate
Formula:C13H20N2O2·C4H6O6Molecular weight:236.32 150.09Folinic Acid-d4 ((6RS)-Calcium Levofolinate EP Impurity H-d4, Leucovorin-d4)
Formula:C20H19D4N7O7Molecular weight:477.47Calcium Pantothenate EP Impurity D (Methyl Pantothenate)
CAS:Formula:C10H19NO5Molecular weight:233.26Benazepril EP Impurity E HCl (Benazepril USP Related Compound E)
CAS:Formula:C12H14N2O3·HClMolecular weight:234.26 36.46Doxepin EP Impurity C-13C-d3 HCl ((E)-Doxepin USP Related Compound C-13C-d3, Desmethyl (E)-Doxepin-13C-d3 HCl, (E)-Nordoxepin-13C-d3 HCl)
CAS:Formula:C1713CH16D3NO·HClMolecular weight:269.37 36.46N-Nitroso Promazine EP Impurity B (N-Nitroso Desmethyl Promazine)
Formula:C16H17N3OSMolecular weight:299.39Megestrol Acetate-13C-d3 (Medroxyprogesterone Acetate EP Impurity G-13C-d3)
CAS:Formula:C2313CH29D3O4Molecular weight:388.53N-Nitroso Lacosamide EP Impurity D (N-Nitroso Lacosamide USP Related Compound D (Free Form))
Formula:C11H15N3O3Molecular weight:237.26Fosinopril EP Impurity A-d5 (Fosinopril USP Related Compound A-d5, Fosinoprilat-d5)
CAS:Formula:C23H29D5NO5PMolecular weight:440.53Rabeprazole EP Impurity A-d3 (Rabeprazole USP Related Compound D-d3, Rabeprazole Sulfone-d3)
CAS:Formula:C18H18D3N3O4SMolecular weight:378.46Isotretinoin EP Impurity H-d6 (4-Oxo-13-cis-Retinoic Acid-d6)
CAS:Formula:C20H20D6O3Molecular weight:320.46N-Nitroso Meropenem EP Impurity A Disodium Salt
Formula:C17H24N4O7S·2NaMolecular weight:428.46 2*22.99Methotrexate EP Impurity C (Methotrexate USP Related Compound C)
CAS:Formula:C20H21N7O6Molecular weight:455.43Azithromycin EP Impurity B (Azithromycin B)
CAS:Formula:C38H72N2O11Color and Shape:White To Off-White SolidMolecular weight:733.00N-Nitroso-N-Desmethyl Tetracycline-d3 (N-Nitroso-N-Desmethyl Oxytetracycline EP Impurity B-d3)
Formula:C21H18D3N3O9Molecular weight:462.43Proguanil EP Impurity C HCl (Proguanil USP Related Compound C)
CAS:Formula:C14H13Cl2N5·HClMolecular weight:322.19 36.46N-Nitroso Tropicamide EP Impurity A (N-Nitroso Tropicamide USP Related Compound A)
CAS:Formula:C8H11N3OMolecular weight:165.20Latanoprost EP Impurity H-d4 (Latanoprost USP Related Compound E-d4)
CAS:Formula:C23H30D4O5Molecular weight:394.54Lynestrenol EP Impurity A
CAS:Formula:C20H28OColor and Shape:White To Off-White SolidMolecular weight:284.44Calcifediol EP Impurity A
CAS:Formula:C27H44O2Color and Shape:White To Off-White SolidMolecular weight:400.65Vinpocetine EP Impurity D (dihydrovinpocetine)
CAS:Formula:C22H28N2O2Color and Shape:White To Off-White SolidMolecular weight:352.48N-Nitroso-Tetracaine EP Impurity A (N-Nitroso-Benzylpenicillin (Procaine) EP Impurity A, N-Nitroso-4-Aminobenzoic Acid)
CAS:Formula:C7H6N2O3Molecular weight:166.14Simvastatin EP Impurity A (Simvastatin Acid, Tenivastatin)
CAS:Formula:C25H40O6Molecular weight:436.59Clozapine EP Impurity C HCl Salt
CAS:Formula:C17H17ClN4·HClColor and Shape:Yellow SolidMolecular weight:312.80 36.46C5-Nitroso Uridine (C5-Nitroso Adenosine EP Impurity F, C5-Nitroso Cytarabine EP Impurity B)
CAS:Formula:C9H11N3O7Molecular weight:273.20Methotrexate EP Impurity E-13C-d3 (Methotrexate USP Related Compound E-13C-d3)
Formula:C1413CH12D3N7O2Molecular weight:329.34Toladryl (Diphenhydramine EP Impurity B, Dimenhydrinate EP Impurity G, Orphenadrine EP Impurity F, Orphenadrine USP Related Compound F (Free Form))
CAS:Formula:C18H23NOMolecular weight:269.39Triflusal EP Impurity B-13C6 (Desacetyl Triflusalic Acid-13C6)
CAS:Formula:C213C6H5F3O3Molecular weight:212.07N-Nitroso Omeprazole EP Impurity C (N-Nitroso Omeprazole USP Related Compound C, N-Nitroso Esomeprazole EP Impurity C)
Formula:C17H18N4O3SMolecular weight:358.42Amitriptyline EP Impurity D (Nortriptyline EP Impurity D)
CAS:Formula:C20H25NOMolecular weight:295.43




