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Amlodipine EP Impurity D Oxalate Salt

Chemical Name Amlodipine EP Impurity D Oxalate Salt
CAT No. CS-O-07176
CAS No. 1216406-90-4
Status Available for Immediate Dispatch
Category Impurities
Mol. Wt. 496.89 mol/g
Mol. For. C₂₂H₂₅ClN₂O₉
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information


Packing Product will be supplied in Vials, in certain conditions we also use 'Septa Vials'
Controlled No
Parent API Amlodipine
Purity Not less than 90%
Therapeutic Anti-Hypertensives
Smileys CCOC(=O)C1=C(C(=C(N=C1COCCN)C)C(=O)OC)C2=CC=CC=C2Cl.C(=O)(C(=O)O)O
Canonical Smiles CCOC(=O)C1=C(C(=C(N=C1COCCN)C)C(=O)OC)C2=CC=CC=C2Cl.C(=O)(C(=O)O)O
InchIKey VAHKAMHZXZAAGV-UHFFFAOYSA-N
Inchl InChI=1S/C20H23ClN2O5.C2H2O4/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21;3-1(4)2(5)6/h5-8H,4,9-11,22H2,1-3H3;(H,3,4)(H,5,6)
IUPAC 3-O-ethyl 5-O-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate;oxalic acid
Hazardous Yes


Usage and description


Amlodipine EP Impurity D Oxalate Salt is a chemical compound that is commonly used in the pharmaceutical industry. It is a derivative of the drug Amlodipine, which is a calcium channel blocker that is used to treat hypertension and angina. This impurity is produced during the synthesis of Amlodipine and is considered to be an unwanted byproduct that needs to be removed from the final product. The chemical formula of Amlodipine EP Impurity D Oxalate Salt is C20H25ClN2O8, and it has a molecular weight of 456.88 g/mol. This compound is a white to off-white crystalline powder that is soluble in water and ethanol. It is also stable under normal conditions of storage and handling. Although Amlodipine EP Impurity D Oxalate Salt is not used as a drug itself, it is important to monitor its presence in Amlodipine samples. This is because the impurity can affect the purity and potency of the final drug product. As such, regulatory agencies such as the US Food and Drug Administration (FDA) have set limits on the amount of impurities that are allowed in drug products. In summary, Amlodipine EP Impurity D Oxalate Salt is an unwanted impurity that is produced during the synthesis of Amlodipine. It needs to be monitored and controlled to ensure the purity and potency of the final drug product.

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