Amlodipine EP Impurity D Oxalate Salt

Product Name Amlodipine EP Impurity D Oxalate Salt
Alternate Names Amlodipine Impurities, Impurities of Amlodipine
CAT No. CS-O-07176
CAS No. 1216406-90-4
Category Impurities
Stock IN-Stock
Mol. Wt. 496.89 g/mol
Mol. For. C₂₂H₂₅ClN₂O₉
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Amlodipine
Purity 95%
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
Controlled No
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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.

Related Compounds

R-Amlodipine hemipentahydrate | Amlodipine EP Impurity E | Amlodipine Mannitol Adduct Acetate Salt | Amlodipine EP Impurity F | Amlodipine EP Impurity H | Amlodipine EP Impurity B | R-Amlodipine Besilate | Hydroxyethyl phthalyl amlodipine | Amlodipine Aspartic Acid Impurity | Amlodipine Impurity 61 | Amlodipine morpholine impurity | Amlodipine N-Galactose | Amlodipine EP Impurity C | Amlodipine Mannitol Adduct | Amlodipine Related Compound A | Di-acid Amlodipine | Amlodipine EP Impurity D HCl | N-Fomyl Amlodipine | Amlodipine Impurity F Maleate | Amlodipine EP Impurity A | Amlodipine EP Impurity G | Amlodipine Impurity 38 | N-Nitroso Amlodipine | Desmethyl Amlodipine | Deschloro Amlodipine | Amlodipine Besylate Impurity D Besylate salt | Amlodipine For Peak Identification | Amlodipine Impurity 32 | Amlodipine EP Impurity E Maleate | Amlodipine Impurity 34 | Amlodipine Azido Impurity | Amlodipine aminoethyl | Amlodipine Impurity 25 | Amlodipine Nitroso Impurity | Atorvastatin-Amlodipine Adduct | N-Nitroso Amlodipine EP Impurity F | Amlodipine Impurity | Amlodipine orotate | Amlodipine Impurity 8 | Atorvastatin Amlodipine Dimer | Phthaloyl Amlodipine Dimethyl Ester | Amlodipine N-Lactoside | Amlodipine Mannitol Adduct HCl Salt | Dimethoxy Impurity Deschloro Amlodipine | Amlodipine Galactose Adduct | Amlodipine Lactose adduct | Amlodipine Impurity 19 | Amlodipine Methyl Ester | Dehydro Amlodipine N-Oxide | Amlodipin EP Impurity D | Amlodipine Impurity 29 | Amlodipine Impurity 9 |

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