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

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

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