Simvastatin EP Impurity A

Product Name Simvastatin EP Impurity A
Alternate Names Simvastatin Impurities, Impurities of Simvastatin
CAT No. CS-O-08179
CAS No. 101314-97-0
Category Impurities
Stock IN-Stock
Mol. Wt. 458.56 g/mol
Mol. For. C25H39O6 : Na
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Simvastatin
Purity 95%
Therapeutic Anti-Diabetic
Smileys O=C(C(C)(C)CC)O[C@@H]1[C@@]([C@H]2CC[C@@H](O)C[C@@H](O)CC(O)=O)([H])C(C=C[C@@H]2C)=C[C@H](C)C1.[NaH]
Canonical Smiles CCC(C)(C)C(=O)OC1CC(C=C2C1C(C(C=C2)C)CCC(CC(CC(=O)[O-])O)O)C.[Na+]
InchIKey RLWRROYWKHUVKF-OKDJMAGBSA-M
Inchl InChI=1S/C25H40O6.Na/c1-6-25(4,5)24(30)31-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-18(26)13-19(27)14-22(28)29;/h7-8,11,15-16,18-21,23,26-27H,6,9-10,12-14H2,1-5H3,(H,28,29);/q;+1/p-1/t15-,16-,18+,19+,20-,21-,23-;/m0./s1
IUPAC sodium;(3R,5R)-7-[(1S,2S,6R,8S,8aR)-8-(2,2-dimethylbutanoyloxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate
Controlled No
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Simvastatin EP Impurity A is a chemical compound that is used in the pharmaceutical industry as a reference standard during the quality control of Simvastatin, a commonly prescribed medication for lowering cholesterol levels in the bloodstream. Simvastatin EP Impurity A is a by-product of the synthesis of Simvastatin, and its presence in Simvastatin preparations can affect the stability and efficacy of the medication. Therefore, it is important to monitor the levels of Simvastatin EP Impurity A in Simvastatin formulations to ensure their safety and effectiveness. The chemical formula of Simvastatin EP Impurity A is C25H38O5, and its molecular weight is 418.57 g/mol. It is a white to off-white powder that is sparingly soluble in water and soluble in organic solvents such as methanol and ethanol. The chemical structure of Simvastatin EP Impurity A is similar to that of Simvastatin, with the exception of an additional hydroxyl group at position 3 of the butyrolactone ring. This structural difference can affect the pharmacological properties of Simvastatin EP Impurity A and its interaction with other compounds. In conclusion, Simvastatin EP Impurity A is an important reference standard for the quality control of Simvastatin preparations. Its chemical properties and structure play a crucial role in the stability and efficacy of Simvastatin, and its careful monitoring is essential for ensuring the safety and effectiveness of Simvastatin-based medications.

Related Compounds

Simvastatin 6-Oxo Isomer | Simvastatin (6R)-Hydroxy Isomer | Simvastatin Acid Ethyl Ester | Simvastatin EP Impurity G | Simvastatin (3S)-Hydroxy Impurity | Simvastatin, 1-Pyreneacetyl Ester | Simvastatin EP Impurity C | Simvastatin (6S)-Hydroxy Isomer | Simvastatin 4'-Methyl Ether | Simvastatin Acid Glycerol Ester | Simvastatin EP Impurity K | Simvastatin EP Impurity B | Simvastatin pivaloyl Dehydro impurity | Simvastatin Impurity K | Simvastatin Anhydro Acid Sodium Salt | Simvastatin EP Impurity E | Simvastatin pivaloyl impurity | Simvastatin EP Impurity D | Simvastatin Acid Methyl Ester | Simvastatin (3R)-Hydroxy Impurity |

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