Simvastatin EP Impurity D

Product Name Simvastatin EP Impurity D
Alternate Names Simvastatin Impurities, Impurities of Simvastatin
CAT No. CS-O-08182
CAS No. 476305-24-5
Category Impurities
Stock IN-Stock
Mol. Wt. 837.13 g/mol
Mol. For. C₅₀H₇₆O₁₀
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Simvastatin
Purity 95%
Therapeutic Anti-Diabetic
Smileys C[C@@H](C=C1)[C@@H]([C@]2([H])C1=C[C@H](C)C[C@@H]2OC(C(C)(C)CC)=O)CC[C@@H](OC3=O)C[C@H](C3)OC(C[C@H](O)C[C@H](O)CC[C@@H]([C@H](C=C4)C)[C@]5([H])C4=C[C@H](C)C[C@@H]5OC(C(C)(C)CC)=O)=O
Canonical Smiles CCC(C)(C)C(=O)OC1CC(C=C2C1C(C(C=C2)C)CCC3CC(CC(=O)O3)OC(=O)CC(CC(CCC4C(C=CC5=CC(CC(C45)OC(=O)C(C)(C)CC)C)C)O)O)C
InchIKey GUEULYYYHDURDF-CWZAOXTASA-N
Inchl InChI=1S/C50H76O10/c1-11-49(7,8)47(55)59-41-23-29(3)21-33-15-13-31(5)39(45(33)41)19-17-35(51)25-36(52)26-43(53)58-38-27-37(57-44(54)28-38)18-20-40-32(6)14-16-34-22-30(4)24-42(46(34)40)60-48(56)50(9,10)12-2/h13-16,21-22,29-32,35-42,45-46,51-52H,11-12,17-20,23-28H2,1-10H3/t29-,30-,31-,32-,35+,36+,37+,38+,39-,40-,41-,42-,45-,46-/m0/s1
IUPAC [(2R,4R)-2-[2-[(1S,2S,6R,8S,8aR)-8-(2,2-dimethylbutanoyloxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-6-oxooxan-4-yl] (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 D is a chemical compound that is commonly used in the pharmaceutical industry. It is a known impurity of Simvastatin, which is a medication used for the treatment of high cholesterol levels in the blood. Simvastatin EP Impurity D is usually found in trace amounts in Simvastatin products, and it is important to monitor its levels as it can affect the efficacy of the medication. The chemical formula of Simvastatin EP Impurity D is C25H42O3, and its molecular weight is 390.6 g/mol. It is a white crystalline solid that is soluble in organic solvents such as methanol and ethanol. Simvastatin EP Impurity D is typically synthesized using chemical methods, and its purity is determined using various analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). In terms of usage, Simvastatin EP Impurity D is mainly used as a reference standard in quality control laboratories for the analysis of Simvastatin products. It is also used in research studies to investigate the metabolism and pharmacokinetics of Simvastatin in the body. The presence of Simvastatin EP Impurity D in Simvastatin products can affect the potency and efficacy of the medication, and therefore it is important to monitor its levels to ensure patient safety and efficacy.

Related Compounds

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

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