Cilastatin EP Impurity F

Product Name Cilastatin EP Impurity F
Alternate Names Cilastatin Impurities, Impurities of Cilastatin
CAT No. CS-EO-00161
CAS No. Not Available
Category Impurities
Stock IN-Stock
Mol. Wt. 358.45 g/mol
Mol. For. C₁₆H₂₆N₂O₅S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Cilastatin
Purity 95%
Smileys O=C(O)/C(NC(C(C)C(C)=C)=O)=C/CCCCSC[C@H](N)C(O)=O
Controlled No
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Cilastatin EP Impurity F, also known as 7-(S)-[(4-chlorophenyl)sulfonyl]-6-hydroxy-2,3-dihydro-1H-indene-1-carboxylic acid, is an organic compound that is commonly used as an impurity standard in the pharmaceutical industry. This impurity is typically found in small quantities in cilastatin, a medication used to prevent the breakdown of the antibiotic drug imipenem. Cilastatin EP Impurity F is primarily used as a reference standard in the development and validation of analytical methods for the detection and quantification of cilastatin and its related impurities. It is also used as a quality control standard in the production of cilastatin and related drugs. In terms of its chemical properties, Cilastatin EP Impurity F is a white to off-white powder that is sparingly soluble in water and soluble in organic solvents such as methanol and acetonitrile. Its molecular formula is C16H13ClO4S and it has a molecular weight of 346.79 g/mol. Overall, Cilastatin EP Impurity F plays an important role in ensuring the quality and safety of cilastatin and related drugs, making it a valuable tool in the pharmaceutical industry.

Related Compounds

Cilastatin EP Impurity G | Cilastatin EP Impurity A | Cilastatin EP Impurity E | Cilastatin EP Impurity H | Cilastatin EP Impurity C | Cilastatin EP Impurity B | Cilastatin Ammonium Salt USP |

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