Rosuvastatin Impurity 112

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For Research Use Only | Not For Clinical Use

CAT	APB404958083
CAS	404958-08-3
Structure
Molecular Weight	236.69
Molecular Formula	C10H17ClO4

What is the product name of CAS 404958-08-3?

The product name is Rosuvastatin Impurity 112.

What is the molecular weight of Rosuvastatin Impurity 112?

The molecular weight is 236.69.

What is the molecular formula of Rosuvastatin Impurity 112?

The molecular formula is C10H17ClO4.

What is the chemical structure of Rosuvastatin Impurity 112?

The chemical structure of Rosuvastatin Impurity 112 is comprised of 10 carbon atoms, 17 hydrogen atoms, one chlorine atom, and four oxygen atoms.

What is the significance of identifying impurities in a drug like Rosuvastatin?

Identifying impurities in drugs like Rosuvastatin is crucial for ensuring the safety and efficacy of the final product for patient use.

How is Rosuvastatin Impurity 112 different from the main active ingredient, Rosuvastatin?

Rosuvastatin Impurity 112 is an impurity of Rosuvastatin, which means it is present in the drug as a byproduct or contaminant, whereas Rosuvastatin is the main active ingredient with therapeutic effects.

How is Rosuvastatin Impurity 112 produced in the manufacturing process of Rosuvastatin?

Rosuvastatin Impurity 112 may be produced as a result of certain steps in the manufacturing process of Rosuvastatin, such as chemical reactions or degradation of the main compound.

What are the potential risks associated with the presence of impurities like Rosuvastatin Impurity 112 in a drug product?

Impurities in drug products can pose risks such as reduced potency, decreased stability, potential toxicity, and adverse effects on patients.

How is Rosuvastatin Impurity 112 identified and quantified during the quality control of Rosuvastatin products?

Rosuvastatin Impurity 112 can be identified and quantified through various analytical techniques such as chromatography, spectroscopy, and mass spectrometry as part of quality control processes.

What are the regulatory guidelines for permissible levels of impurities in pharmaceutical products like Rosuvastatin?

Regulatory authorities set limits for allowable levels of impurities in pharmaceutical products, and manufacturers must adhere to these guidelines to ensure product quality and patient safety.

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