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Rosuvastatin Impurity 195

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For Research Use Only | Not For Clinical Use
CATAPB01774
Synonyms2-((4R,6S)-2,2-dimethyl-6-(((5-methyl-1,3,4-thiadiazol-2-yl)sulfonyl)methyl)-1,3-dioxan-4-yl)acetic acid
Molecular Weight350.41
Molecular FormulaC12H18N2O6S2

What is the molecular weight of Rosuvastatin Impurity 195?

The molecular weight of Rosuvastatin Impurity 195 is 350.41.

What is the molecular formula of Rosuvastatin Impurity 195?

The molecular formula of Rosuvastatin Impurity 195 is C12H18N2O6S2.

What are some synonyms for Rosuvastatin Impurity 195?

One of the synonyms is 2-((4R,6S)-2,2-dimethyl-6-(((5-methyl-1,3,4-thiadiazol-2-yl)sulfonyl)methyl)-1,3-dioxan-4-yl)acetic acid.

What is the chemical structure of Rosuvastatin Impurity 195?

The chemical structure of Rosuvastatin Impurity 195 consists of a dioxane ring with a thiadiazole sulfone substituent.

What is the stereochemistry of Rosuvastatin Impurity 195?

Rosuvastatin Impurity 195 has a stereochemistry of (4R,6S) based on its chemical structure.

How many sulfur atoms are present in the molecular formula of Rosuvastatin Impurity 195?

There are two sulfur atoms present in the molecular formula of Rosuvastatin Impurity 195.

What is the role of Rosuvastatin Impurity 195 in pharmaceutical manufacturing?

Rosuvastatin Impurity 195 is considered an impurity that needs to be monitored and controlled in pharmaceutical manufacturing processes.

What potential impact can Rosuvastatin Impurity 195 have on the purity and stability of rosuvastatin drug products?

The presence of Rosuvastatin Impurity 195 can affect the purity and stability of rosuvastatin drug products, potentially leading to decreased efficacy or safety concerns.

How is Rosuvastatin Impurity 195 typically detected and quantified in pharmaceutical samples?

Rosuvastatin Impurity 195 is typically detected and quantified using analytical techniques such as HPLC (High-Performance Liquid Chromatography).

What steps can be taken to minimize the presence of Rosuvastatin Impurity 195 in pharmaceutical products?

To minimize the presence of Rosuvastatin Impurity 195, manufacturers can implement strict quality control measures, optimize synthesis processes, and conduct thorough impurity profiling studies.

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