Rosuvastatin Impurity 130

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For Research Use Only | Not For Clinical Use

CAT	APB01663
Synonyms	(3R,5S)-6-(benzo[d]thiazol-2-ylsulfonyl)-3,5-dihydroxyhexanoic acid
Molecular Weight	345.39
Molecular Formula	C13H15NO6S2

What is the product name of Rosuvastatin Impurity 130?

The product name of Rosuvastatin Impurity 130 is Rosuvastatin Impurity 130.

What are the synonyms for Rosuvastatin Impurity 130?

One of the synonyms for Rosuvastatin Impurity 130 is (3R,5S)-6-(benzo[d]thiazol-2-ylsulfonyl)-3,5-dihydroxyhexanoic acid.

What is the molecular weight of Rosuvastatin Impurity 130?

The molecular weight of Rosuvastatin Impurity 130 is 345.39.

What is the molecular formula of Rosuvastatin Impurity 130?

The molecular formula of Rosuvastatin Impurity 130 is C13H15NO6S2.

How many oxygen atoms are present in the molecular formula of Rosuvastatin Impurity 130?

There are six oxygen atoms present in the molecular formula of Rosuvastatin Impurity 130.

What is the chemical structure of Rosuvastatin Impurity 130?

The chemical structure of Rosuvastatin Impurity 130 includes a sulfur atom, a nitrogen atom, and a benzothiazole moiety.

What is the role of Rosuvastatin Impurity 130 in pharmaceutical development?

Rosuvastatin Impurity 130 is a known pharmaceutical impurity that must be carefully monitored and controlled during the development of Rosuvastatin drugs.

How does Rosuvastatin Impurity 130 affect the purity and efficacy of Rosuvastatin drugs?

If not removed or reduced to acceptable levels, Rosuvastatin Impurity 130 can impact the overall purity and efficacy of Rosuvastatin drugs, potentially leading to negative health effects.

How is Rosuvastatin Impurity 130 typically identified and quantified in pharmaceutical formulations?

Rosuvastatin Impurity 130 is typically identified and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and mass spectrometry.

What precautions should be taken in the manufacturing and quality control of Rosuvastatin drugs to ensure the control of Rosuvastatin Impurity 130?

Manufacturers and quality control personnel should implement strict protocols, analytical methods, and monitoring processes to ensure the control and reduction of Rosuvastatin Impurity 130 in Rosuvastatin drug formulations.

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