Captopril EP Impurity M

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For Research Use Only | Not For Clinical Use

CAT	APB83326981
CAS	83326-98-1
Molecular Weight	335.43
Molecular Formula	C13H21NO5S2

What is the product name of the compound with CAS number 83326-98-1?

The product name is Captopril EP Impurity M.

What is the molecular weight of Captopril EP Impurity M?

The molecular weight is 335.43.

What is the molecular formula of Captopril EP Impurity M?

The molecular formula is C13H21NO5S2.

Is Captopril EP Impurity M a common impurity found in captopril?

Yes, Captopril EP Impurity M is an impurity commonly found in captopril.

What is the significance of knowing the impurities present in captopril?

Knowing the impurities present in captopril is important for quality control and ensuring safety of the drug.

How can Captopril EP Impurity M be identified and quantified in captopril samples?

Captopril EP Impurity M can be identified and quantified using analytical techniques such as chromatography.

What are some potential health risks associated with the presence of impurities in pharmaceuticals?

Impurities in pharmaceuticals can potentially cause adverse effects on patients' health and reduce the effectiveness of the drug.

Are there regulations in place to lim- It the amount of impurities allowed in pharmaceutical products?

Yes, regulatory bodies set limits on the amount of impurities allowed in pharmaceutical products to ensure safety and quality.

How can manufacturers ensure that their pharmaceutical products meet regulatory requirements for impurity levels?

Manufacturers can conduct thorough quality control testing to assess impurity levels and ensure compliance with regulatory standards.

What steps can be taken to minimize the presence of impurities in the production of pharmaceuticals?

Proper quality control measures, careful handling of raw materials, and adherence to good manufacturing practices can help minimize the presence of impurities in pharmaceutical production.

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