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Cilastatin EP Impurity E

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For Research Use Only | Not For Clinical Use
CATAPB1174657078
CAS1174657-07-8
Synonyms(R)-7-((2-amino-2-carboxyethyl)thio)-2-oxoheptanoic acid
Molecular Weight263.31
Molecular FormulaC10H17NO5S

What is the specific name of this impurity?

The specific name of this impurity is Cilastatin EP Impurity E.

What is the CAS number for Cilastatin EP Impurity E?

The CAS number for Cilastatin EP Impurity E is 1174657-07-8.

What are the synonyms for Cilastatin EP Impurity E?

One of the synonyms for Cilastatin EP Impurity E is (R)-7-((2-amino-2-carboxyethyl)thio)-2-oxoheptanoic acid.

What is the molecular weight of Cilastatin EP Impurity E?

The molecular weight of Cilastatin EP Impurity E is 263.31.

What is the molecular formula of Cilastatin EP Impurity E?

The molecular formula of Cilastatin EP Impurity E is C10H17NO5S.

How does Cilastatin EP Impurity E differ from the main compound Cilastatin?

Cilastatin EP Impurity E is an impurity of Cilastatin and differs in its chemical structure.

Is Cilastatin EP Impurity E a common impurity found in products containing Cilastatin?

Cilastatin EP Impurity E may be a common impurity found in products containing Cilastatin, but Further testing may be necessary to confirm this.

Can Cilastatin EP Impurity E impact the effectiveness or safety of products containing Cilastatin?

Impurities like Cilastatin EP Impurity E can potentially impact the effectiveness or safety of products containing Cilastatin, which is why it is important to monitor and control impurity levels.

Are there regulatory guidelines for the acceptable levels of Cilastatin EP Impurity E in pharmaceutical products?

Regulatory guidelines may exist for the acceptable levels of impurities like Cilastatin EP Impurity E in pharmaceutical products to ensure they meet safety and quality standards.

How is Cilastatin EP Impurity E typically identified and quantified in pharmaceutical products?

Cilastatin EP Impurity E can be identified and quantified through analytical testing methods such as chromatography to ensure product quality and compliance with regulatory standards.

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