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Cilastatin Impurity 21

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For Research Use Only | Not For Clinical Use
CATAPB877674776
CAS877674-77-6
Structure
Synonyms(S,Z)-7-chloro-2-(2,2-dimethylcyclopropanecarboxamido)hept-2-enoic acid
Molecular Weight273.11
Molecular FormulaC13H20ClNO3

What is the product name of CAS 877674-77-6?

The product name is Cilastatin Impurity 21.

What is the molecular weight of Cilastatin Impurity 21?

The molecular weight is 273.11.

What is the molecular formula of Cilastatin Impurity 21?

The molecular formula is C13H20ClNO3.

What are the synonyms of Cilastatin Impurity 21?

One of the synonyms is (S,Z)-7-chloro-2-(2,2-dimethylcyclopropanecarboxamido)hept-2-enoic acid.

What is the chemical structure of Cilastatin Impurity 21?

The chemical structure is (S,Z)-7-chloro-2-(2,2-dimethylcyclopropanecarboxamido)hept-2-enoic acid.

Is Cilastatin Impurity 21 a pure compound?

No, it is an impurity of Cilastatin.

What is the significance of Cilastatin Impurity 21 in pharmaceutical manufacturing?

It is important to control and monitor impurities such as Cilastatin Impurity 21 in pharmaceutical manufacturing to ensure product quality and safety.

How is Cilastatin Impurity 21 typically detected and quantified in pharmaceutical products?

Analytical techniques such as HPLC (High Performance Liquid Chromatography) are commonly used to detect and quantify impurities like Cilastatin Impurity 21.

What potential impact can impurities like Cilastatin Impurity 21 have on the efficacy of pharmaceutical products?

Impurities can affect the potency, stability, and safety of pharmaceutical products, so it is important to monitor and control them during manufacturing.

Are there regulatory guidelines and limits for impurities like Cilastatin Impurity 21 in pharmaceutical products?

Yes, regulatory agencies such as the FDA and EMA have set limits on impurities in pharmaceutical products to ensure patient safety and product quality.

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