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Amlodipine Impurity 17

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For Research Use Only | Not For Clinical Use
CATAPB19532979
CAS19532-97-9
SynonymsN1,N2-bis(2-hydroxyethyl)phthalamide
Molecular Weight252.27
Molecular FormulaC12H16N2O4

What is the product name of Amlodipine Impurity 17?

The product name of Amlodipine Impurity 17 is N1,N2-bis(2-hydroxyethyl)phthalamide.

What is the CAS number for Amlodipine Impurity 17?

The CAS number for Amlodipine Impurity 17 is 19532-97-9.

What is the molecular weight of Amlodipine Impurity 17?

The molecular weight of Amlodipine Impurity 17 is 252.27.

What is the molecular formula of Amlodipine Impurity 17?

The molecular formula of Amlodipine Impurity 17 is C12H16N2O4.

What are the synonyms for Amlodipine Impurity 17?

One synonym for Amlodipine Impurity 17 is N1,N2-bis(2-hydroxyethyl)phthalamide.

What are the chemical elements present in the molecular formula of Amlodipine Impurity 17?

The chemical elements present in the molecular formula of Amlodipine Impurity 17 are carbon, hydrogen, nitrogen, and oxygen.

What is the purpose of identifying impurities in a pharmaceutical product such as Amlodipine Impurity 17?

Identifying impurities in a pharmaceutical product like Amlodipine Impurity 17 is important for ensuring the safety, efficacy, and quality of the product.

How is Amlodipine Impurity 17 typically characterized and quantified in pharmaceutical research and development?

Amlodipine Impurity 17 is typically characterized and quantified using analytical techniques such as chromatography and spectroscopy in pharmaceutical research and development.

What are some potential sources of Amlodipine Impurity 17 in the manufacturing process of pharmaceutical products?

Potential sources of Amlodipine Impurity 17 in the manufacturing process of pharmaceutical products include impurities in raw materials, degradation of the active ingredient, and chemical reactions during synthesis.

How can the presence of Amlodipine Impurity 17 impact the safety and efficacy of pharmaceutical products containing amlodipine?

The presence of Amlodipine Impurity 17 can impact the safety and efficacy of pharmaceutical products containing amlodipine by potentially causing adverse reactions or reducing the therapeutic effectiveness of the medication.

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