Agomelatine impurity 13

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CAT	APB139525772
CAS	139525-77-2
Structure
Synonyms	2-(7-methoxynaphthalen-1-yl)ethan-1-aminehydrochloride
Molecular Weight	201.26
Molecular Formula	C13H15NO

What is the product name for CAS 139525-77-2?

The product name is Agomelatine impurity 13.

What are some synonyms for Agomelatine impurity 13?

One synonym for Agomelatine impurity 13 is 2-(7-methoxynaphthalen-1-yl)ethan-1-aminehydrochloride.

What is the molecular weight of Agomelatine impurity 13?

The molecular weight of Agomelatine impurity 13 is 201.26.

What is the molecular formula of Agomelatine impurity 13?

The molecular formula of Agomelatine impurity 13 is C13H15NO.

What is the chemical structure of Agomelatine impurity 13?

The chemical structure of Agomelatine impurity 13 consists of a 7-methoxynaphthalen-1-yl group attached to an ethan-1-amine.

Why is Agomelatine impurity 13 classified as an impurity?

Agomelatine impurity 13 is classified as an impurity because it is a byproduct or contaminant that may be present in the synthesis or production of agomelatine.

What role does the hydrochloride group play in the chemical composition of Agomelatine impurity 13?

The hydrochloride group in Agomelatine impurity 13 likely contributes to its solubility and stability in certain solvents.

How is Agomelatine impurity 13 typically identified in laboratory settings?

Agomelatine impurity 13 can be identified using analytical techniques such as HPLC (High-Performance Liquid Chromatography) or NMR (Nuclear Magnetic Resonance) spectroscopy.

What potential impact could the presence of Agomelatine impurity 13 have on the effectiveness or safety of agomelatine as a drug?

The presence of impurities like Agomelatine impurity 13 in agomelatine could affect its purity, potency, or stability, potentially impacting its effectiveness or safety as a medication.

Are there regulations or guidelines in place regarding the acceptable levels of impurities in pharmaceutical products like agomelatine?

Yes, regulatory agencies such as the FDA (Food and Drug Administration) have strict guidelines and limits for impurities in pharmaceutical products to ensure their quality, safety, and effectiveness.

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