Albuterol Impurity 39

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For Research Use Only | Not For Clinical Use

CAT	APB03077
Synonyms	2-(tert-butylamino)-1-(4-hydroxyphenyl)ethanone
Molecular Weight	207.13
Molecular Formula	C12H17NO2

What is the molecular weight of Albuterol Impurity 39?

The molecular weight of Albuterol Impurity 39 is 207.13.

What is the molecular formula of Albuterol Impurity 39?

The molecular formula of Albuterol Impurity 39 is C12H17NO2.

What are the synonyms for Albuterol Impurity 39?

One of the synonyms is 2-(tert-butylamino)-1-(4-hydroxyphenyl)ethanone.

How many carbon atoms are present in the molecular formula of Albuterol Impurity 39?

There are 12 carbon atoms present in the molecular formula of Albuterol Impurity 39.

What functional groups are present in Albuterol Impurity 39?

The functional groups present in Albuterol Impurity 39 include an amine group, a phenol group, and a ketone group.

What is the significance of Impurity 39 in the context of Albuterol?

Impurity 39 is a specific chemical entity that may be present alongside Albuterol, potentially affecting its purity and quality.

How is Albuterol Impurity 39 typically synthesized?

Albuterol Impurity 39 is typically synthesized through chemical reactions involving tert-butylamine, 4-hydroxyphenylacetic acid, and reagents for ketone formation.

What is the role of Albuterol Impurity 39 in pharmaceutical formulations?

In pharmaceutical formulations, Albuterol Impurity 39 may be considered an unwanted byproduct that needs to be monitored and controlled for safety and efficacy.

Why is it important to identify and quantify Albuterol Impurity 39 in pharmaceutical products?

Identifying and quantifying Albuterol Impurity 39 is important for regulatory compliance, ensuring product quality, and evaluating potential health risks associated with impurities.

How can analytical techniques such as HPLC or mass spectrometry be used to detect Albuterol Impurity 39?

Analytical techniques such as HPLC (High Performance Liquid Chromatography) or mass spectrometry can be used to separate, detect, and quantify Albuterol Impurity 39 in pharmaceutical samples.

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