Bictegravir Impurity 13

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For Research Use Only | Not For Clinical Use

CAT	APB03694
Synonyms	1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylic acid
Molecular Weight	301.251
Molecular Formula	C12H15NO8

What is the product name of Bictegravir Impurity 13?

The product name of Bictegravir Impurity 13 is Bictegravir Impurity 13.

What are the synonyms of Bictegravir Impurity 13?

One of the synonyms is 1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylic acid.

What is the molecular weight of Bictegravir Impurity 13?

The molecular weight of Bictegravir Impurity 13 is 301.251.

What is the molecular formula of Bictegravir Impurity 13?

The molecular formula of Bictegravir Impurity 13 is C12H15NO8.

What is the chemical structure of Bictegravir Impurity 13?

The chemical structure of Bictegravir Impurity 13 is 1-(2,2-dimethoxyethyl)-3-methoxy-4-oxo-1,4-dihydropyridine-2,5-dicarboxylic acid.

What is the chemical composition of Bictegravir Impurity 13?

The chemical composition of Bictegravir Impurity 13 includes carbon, hydrogen, nitrogen, and oxygen atoms.

Why is Bictegravir Impurity 13 considered an impurity?

Bictegravir Impurity 13 is considered an impurity because it is a byproduct or degradation product formed during the synthesis or storage of the main compound, Bictegravir.

How can Bictegravir Impurity 13 impact the quality of pharmaceutical products?

Bictegravir Impurity 13 can impact the quality of pharmaceutical products by potentially affecting the efficacy, safety, and stability of the final drug formulation.

What are some methods used to detect and quantify Bictegravir Impurity 13?

Methods such as chromatography (e.g., HPLC) and spectroscopy (e.g., UV-Vis) can be used to detect and quantify Bictegravir Impurity 13 in pharmaceutical samples.

How can the presence of Bictegravir Impurity 13 be controlled in pharmaceutical manufacturing processes?

The presence of Bictegravir Impurity 13 can be controlled in pharmaceutical manufacturing processes by optimizing reaction conditions, purification steps, and storage conditions to minimize impurity formation.

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