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Ceritinib Impurity 1

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For Research Use Only | Not For Clinical Use
CATAPB04678
Synonyms1-chloro-5-isopropoxy-2-methyl-3-nitrobenzene
Molecular Weight229.66
Molecular FormulaC10H12ClNO3

What is the molecular weight of Ceritinib Impurity 1?

The molecular weight of Ceritinib Impurity 1 is 229.66.

What is the molecular formula of Ceritinib Impurity 1?

The molecular formula of Ceritinib Impurity 1 is C10H12ClNO3.

What are some synonyms for Ceritinib Impurity 1?

One synonym for Ceritinib Impurity 1 is 1-chloro-5-isopropoxy-2-methyl-3-nitrobenzene.

What are the key structural features of Ceritinib Impurity 1?

The key structural features of Ceritinib Impurity 1 include a chlorine atom, an isopropoxy group, a methyl group, and a nitro group on a benzene ring.

How many carbon atoms are present in Ceritinib Impurity 1?

Ceritinib Impurity 1 contains 10 carbon atoms.

What is the role of Ceritinib Impurity 1 in pharmaceuticals?

Ceritinib Impurity 1 is a chemical compound that may be used in the pharmaceutical industry as an impurity or precursor in the production of ceritinib.

How is Ceritinib Impurity 1 synthesized?

Ceritinib Impurity 1 can be synthesized through chemical reactions involving chlorination, alkylation, and nitration of benzene derivatives.

Why is it important to identify and characterize Ceritinib Impurity 1 in pharmaceutical formulations?

Identifying and characterizing Ceritinib Impurity 1 in pharmaceutical formulations is important to ensure the quality, safety, and efficacy of the drug product.

What analytical methods can be used to detect Ceritinib Impurity 1?

Analytical methods such as high-performance liquid chromatography (HPLC) and mass spectrometry can be used to detect Ceritinib Impurity 1 in samples.

How can the presence of Ceritinib Impurity 1 impact the stability of a pharmaceutical product?

The presence of Ceritinib Impurity 1 can impact the stability of a pharmaceutical product by potentially affecting its shelf life, potency, and overall quality.

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