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Brigatinib

Brigatinib Impurities

Brigatinib is a next-generation tyrosine kinase inhibitor (TKI) targeting ALK (anaplastic lymphoma kinase), used in the treatment of non-small cell lung cancer (NSCLC). Its impurity profile includes structurally related analogs, residual solvents, and degradation products formed under stress conditions such as hydrolysis, oxidation, and photolysis. Furthermore, typical degradation pathways involve oxidative modification of the heteroaromatic scaffold, hydrolytic cleavage of amide bonds, and rearrangement of substituents within the carbamate or urea moieties. These impurities may affect the drug’s potency, stability, and safety. Importantly, all impurities are structurally characterized and qualified according to ICH guidelines for toxicological assessment and analytical validation.

Brigatinib EP Impurities

Pharmacopeial and non-pharmacopeial Brigatinib impurity compounds are available in compliance with European Pharmacopoeia (EP) specifications. These standards support analytical method development, impurity profiling, and long-term stability studies. In addition, EP traceable materials are supplied with validated analytical data, including purity, structural confirmation, and spectral characterization.

Brigatinib Related Compounds

Structurally related compounds and synthetic analogs associated with Brigatinib are included for impurity identification, toxicological qualification, and regulatory submission. Consequently, these related substances are used in forced degradation studies, genotoxicity assessments, and impurity threshold evaluations. They are essential for understanding the impurity profile and ensuring compliance with regulatory limits.

Brigatinib Impurity Reference Standards

Brigatinib impurity reference standards are provided with validated analytical data, including purity, NMR, MS, and full Certificates of Analysis. These standards are used in pharmaceutical research, method validation, and GMP-compliant quality control. Additionally, EP/USP traceable entries are available upon request and are routinely re-tested to ensure consistency and reliability.

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CAS No.

: NA

Mol F.

: C29H38ClN8O3P

Mol W.

: 613.1

Cat No.

: SA96504

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CAS No.

: NA

Mol F.

: C29H37ClN9O4P

Mol W.

: 642.1

Cat No.

: SA96505

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CAS No.

: NA

Mol F.

: C29H38ClN8O3P

Mol W.

: 613.1

Cat No.

: SA96506

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CAS No.

: 1197961-02-6

Mol F.

: C30H41ClN7O2P

Mol W.

: 598.1

Cat No.

: SA96501

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CAS No.

: 1197953-54-0

Mol F.

: C29H39ClN7O2P

Mol W.

: 584.1

Cat No.

: SA96500

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CAS No.

: 1197958-75-0

Mol F.

: C28H37ClN7O2P

Mol W.

: 570.1

Cat No.

: SA96502

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CAS No.

: 1197960-18-1

Mol F.

: C30H41ClN7O2P

Mol W.

: 598.1

Cat No.

: SA96503

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