Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors

Vemurafenib

Vemurafenib Impurities

Vemurafenib is a selective BRAF kinase inhibitor used in the treatment of metastatic melanoma with the BRAF V600E mutation. 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.

Vemurafenib EP Impurities

Pharmacopeial and non-pharmacopeial Vemurafenib 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.

Vemurafenib Related Compounds

Structurally related compounds and synthetic analogs associated with Vemurafenib 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.

Vemurafenib Impurity Reference Standards

Vemurafenib 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.

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 1714107-50-2

Mol F.

: C9H10BrN3O2

Mol W.

: 272.1

Cat No.

: SA96403

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 114042-02-3

Mol F.

: C6H5BrN2O2

Mol W.

: 217.0

Cat No.

: SA96402

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 3430-21-5

Mol F.

: C6H7BrN2

Mol W.

: 187.0

Cat No.

: SA96401

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 1186223-50-6

Mol F.

: C11H13F2NO4S

Mol W.

: 293.3

Cat No.

: SA96405

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 84832-01-9

Mol F.

: C8H5F2NO4

Mol W.

: 217.1

Cat No.

: SA96404

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 10147-36-1

Mol F.

: C3H7ClO2S

Mol W.

: 142.6

Cat No.

: SA96406

Please enquire for price & pack size
PLEASE ENQUIRE

CAS No.

: 918504-65-1

Mol F.

: C23H18ClF2N3O3S

Mol W.

: 489.9

Cat No.

: SA96400

Registration

Register to add the product to RFQ list

Already have an account?