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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Tivozanib, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Tivozanib impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Tivozanib-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Tivozanib Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Tivozanib 13CD3 Stable Isotopes CS-O-44732 Not Available Enquire
Tivozanib-D6 Stable Isotopes CS-O-48182 1714998-87-4 Enquire
Tivozanib 13C4, 15N Stable Isotopes CS-EK-02640 475108-18-0 (unlabelled) Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Tivozanib hydrochloride hydrate API CS-O-44981 682745-41-1 Enquire
Tivozanib API CS-T-44458 475108-18-0 Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
4-Chloro-6-methoxyquinolin-7-ol Intermediate CS-M-57904 205448-31-3 Enquire


Nitrosamine

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
N-Nitroso Tivozanib impurity E Nitrosamine CS-O-56025 ---- Enquire