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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Butamirate Citrate, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Butamirate Citrate 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 Butamirate Citrate-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.

Butamirate Citrate Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Butamirate Citrate API CS-T-49980 18109-81-4 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(E)-2-(2-(diethylamino)ethoxy)ethyl 2-phenylbut-2-enoate Impurity CS-O-38843 Not Available Enquire
Butamirate Citrate Impurity E Impurity CS-O-43174 Not Available Enquire