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

Lafutidine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Lafutidine-D10 Stable Isotopes CS-P-01083 118288-08-7 (Unlabelled) Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Lafutidine API Standards CS-O-01780 118288-08-7 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Dihydro Lafutidine Impurities CS-T-18790 118288-14-5 Enquire
Lafutidine Impurity B Impurities CS-T-30813 174583-84-7 Enquire
rac Lafutidine Impurities CS-T-30808 206449-93-6 Enquire
rac trans-Lafutidine Impurities CS-T-30810 206449-94-7 Enquire