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

Acrivastine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Acrivastine-d7 Stable Isotopes CS-CX-00054 172165-56-9 In Stock
Acrivastine-d8 Stable Isotopes CS-T-101943 Not Available Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Acrivastine API Standards CS-O-00802 87848-99-5 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Acrivastine isomer Z Impurities CS-CX-00053 1057138-89-2 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
2,3-Dihydro Acrivastine Intermediates CS-T-88315 87849-01-2 Enquire