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

Tofisopam Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Tofisopam API CS-O-30804 22345-47-7 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3-(2-(3,4-Dimethoxybenzoyl)-4,5-Dimethoxyphenyl)Pentan-2-One Impurity CS-MM-09226 15462-91-6 In Stock
Tofisopam Impurity 1 Impurity CS-EO-03119 37952-09-3 Enquire
Tofisopam Impurity 3 Impurity CS-EO-03118 6379-72-2 Enquire
Tofisopam impurity C Impurity CS-O-32558 4483-47-0 In Stock


Fine Chemicals

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(-)-Tofisopam Fine Chemicals CS-O-37513 82059-51-6 Enquire