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

Rutoside Related Compounds

API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Rutoside Trihydrate API Standards CS-O-05209 250249-75-3 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
"15,16-Di-O-acetyldarutoside" Impurities CS-BT-00038 1188282-02-1 Enquire
O-(beta-Hydroxyethyl)rutoside Impurities CS-O-47030 23869-24-1 Enquire
Rutoside Trihydrate EP Impurity E Impurities CS-O-52305 57528-70-8 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
3’,4’-Bis(hydroxyethyl)rutoside Intermediates CS-T-66985 862127-01-3 Enquire