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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

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


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
O-(beta-Hydroxyethyl)rutoside Impurity CS-O-47030 23869-24-1 Enquire
Rutoside EP Impurity D Impurity CS-O-52304 2429978-69-6 Enquire
Rutoside EP Impurity E Impurity CS-O-58769 81970-00-5 Enquire
Rutoside EP Impurity F Impurity CS-O-52306 926664-29-1 Enquire
Rutoside Trihydrate EP Impurity E Impurity CS-O-52305 57528-70-8 Enquire
15,16-Di-O-acetyldarutoside Impurity CS-BT-00038 1188282-02-1 Enquire