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

Indoramin Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Indoramin-d5 Stable Isotopes CS-O-06681 57165-41-0 In Stock


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Indoramine API Standards CS-P-01047 26844-12-2 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
6-Hydroxyindoramin Hydrochloride Impurities CS-T-56098 79146-88-6 Enquire


Intermediates

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Indoramin Hydrochloride Intermediates CS-T-29338 38821-52-2 Enquire