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

Esketamine Hydrochloride Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Esketamine Hydrochloride API CS-U-00151 33643-47-9 Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
1-Bromocyclopentyl 2-Chlorophenyl Ketone Intermediate CS-T-68407 6740-86-9 In Stock


Pharmaceutical Stds.

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(R)-Ketamine Pharmaceutical Stds. CS-TB-77699 33643-49-1 Enquire