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

Zuclopenthixol Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Zuclopenthixol-d4 (-)-10-Camphorsulfonic Acid Salt Stable Isotopes CS-T-99045 Not Available Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Zuclopenthixol decanoate API CS-O-05546 64053-00-5 Enquire
Zuclopenthixol diHydrochloride API CS-O-31171 58045-23-1 In Stock
Zuclopenthixol Hydrochloride API CS-EO-03951 1275595-34-0 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Zuclopenthixol Deconate Dihydrochloride Impurity CS-O-14594 1448876-93-4 In Stock
Zuclopenthixol acetate Impurity CS-O-02591 85721-05-7 Enquire