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

Cloprostenol Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cloprostenol API CS-T-13219 206555-98-8 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cloprostenol Sodium - Impurity A (Freebase) Impurity CS-T-95947 54276-22-1 Enquire
(5Z)-rel-Cloprostenol Sodium Impurity CS-T-13225 55028-72-3 Enquire
5,6-trans-Cloprostenol Impurity CS-DV-02989 57968-81-7 Enquire
d-Cloprostenol Sodium Salt Impurity CS-T-13226 62561-03-9 Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Cloprostenol Intermediate CS-K-00325 40665-92-7 Enquire


Chiral

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(+)-Cloprostenol Chiral CS-P-07444 1264-72-8 Enquire
(+)-Cloprostenol Isopropyl Ester Chiral CS-P-07445 157283-66-4 Enquire