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

Enalaprilat Dihydrate Related Compounds

API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Enalaprilat Dihydrate API CS-T-21619 84680-54-6 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Enalaprilat EP Impurity G Impurity CS-EO-00956 284677-66-3 In Stock
Enalaprilat EP Impurity A Impurity CS-EO-00951 112318-07-7 Enquire
Enalaprilat EP Impurity B Impurity CS-EO-00952 Not Available Enquire
Enalaprilat EP Impurity C Impurity CS-EO-00953 Not Available Enquire
Enalaprilat EP Impurity D Impurity CS-EO-00954 Not Available Enquire
Enalaprilat EP Impurity E Impurity CS-EO-00955 Not Available Enquire
Enalaprilat EP Impurity F Impurity CS-EO-00950 90988-18-4 Enquire