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

Celiprololhydrochloride Related Compounds

Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Celiprolol EP Impurity B Impurity CS-O-13432 125579-40-0 Enquire
Celiprolol EP Impurity C Impurity CS-O-13433 57471-01-9 Enquire
Celiprolol EP Impurity F Impurity CS-O-13436 79881-89-3 Enquire
Celiprolol EP Impurity G Impurity CS-O-13437 56980-98-4 Enquire
Celiprolol EP Impurity H Impurity CS-O-13438 85045-98-3 Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
4-Nitrophenyl Acetate Intermediate CS-T-59461 830-03-5 In Stock