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

Estradiol Valerate Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
17-Beta-Estradiol-16 Stable Isotopes CS-O-10121 79037-37-9 In Stock


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Estradiol Valerate API Standards CS-O-01448A Not Available Enquire
Estradiol Valerate API Standards CS-O-14664 979-32-8 In Stock


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
1-Methylestrone Impurities CS-T-81956 4011-48-7 Enquire
4-Methyl Estradiol Valerate Impurities CS-P-07807 1359847-37-2 Enquire
Estradiol Valerate Impurities CS-0-14664 979-32-8 In Stock
Estradiol valerate EP Impurity I Impurities CS-EO-00888 Not Available Enquire
ESTRADIOL VALERATE EP IMPURITY J Impurities CS-P-08554 Not Available Enquire