Description

Cloprostenol is a potent synthetic prostaglandin analog, widely recognized for its luteolytic and uterotonic properties. This high-purity active pharmaceutical ingredient (API) is critical for ensuring precise and effective reproductive management in veterinary medicine. It is primarily utilized by pharmaceutical manufacturers and veterinary service providers in the animal health industry.

Application

• Veterinary Pharmaceuticals: Primary active ingredient for the induction of parturition (birthing) and treatment of postpartum conditions in livestock.
• Estrus Synchronization: Key component in protocols for synchronizing the estrous cycle in cattle, swine, and horses to improve breeding efficiency.
• Treatment of Pyometra: Used in the management of uterine infections in animals.
• Luteolysis Induction: Facilitates the regression of the corpus luteum to control the reproductive cycle.
• Abortion Induction: Employed for the termination of pregnancy in animals for health or management reasons.
• Research & Development: Serves as a reference standard and key intermediate in pharmacological and biochemical research.

Basic Information

Product Name	Cloprostenol
CAS No.	40665-92-7
Molecular Formula	C22H29ClO6
Molecular Weight	424.91 g/mol
Synonyms	ICI 80996; Estrumate; Cloprostenol Sodium; (5Z)-7-[(1R,2R,3R,5S)-2-[(E,3R)-4-(3-Chlorophenoxy)-3-hydroxybut-1-en-1-yl]-3,5-dihydroxycyclopentyl]hept-5-enoic Acid; PGF2α Analogue; Synthetic Prostaglandin F2α
EINECS	255-011-5

Quality Control

Our Cloprostenol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for assay and related substances, to ensure it meets high-purity standards suitable for pharmaceutical use. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen) at a controlled room temperature of 15-25°C to minimize oxidation and degradation. Keep the container in a dry, cool, and well-ventilated area.

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time corresponds to reference
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single impurity	≤ 0.5%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.