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(+)-Cloprostenol Sodium CAS NO 62561-03-9


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CAS No.:62561-03-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

(+)-Cloprostenol Sodium CAS NO 62561-03-9 is the sodium salt of a potent synthetic prostaglandin analog. This high-purity active pharmaceutical ingredient (API) is critical for its targeted biological activity in veterinary and research applications. It is primarily required by manufacturers in the animal health sector and by research institutions conducting studies in reproductive biology and physiology.

Application

  • Veterinary Pharmaceuticals: Key active ingredient in formulations for estrus synchronization and the treatment of reproductive disorders in livestock, particularly cattle and horses.
  • Animal Breeding Management: Used to induce parturition (birthing) at a predetermined time, facilitating better herd management and veterinary care.
  • Research & Development: A vital tool in biochemical and pharmacological research for studying prostaglandin receptors, signaling pathways, and reproductive endocrinology.
  • Veterinary Clinical Practice: Employed by veterinarians for therapeutic termination of pregnancy and treatment of chronic endometritis (pyometra) in small and large animals.
  • API Synthesis: Serves as a critical intermediate or starting material for the synthesis of more complex prostaglandin-based compounds.

Basic Information

Product Name (+)-Cloprostenol Sodium
CAS No. 62561-03-9
Molecular Formula C22H28ClO6Na
Molecular Weight 446.90 g/mol
Synonyms (+)-Cloprostenol Sodium Salt; Cloprostenol Sodium; D-Cloprostenol Sodium; (5Z)-7-[(1R,2R,3R,5S)-2-[(E)-3-Chloro-4-(3-chlorophenoxy)-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid Sodium Salt; Estrumate (Veterinary Trade Name); 62561-03-9; ICI 80996; PGF2α analog sodium salt
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Quality Control

Our (+)-Cloprostenol Sodium is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity and chiral purity, residual solvent analysis, and identification by IR and NMR, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) documenting full compliance are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at 2-8°C. This product is hygroscopic (moisture-sensitive) and must be kept under inert atmosphere or in a desiccator after opening to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0% (on anhydrous basis)
Chiral Purity (HPLC) ≥ 99.0%
Water Content (KF) ≤ 2.0%
Residual Solvents (GC) Meets ICH Q3C guidelines
Heavy Metals ≤ 20 ppm

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

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