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(±)-Cloprostenol Sodium Salt CAS NO 55028-72-3


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CAS No.:55028-72-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

(±)-Cloprostenol Sodium Salt is a synthetic prostaglandin analog of the F2α series, widely recognized for its potent luteolytic and smooth muscle-contracting properties. This high-purity active pharmaceutical ingredient (API) is critical for ensuring precise biological activity and formulation stability in veterinary and research applications. It is primarily utilized by manufacturers in the animal health industry and by research institutions focused on reproductive physiology.

Application

  • Veterinary Pharmaceuticals: As the active ingredient in injectable solutions for estrus synchronization and the treatment of reproductive disorders in livestock, such as cattle and swine.
  • Animal Breeding Management: For the controlled induction of parturition (birthing) and termination of pregnancy in various domestic animal species.
  • Biomedical Research: As a critical research tool for studying prostaglandin receptor (FP receptor) function, uterine contractility, and corpus luteum regression in experimental models.
  • API Formulation: Serves as a key starting material or intermediate for compounding pharmacies and manufacturers developing proprietary veterinary therapeutic products.

Basic Information

Product Name (±)-Cloprostenol Sodium Salt
CAS No. 55028-72-3
Molecular Formula C22H28ClNaO6
Molecular Weight 446.90 g/mol
Synonyms Cloprostenol Sodium; Cloprostenol Sodium Salt; (±)-Cloprostenol Na; ICI 80996; Estrumate (Veterinary Trade Name); PGF2α Analogue; Synthetic Prostaglandin F2α; 7-[2-[(3R,5S)-3,5-Dihydroxy-2-[(E,3S)-3-hydroxy-4-[(α,α,α-trifluoro-m-tolyl)oxy]-1-butenyl]cyclopentyl]-5-oxoheptanoic acid sodium salt
EINECS Contact for details

Quality Control

Our (±)-Cloprostenol Sodium Salt is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity, chiral analysis, and residual solvent determination, to ensure it meets stringent specifications for pharmaceutical use. A Certificate of Analysis (COA) detailing identity, purity, and related substances is provided with every shipment to guarantee traceability and batch-to-batch consistency.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and should be handled in a low-humidity environment to prevent degradation.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference
Assay (HPLC) ≥ 98.0% (on anhydrous basis)
Related Substances (HPLC) Total impurities ≤ 2.0%
Water Content (KF) ≤ 5.0%
Residual Solvents (GC) Complies with ICH Q3C
Specific Rotation Contact for details

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

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