share

Fenprostalene CAS NO 69381-94-8


Unit Price:

CAS No.:69381-94-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fenprostalene CAS NO 69381-94-8 is a synthetic prostaglandin analog, a high-purity active pharmaceutical ingredient (API) designed for advanced veterinary and research applications. Its primary value lies in its potent luteolytic activity, enabling precise control of the reproductive cycle in livestock. This compound is essential for manufacturers and research institutions focused on animal health, fertility management, and the development of veterinary pharmaceuticals. We supply it with a commitment to stringent quality control and reliable global distribution.

Application

  • Veterinary Pharmaceuticals: Core active ingredient for injectable solutions used to synchronize estrus and induce parturition in cattle and swine.
  • Livestock Fertility Management: Key component in protocols for timed artificial insemination (TAI) to improve breeding efficiency and herd productivity.
  • Research & Development: Used as a reference standard in biochemical research and for developing new therapeutic agents targeting prostaglandin receptors.
  • Veterinary Clinical Studies: Employed in controlled trials to evaluate efficacy and safety profiles for new reproductive health treatments.
  • API Formulation: Sourced by pharmaceutical companies for the GMP-compliant manufacture of finished dosage forms.
  • Animal Health Product Development: Integral to creating innovative solutions for managing reproductive disorders in production animals.

Basic Information

Product Name Fenprostalene
CAS No. 69381-94-8
Molecular Formula C23H34O5
Molecular Weight 390.51 g/mol
Synonyms Fenprostalene; BOVILENE; ICI-81008; RS-84043; (Z)-7-[(1R,2R,3R,5S)-2-[(E,3S)-3-Hydroxy-4-phenoxy-1-butenyl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid; Prostaglandin F2α analog; Synthetic PGF2α
EINECS Contact for details

Quality Control

Our Fenprostalene is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis. We provide a detailed Certificate of Analysis (COA) with each shipment, ensuring traceability and compliance with relevant industry standards for pharmaceutical intermediates. Our quality commitment supports your requirements for GMP-grade materials.

Storage

Preserve in a tightly closed container, protected from light. Store in a freezer at -20°C to -10°C under an inert atmosphere (e.g., nitrogen or argon) to prevent oxidation. Allow the sealed container to reach room temperature before opening to minimize moisture condensation. Keep away from strong oxidizing agents.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Water Content (KF) ≤ 0.5%
Specific Rotation Contact for details

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.