Description

Carboprost CAS NO 35700-23-3 is a synthetic prostaglandin analog, specifically a methylated derivative of PGF2α. This compound is a critical active pharmaceutical ingredient (API) valued for its potent uterotonic and luteolytic properties. It is primarily required by pharmaceutical manufacturers and research institutions in the fields of obstetrics, gynecology, and veterinary medicine.

Application

• Pharmaceutical Manufacturing: As the active ingredient in injectable formulations for the treatment of postpartum hemorrhage (PPH) due to uterine atony.
• Therapeutic Abortion: Used in medical procedures for pregnancy termination, particularly in the second trimester.
• Veterinary Medicine: Employed for estrus synchronization and the treatment of pyometra in livestock and companion animals.
• Research & Development: Serves as a key reference standard and biochemical tool in pharmacological studies of prostaglandin receptors and smooth muscle contraction.
• Gynecological Surgery: Used to control bleeding during procedures like cesarean sections or myomectomies.

Basic Information

Item	Detail
Product Name	Carboprost
CAS No.	35700-23-3
Molecular Formula	C₂₁H₃₆O₅
Molecular Weight	368.51 g/mol
Synonyms	Carboprost Tromethamine; (15S)-15-Methylprostaglandin F2α; 15-Methyl-PGF2α; U-32921; Hemabate (brand name for tromethamine salt); Dinolytic (veterinary brand); Prostin/15M
EINECS	Contact for details

Quality Control

Our Carboprost is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) confirming identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as specified on the label. This product is easily oxidized and should be handled under an inert atmosphere when appropriate. Keep the container tightly sealed in a dry, cool, and well-ventilated place.

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%
Single Unknown Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 1.0%

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