Description

Misoprostol is a synthetic prostaglandin E1 analog with significant therapeutic applications. This compound is valued for its potent pharmacological activity, making it a critical active pharmaceutical ingredient (API) in various medical formulations. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of medications for gynecological and gastrointestinal indications.

Application

• Active Pharmaceutical Ingredient (API) in medications for gastric ulcer prophylaxis.
• Key component in obstetric and gynecological pharmaceuticals for labor induction and postpartum hemorrhage management.
• Intermediate in the synthesis of advanced prostaglandin derivatives and related pharmaceutical compounds.
• Reference standard for analytical testing and quality control in pharmaceutical laboratories.
• Research chemical for pharmacological studies involving prostaglandin receptors and pathways.
• Raw material for the development of novel drug delivery systems and combination therapies.

Basic Information

Product Name	Misoprostol
CAS No.	62015-39-8
Molecular Formula	C22H38O5
Molecular Weight	382.54 g/mol
Synonyms	SC-29333; Cytotec; (11α,13E)-11,16-Dihydroxy-16-methyl-9-oxoprost-13-en-1-oic Acid Methyl Ester; Miso; PGE1 Methyl Ester Analog; 16-Methyl PGE1 Methyl Ester; (±)-Misoprostol
EINECS	Contact for details

Quality Control

Our Misoprostol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing specifications such as assay, related substances, and identification are provided to guarantee traceability and compliance with relevant guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its sensitivity to oxidation, it is recommended to store the product under an inert atmosphere for long-term stability. Keep the container tightly sealed in a dry environment to minimize exposure to moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Loss on Drying	≤ 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.