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Remiprostol CAS NO 110845-89-1


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CAS No.:110845-89-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Remiprostol is a synthetic prostaglandin analog with significant biological activity. This compound is valued for its role as a key intermediate and active pharmaceutical ingredient (API) in advanced therapeutic research and development. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on developing treatments for cardiovascular and gastrointestinal disorders. Our supply ensures high purity and batch-to-batch consistency critical for preclinical and clinical studies.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of advanced prostaglandin-based therapeutics.
  • Cardiovascular Research: Used in R&D for studying vascular tone, platelet aggregation, and related physiological pathways.
  • Gastrointestinal Drug Development: Applied in the research of compounds targeting gastric cytoprotection and ulcer healing.
  • Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
  • Biochemical Research: Utilized in cell culture and in vitro studies to investigate prostaglandin receptor interactions and signaling mechanisms.

Basic Information

Item Detail
Product Name Remiprostol
CAS No. 110845-89-1
Molecular Formula C23H38O5
Molecular Weight 394.55 g/mol
Synonyms Remiprostol; 9-Oxo-11α,15S-dihydroxy-17S,20-dimethyl-prosta-5Z,13E-dien-1-oic acid; 11-Deoxy-16-phenoxy-17,18,19,20-tetranor-PGE2; ZK 96 480; Prostaglandin E1 analog; 17S,20-Dimethyl PGE1
EINECS Contact for details

Quality Control

Every batch of Remiprostol is manufactured and tested under a strict quality management system. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and conformity to specifications. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with each shipment. We support development and commercial projects requiring material that meets GMP-grade standards for advanced pharmaceutical applications.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen) at controlled room temperature (15-25°C) or as specified on the label. This material is easily oxidized and light-sensitive; prolonged exposure to air or light should be avoided to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white 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 ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Water Content (KF) ≤ 0.5%

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

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

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