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Rac-11-Deoxy-8(12)-Dehydro Misoprostol CAS NO 1331639-92-9


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CAS No.:1331639-92-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Rac-11-Deoxy-8(12)-Dehydro Misoprostol is a synthetic prostaglandin analog and a key intermediate in advanced pharmaceutical research and development. This compound is valued for its structural relevance in the synthesis of novel therapeutic agents targeting specific prostaglandin receptors. It is primarily utilized by research institutions and pharmaceutical companies engaged in the development of new drug candidates, particularly in areas such as gastroenterology and reproductive health. The material is supplied with a focus on high purity and batch-to-batch consistency to support critical R&D and scale-up processes.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of proprietary prostaglandin-based drug candidates.
  • Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to explore and optimize biological activity profiles.
  • Reference Standard: Employed as an analytical standard in method development and quality control for related pharmaceutical products.
  • Process Development: Supports route scouting and optimization for the efficient, scalable production of target molecules.
  • Academic Research: Facilitates biochemical and pharmacological studies in university and institutional laboratories.

Basic Information

Product Name Rac-11-Deoxy-8(12)-Dehydro Misoprostol
CAS No. 1331639-92-9
Molecular Formula C₂₂H₃₈O₅
Molecular Weight 382.54 g/mol
Synonyms 11-Deoxy-8(12)-dehydro Misoprostol; rac-11-Deoxy-8(12)-dehydro Misoprostol; (11R,16S)-11,16-Dihydroxy-16-methyl-9-oxoprosta-5,13-dien-1-oic acid methyl ester; Misoprostol Impurity; Misoprostol Related Compound; Prostaglandin E1 Analog; SC-30695 Impurity
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Quality Control

Our Rac-11-Deoxy-8(12)-Dehydro Misoprostol is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for pharmaceutical research. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all critical quality attributes. We support compliance with cGMP guidelines for advanced intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at a controlled room temperature (15-25°C) to minimize oxidation and degradation. The container should be kept in a cool, dry, and well-ventilated area away from heat sources and incompatible materials.

Specification

Item Specification
Appearance White to off-white solid
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Purity (HPLC) ≥ 98.0%
Water Content (KF) ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm

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

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