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5α-Androstane-3α,7α,17β-Triol CAS NO 19316-58-6


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CAS No.:19316-58-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

5α-Androstane-3α,7α,17β-Triol CAS NO 19316-58-6 is a high-purity steroid derivative and a key intermediate in the synthesis of specialized pharmaceutical compounds. Its precise stereochemistry and defined structure make it a critical building block for research and development in advanced therapeutic areas. This compound is essential for pharmaceutical manufacturers, research institutions, and fine chemical suppliers focused on endocrinology, metabolic research, and novel drug discovery.

Application

  • Pharmaceutical Intermediate: A crucial precursor in the synthesis of complex steroid-based active pharmaceutical ingredients (APIs) and investigational drugs.
  • Biochemical Research: Used as a reference standard and reagent in metabolic pathway studies, enzyme inhibition assays, and receptor binding research.
  • Endocrinology Studies: Serves as a tool compound for investigating androgen metabolism, steroid hormone biosynthesis, and related physiological processes.
  • Fine Chemical Synthesis: Employed in the multi-step synthesis of other high-value, structurally complex steroidal compounds for various applications.
  • Reference Material: Utilized in analytical laboratories for method development, calibration, and quality control of related steroid analyses.

Basic Information

Product Name 5α-Androstane-3α,7α,17β-Triol
CAS No. 19316-58-6
Molecular Formula C19H32O3
Molecular Weight 308.46 g/mol
Synonyms 5α-Androstane-3α,7α,17β-triol; 3α,7α,17β-Trihydroxy-5α-androstane; Androstanetriol; 5α-Androstan-3α,7α,17β-triol; (3α,5α,7α,17β)-Androstane-3,7,17-triol; Etiocholane-3α,7α,17β-triol
EINECS Contact for details

Quality Control

Our 5α-Androstane-3α,7α,17β-Triol is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to cGMP principles where applicable, and our quality protocols are designed to meet the stringent requirements of pharmaceutical R&D and fine chemical synthesis.

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 hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. For long-term storage, consider using desiccants.

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%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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.

Advanced R&D Expertise

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