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Gestrinonemethylnorgestrienone CAS NO 40542-65-2


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CAS No.:40542-65-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Gestrinonemethylnorgestrienone is a synthetic steroid compound of significant interest in advanced pharmaceutical research and development. Its unique structural features make it a valuable intermediate for the synthesis of novel therapeutic agents, particularly in the field of endocrinology. This high-purity compound is primarily utilized by research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development of hormone-related therapies and reference standards.

Application

  • Pharmaceutical Intermediate: A key building block in the synthesis of advanced steroid-based active pharmaceutical ingredients (APIs).
  • Research & Development: Used as a reference standard and starting material in medicinal chemistry for exploring new hormonal pathways and receptor interactions.
  • Biochemical Studies: Employed in in vitro and in vivo studies to investigate steroid metabolism, pharmacokinetics, and pharmacodynamics.
  • Fine Chemical Synthesis: Serves as a precursor for the production of specialized steroid derivatives with potential therapeutic applications.
  • Analytical Reference: Provides a high-purity standard for quality control laboratories to calibrate instruments like HPLC and GC-MS for steroid analysis.

Basic Information

Product Name Gestrinonemethylnorgestrienone
CAS No. 40542-65-2
Molecular Formula C21H26O2
Molecular Weight 310.43 g/mol
Synonyms 13-Ethyl-17-hydroxy-11-methylene-18,19-dinor-17α-pregna-4,9-dien-20-yn-3-one; Gestrinone Impurity; 11-Methylenonorgestrienone; δ9(11)-Dehydrogenestrinone; 17α-Ethynyl-17β-hydroxy-11-methylenestra-4,9-dien-3-one; 11-Methylene-19-nor-17α-pregna-4,9-dien-20-yn-17-ol-3-one
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Quality Control

Our Gestrinonemethylnorgestrienone 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 as determined by advanced analytical techniques including HPLC, GC-MS, and NMR. We adhere to cGMP guidelines where applicable to meet the stringent requirements of the pharmaceutical and research industries.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to minimize exposure to atmospheric moisture. For long-term storage, consider the use of desiccants.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Single Unknown Impurity (HPLC) ≤ 0.5%
Total Impurities (HPLC) ≤ 2.0%

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.

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