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16Alpha,17Alpha-Dimethylprogesterone CAS NO 19590-23-9


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CAS No.:19590-23-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

16Alpha,17Alpha-Dimethylprogesterone is a synthetic progestogen derivative, a key intermediate in the synthesis of advanced steroid-based pharmaceuticals. Its value lies in its specific stereochemistry, which is crucial for developing potent and selective therapeutic agents targeting hormone receptors. This high-purity intermediate is essential for pharmaceutical R&D and manufacturing, particularly for organizations developing novel treatments in endocrinology, oncology, and reproductive health.

Application

  • Pharmaceutical Intermediate: A critical building block in the multi-step synthesis of advanced steroid drugs and active pharmaceutical ingredients (APIs).
  • Hormone Receptor Research: Used in biochemical and pharmacological studies to investigate progestogen receptor binding and activity.
  • Steroid Analog Development: Serves as a precursor for creating novel steroid analogs with modified biological profiles for therapeutic applications.
  • Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
  • Academic & Industrial R&D: Utilized in research institutions and corporate R&D departments for exploring new synthetic pathways and drug candidates.

Basic Information

Item Detail
Product Name 16Alpha,17Alpha-Dimethylprogesterone
CAS No. 19590-23-9
Molecular Formula C23H34O2
Molecular Weight 342.52 g/mol
Synonyms 16α,17α-Dimethylprogesterone; 16α,17α-Dimethylpregn-4-ene-3,20-dione; 16,17-Dimethylprogesterone; (8R,9S,10R,13S,14S,16R,17R)-16,17-Dimethyl-13-methyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene-3,20(2H)-dione
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Quality Control

Our 16Alpha,17Alpha-Dimethylprogesterone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the stringent requirements of pharmaceutical development. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting the specific results for that lot.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled and stored accordingly to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Loss on Drying ≤ 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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