share

16Alpha-Ethyl-21-Hydroxy-19-Norpregn-4-Ene-3,20-Dione 21-Laurate CAS NO 67490-00-0


Unit Price:

CAS No.:67490-00-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

16Alpha-Ethyl-21-Hydroxy-19-Norpregn-4-Ene-3,20-Dione 21-Laurate is a high-purity steroid derivative, specifically a laurate ester of a 19-norprogesterone analog. This compound is valued for its role as a critical pharmaceutical intermediate in the synthesis of advanced steroid-based active pharmaceutical ingredients (APIs). It is primarily required by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development of novel therapeutic agents.

Application

  • Pharmaceutical Intermediate: Serves as a key building block in the multi-step synthesis of specialized steroid hormones and related APIs.
  • Steroid Research & Development: Used in academic and industrial R&D laboratories for studying structure-activity relationships (SAR) and developing new drug candidates.
  • Process Chemistry: Employed in scale-up and optimization of synthetic routes for complex steroid molecules in pilot plants and manufacturing facilities.
  • Reference Standard: Can be utilized as a high-purity analytical reference standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name 16Alpha-Ethyl-21-Hydroxy-19-Norpregn-4-Ene-3,20-Dione 21-Laurate
CAS No. 67490-00-0
Molecular Formula C33H52O4
Molecular Weight 512.77 g/mol
Synonyms 19-Nor-16α-ethyl-21-hydroxypregn-4-ene-3,20-dione 21-laurate; 16α-Ethyl-19-norpregn-4-ene-3,20-dione-21-ol laurate; 16α-Ethyl-21-hydroxy-19-norpregn-4-ene-3,20-dione dodecanoate; Gestodene related compound laurate ester; 21-Lauryloxy-16α-ethyl-19-norpregn-4-ene-3,20-dione
EINECS Contact for details

Quality Control

Our 16Alpha-Ethyl-21-Hydroxy-19-Norpregn-4-Ene-3,20-Dione 21-Laurate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the stringent requirements for pharmaceutical intermediates. A detailed Certificate of Analysis (COA) is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain product integrity.

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%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Loss on Drying ≤ 0.5%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

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.