Description

Femovan is a high-purity pharmaceutical intermediate and active ingredient, identified by CAS No. 109852-02-0. This compound is critical for ensuring the efficacy and consistency of advanced therapeutic formulations. It is primarily utilized by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development and production of specialized medications.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for hormonal therapies.
• Research & Development: Used in biochemical research for studying receptor interactions and developing new therapeutic agents.
• Steroid Synthesis: Serves as a precursor in the multi-step synthesis of complex steroid-based compounds.
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in laboratories.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.

Basic Information

Item	Detail
Product Name	Femovan
CAS No.	109852-02-0
Molecular Formula	C24H32O4
Molecular Weight	384.51 g/mol
Synonyms	Femovan; 3-Hydroxy-19-nor-17α-pregna-1,3,5(10)-trien-20-yn-17-ol; 17α-Ethynyl-19-norandrosta-1,3,5(10)-triene-3,17β-diol; 19-Nor-17α-pregna-1,3,5(10)-trien-20-yne-3,17-diol; Tibolone Impurity; Tibolone Related Compound A; Org OD-14 Impurity
EINECS	Contact for details

Quality Control

Our Femovan is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets exacting standards for pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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 low-humidity environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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