Description

6-Dehydro Estradiol 17-Valerate is a synthetic steroid derivative, specifically a valerate ester of 6-dehydroestradiol. This compound is a key pharmaceutical intermediate of significant interest in the research and development of steroidal drugs. It is primarily utilized by manufacturers and research institutions in the pharmaceutical and biotechnology sectors for the synthesis of advanced hormonal agents and for investigative studies in endocrinology.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel steroidal drugs and hormonal therapies.
• Research & Development: Used in biochemical and pharmacological research to study estrogen receptor activity and metabolic pathways.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratory settings.
• API Synthesis: Employed in the development and production of Active Pharmaceutical Ingredients (APIs) for various therapeutic areas.

Basic Information

Product Name	6-Dehydro Estradiol 17-Valerate
CAS No.	1313382-25-0
Molecular Formula	C23H32O3
Molecular Weight	356.50 g/mol
Synonyms	6-Dehydroestradiol 17-valerate; Estra-1,3,5(10),6-tetraene-3,17-diol, 17-valerate; 6-Dehydro-E2-17V; 17-Valeric acid ester of 6-dehydroestradiol; 6-DHE2V
EINECS	Contact for details

Quality Control

Our 6-Dehydro Estradiol 17-Valerate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets exacting standards for research and pharmaceutical use. Certificates of Analysis (COA) detailing all specifications are 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 stability.

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%
Single Unknown Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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