Description

17-α-Hydroxy Progesterone Valerate is a synthetic progestogen derivative, a key pharmaceutical intermediate in the synthesis of more complex steroid hormones. Its primary value lies in its role as a versatile building block for the development of advanced therapeutic agents targeting hormonal regulation. This compound is essential for manufacturers in the pharmaceutical and research and development sectors, particularly those focused on endocrinology and reproductive medicine.

Application

• Pharmaceutical Intermediate: A critical precursor in the multi-step synthesis of potent progestogens and other steroid-based active pharmaceutical ingredients (APIs).
• Research & Development: Used in biochemical research to study progesterone receptor activity and for the development of new hormonal therapies.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
• Chemical Synthesis: Employed in organic synthesis for the structural modification and creation of novel steroid analogs with potential therapeutic applications.

Basic Information

Product Name	17-α-Hydroxy Progesterone Valerate
CAS No.	6677-15-2
Molecular Formula	C26H38O4
Molecular Weight	414.58 g/mol
Synonyms	17α-Hydroxyprogesterone 17-valerate; 17α-Hydroxypregn-4-ene-3,20-dione 17-valerate; 17-Hydroxyprogesterone valerate; Valerate of 17α-Hydroxyprogesterone; 17α-HP Valerate; NSC 97199; Pregn-4-ene-3,20-dione, 17-(1-oxopentyl)oxy)-, (17α)-
EINECS	229-734-8

Quality Control

Our 17-α-Hydroxy Progesterone Valerate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation by IR and NMR. We provide full traceability and detailed Certificates of Analysis (COA) upon request, ensuring compliance with your research or cGMP-grade requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment 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
Assay (HPLC)	≥98.0%
Loss on Drying	≤0.5%
Related Substances (HPLC)	Total impurities ≤2.0%
Single Maximum Impurity	≤0.5%

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