Description

17Beta-Hydroxyandrost-4-En-3-One Hexanoate is a synthetic steroid ester, specifically the hexanoate ester of testosterone. This compound is a key pharmaceutical intermediate used in the synthesis of long-acting testosterone derivatives and other advanced steroid-based therapeutics. It is essential for manufacturers in the pharmaceutical and research sectors requiring high-purity steroid building blocks for hormone replacement therapies and performance-enhancing drug development. Our supply ensures consistent quality and reliable availability for critical production and R&D processes.

Application

• Pharmaceutical Intermediate: Primary building block for the synthesis of testosterone cypionate, testosterone enanthate, and other long-acting injectable androgen formulations.
• Hormone Replacement Therapy (HRT) Research: Used in the development and production of controlled-release drug delivery systems for treating male hypogonadism.
• Veterinary Medicine: Employed in the formulation of anabolic agents for growth promotion and therapeutic applications in livestock.
• Reference Standard: Serves as a certified reference material (CRM) for quality control and analytical method development in pharmaceutical laboratories.
• Biochemical Research: Utilized in metabolic studies and receptor binding assays to investigate androgen pathways and steroid metabolism.
• Performance-Enhancing Compound Synthesis: A critical precursor in the controlled synthesis of anabolic-androgenic steroids (AAS) for clinical and research purposes.

Basic Information

Product Name	17Beta-Hydroxyandrost-4-En-3-One Hexanoate
CAS No.	10312-45-5
Molecular Formula	C25H38O3
Molecular Weight	386.57 g/mol
Synonyms	Testosterone Hexanoate; 17β-Hydroxyandrost-4-en-3-one 17-hexanoate; Androst-4-en-3-one, 17-(1-oxohexyl)oxy)-, (17β)-; Testosterone Caproate; NSC 17591; Testosterone 17-hexanoate; 3-Oxoandrost-4-en-17β-yl hexanoate
EINECS	Contact for details

Quality Control

Every batch of 17Beta-Hydroxyandrost-4-En-3-One Hexanoate is manufactured and tested under strict quality management systems. We provide comprehensive analytical data to ensure the material meets the high-purity standards required for pharmaceutical synthesis and research. A detailed Certificate of Analysis (COA) is supplied with each shipment, confirming identity, purity, and impurity profiles as determined by HPLC, GC, and spectroscopic methods.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions 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%
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.