Description

Trestolone Acetate is a synthetic androgen and anabolic steroid (AAS) derivative. This high-purity compound is critical for pharmaceutical research and development, particularly in the study of androgen receptor-mediated pathways. It is primarily utilized by research institutions, pharmaceutical companies, and reference standard producers for analytical and developmental purposes.

Application

• Pharmaceutical R&D: Serves as a key intermediate or reference standard in the development of novel androgen-based therapies.
• Biochemical Research: Used in in vitro and in vivo studies to investigate androgen receptor binding, activation, and downstream biological effects.
• Metabolic Studies: Employed in research focused on the metabolism, pharmacokinetics, and pharmacodynamics of anabolic steroids.
• Analytical Standard: Acts as a certified reference material (CRM) for quality control and method validation in analytical laboratories using techniques like HPLC and LC-MS.
• Endocrinology Research: A tool for studying hormonal regulation, muscle protein synthesis, and related physiological processes.

Basic Information

Product Name	Trestolone Acetate
CAS No.	6157-87-5
Molecular Formula	C22H32O3
Molecular Weight	344.49 g/mol
Synonyms	7α-Methyl-19-nortestosterone 17β-acetate; MENT Acetate; 7α-Methylestr-4-en-17β-ol-3-one 17-acetate; Trestolone 17-acetate; 7α-Methyl-19-norandrost-4-en-17β-ol-3-one 17-acetate
EINECS	Contact for details

Quality Control

Our Trestolone Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets exacting standards for research use. A detailed Certificate of Analysis (COA) is provided with every shipment, guaranteeing traceability and consistency.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a desiccated 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%
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.