Description

6β-Hydroxy-Oral Turinabol is a synthetic anabolic-androgenic steroid (AAS) derivative, specifically a hydroxylated metabolite of Oral Turinabol (Chlorodehydromethyltestosterone). This compound is of significant interest in pharmaceutical research and development for its metabolic profile and potential applications in studying steroid pathways. It serves as a critical reference standard and intermediate for researchers and manufacturers in the pharmaceutical, analytical, and life science sectors who require high-purity compounds for method development, metabolism studies, and quality control.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the qualitative and quantitative analysis of anabolic steroids in drug testing, anti-doping control, and forensic toxicology.
• Metabolite Research: Serves as a key metabolite for in-vitro and in-vivo studies investigating the biotransformation, pharmacokinetics, and excretion profiles of Oral Turinabol.
• Analytical Method Development: Essential for developing and validating sensitive analytical methods such as LC-MS/MS, GC-MS, and HPLC for the detection of steroids in complex biological matrices.
• Biochemical Research: Utilized in studies exploring the structure-activity relationships (SAR) of anabolic steroids and their interactions with androgen receptors.
• Quality Control (QC) & Assurance: Employed by pharmaceutical and supplement manufacturers to verify the purity of products and screen for specific metabolites or impurities.

Basic Information

Product Name	6β-Hydroxy-Oral Turinabol
CAS No.	25486-01-5
Molecular Formula	C₂₁H₂₉ClO₃
Molecular Weight	364.91 g/mol
Synonyms	6β-Hydroxy-4-chloro-17α-methyl-17β-hydroxyandrost-1,4-dien-3-one; 6β-Hydroxychlorodehydromethyltestosterone; 6β-Hydroxy CDMT; 6β-OH-Turinabol; 6β-Hydroxy-1-dehydro-4-chloromethyltestosterone; 4-Chloro-6β,17β-dihydroxy-17α-methylandrosta-1,4-dien-3-one
EINECS	Contact for details

Quality Control

Our 6β-Hydroxy-Oral Turinabol is manufactured under strict quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC for purity, MS and NMR for structural confirmation, and residual solvent analysis to ensure it meets high-purity standards suitable for research applications. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting the specific results for 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). The product is light-sensitive and should be handled accordingly to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residual Solvents (GC)	Complies with ICH guidelines

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