Description

Durabolin Oxime is a high-purity chemical intermediate of significant interest in advanced pharmaceutical synthesis. This compound is valued for its role as a key building block in the development of specialized anabolic agents and other pharmacologically active molecules. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development and production of steroid-based therapeutics and reference standards.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of anabolic steroids and related therapeutic compounds.
• Research & Development: Used in academic and industrial laboratories for pharmacological studies and the development of new chemical entities.
• Reference Standard: Serves as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical manufacturing.
• Metabolite Studies: Employed in the research of drug metabolism and pharmacokinetics (DMPK) for related steroid compounds.

Basic Information

Product Name	Durabolin Oxime
CAS No.	82332-16-9
Molecular Formula	C20H31NO2
Molecular Weight	317.47 g/mol
Synonyms	19-Norandrost-4-en-3-one, 17-(1-oxobutoxy)-, oxime; Nandrolone Oxime; 19-Nortestosterone 17β-propionate oxime; 17β-Hydroxyestr-4-en-3-one propionate oxime; Norandrostenolone propionate oxime; Durabolin Oxime; Nandrolone 17-propionate oxime
EINECS	Contact for details

Quality Control

Our Durabolin Oxime is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant industry guidelines to support our clients' regulatory and research requirements.

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 product integrity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%

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