Description

17β-Hydroxyandrosta-1,4-Dien-3-One o-(2,4-Dinitrophenyl)Oxime is a high-purity steroid derivative and a key chemical intermediate in advanced organic synthesis. This compound is valued for its precise molecular structure, which is critical for research and development in specialized pharmaceutical pathways. It is primarily utilized by R&D chemists and manufacturers in the pharmaceutical and fine chemical industries for the synthesis of novel steroid-based compounds and as a reference standard in analytical studies.

Application

• Pharmaceutical Intermediate: A crucial building block in the multi-step synthesis of novel steroid-based active pharmaceutical ingredients (APIs) and drug candidates.
• Research & Development: Serves as a key reference standard and starting material in academic and industrial research focused on steroid chemistry and hormone analog development.
• Fine Chemical Synthesis: Used in the production of complex, high-value specialty chemicals where its specific oxime and dinitrophenyl functional groups are required.
• Analytical Standard: Employed as a certified reference material (CRM) in HPLC, LC-MS, and other chromatographic methods for method development, validation, and quality control.
• Biochemical Research: Investigated for its potential interactions with steroid receptors and enzymes in biochemical and pharmacological studies.

Basic Information

Product Name	17β-Hydroxyandrosta-1,4-Dien-3-One o-(2,4-Dinitrophenyl)Oxime
CAS No.	33514-82-8
Molecular Formula	C25H30N2O5
Molecular Weight	438.52 g/mol
Synonyms	17β-Hydroxyandrosta-1,4-dien-3-one O-(2,4-dinitrophenyl)oxime; Androsta-1,4-dien-17β-ol-3-one 2,4-dinitrophenyloxime; 17β-Hydroxy-1,4-androstadien-3-one O-(2,4-dinitrophenyl)oxime; 1,4-Androstadien-17β-ol-3-one (2,4-dinitrophenyl)oxime; Boldenone DNP-oxime; (17β)-17-Hydroxyandrosta-1,4-dien-3-one O-(2,4-dinitrophenyl)oxime
EINECS	Contact for details

Quality Control

Our 17β-Hydroxyandrosta-1,4-Dien-3-One o-(2,4-Dinitrophenyl)Oxime is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including HPLC for assay and purity, and is supplied with a detailed Certificate of Analysis (COA). We adhere to cGMP principles for pharmaceutical intermediates, ensuring traceability and documentation for research and development applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is light-sensitive (store away from light) and easily oxidized (store under inert atmosphere). For long-term storage, consider storing under an inert gas such as argon or nitrogen in a sealed container.

Specification

Item	Specification
Appearance	Yellow to orange crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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