Description

Abiraterone Related Compound 2 (Prasterone Triflate) is a high-purity chemical reference standard and synthetic intermediate of significant importance in pharmaceutical development and quality control. This compound is critical for ensuring the accuracy and reliability of analytical methods used in the manufacturing and testing of active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions, pharmaceutical companies, and quality assurance laboratories involved in the development and production of steroid-based therapeutics.

Application

• Pharmaceutical Reference Standard: Serves as a critical impurity marker and system suitability standard in the HPLC/LC-MS analysis of Abiraterone Acetate and related drug substances.
• Process Chemistry Research: Used as a key intermediate or a model compound in the research and development of novel synthetic pathways for steroidal drugs.
• Quality Control & Assurance: Essential for method validation, impurity profiling, and establishing specification limits to comply with ICH Q3A/B guidelines in API manufacturing.
• Metabolite Studies: Employed in pharmacological and toxicological research to study drug metabolism and degradation pathways.
• Regulatory Documentation: Provides certified material for inclusion in regulatory submission dossiers (e.g., for FDA, EMA) to support drug approval processes.

Basic Information

Product Name	Abiraterone Related Compound 2 (Prasterone Triflate)
CAS No.	124643-35-2
Molecular Formula	C22H31F3O4S
Molecular Weight	448.55 g/mol
Synonyms	Prasterone Triflate; Dehydroepiandrosterone Trifluoromethanesulfonate; DHEA Triflate; 3β-Hydroxyandrost-5-en-17-one Triflate; (3β)-3-Hydroxyandrost-5-en-17-yl Trifluoromethanesulfonate; Abiraterone Impurity; Abiraterone Related Substance 2; Steroid Triflate Intermediate
EINECS	Contact for details

Quality Control

Every batch of Abiraterone Related Compound 2 is manufactured and tested under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency meet the exacting standards required for pharmaceutical research and development. A comprehensive Certificate of Analysis (COA) detailing all test results and specifications is provided with each shipment to support your regulatory and quality needs.

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 should be handled in a dry environment to prevent degradation. For long-term storage, consider desiccant or inert atmosphere conditions.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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