Description

n-(3-(Oleoyloxy)Androst-5-En-17-Yl(Pentyloxycarbonyl))-n-n-Bis(2-Chloroethyl)Amine is a sophisticated steroidal derivative designed for advanced pharmaceutical and biochemical research. This compound is valued for its unique molecular architecture, which combines a steroidal backbone with functional groups that enable targeted chemical interactions. It serves as a critical intermediate or active pharmaceutical ingredient (API) for researchers and manufacturers developing novel therapeutic agents. The product is supplied to meet the stringent quality demands of the global life sciences sector.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel steroidal drugs and hormone-based therapies.
• Biochemical Research: Used as a reference standard or probe in studies investigating steroidal pathways and receptor interactions.
• API Development: Serves as an active pharmaceutical ingredient (API) or precursor in the development of targeted cancer treatments and other specialized medications.
• Chemical Synthesis: A versatile intermediate for creating more complex molecules with specific biological activities in medicinal chemistry.
• Laboratory Reagent: Employed in analytical and research laboratories for method development and validation.

Basic Information

Product Name	n-(3-(Oleoyloxy)Androst-5-En-17-Yl(Pentyloxycarbonyl))-n-n-Bis(2-Chloroethyl)Amine
CAS No.	90343-98-9
Molecular Formula	C48H79Cl2NO5
Molecular Weight	845.04 g/mol (Contact for details)
Synonyms	N-[3-(Oleoyloxy)androst-5-en-17-yl(pentyloxycarbonyl)]-N,N-bis(2-chloroethyl)amine; 90343-98-9; Androst-5-ene-17-carboxamide, N,N-bis(2-chloroethyl)-3-[(1-oxo-9-octadecenyl)oxy]-, 17-pentyl ester, (3β,17β)-; Oleoyloxy Androstene Derivative; Steroidal Nitrogen Mustard Ester; Pentyl Ester of Steroidal Amine.
EINECS	Contact for details

Quality Control

Our n-(3-(Oleoyloxy)Androst-5-En-17-Yl(Pentyloxycarbonyl))-n-n-Bis(2-Chloroethyl)Amine is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with every shipment, detailing all critical parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your most sensitive applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 97.0%
Related Substances (HPLC)	Total impurities ≤ 3.0%
Any single impurity	≤ 1.0%
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.