Description

(20S)-4,4,14-Trimethyl-3β,20-Bis(Dimethylamino)-9β,19-Cyclo-5α-Pregnan-16α-Ol is a high-purity, structurally complex steroid derivative characterized by its unique 9β,19-cyclo-pregnane framework and dual dimethylamino functional groups. This compound is of significant interest in advanced pharmaceutical research and development due to its potential as a key synthetic intermediate or a pharmacologically active scaffold. It is primarily utilized by research institutions, pharmaceutical companies, and fine chemical manufacturers engaged in steroid chemistry, medicinal chemistry, and the synthesis of novel therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of novel steroid-based drug candidates.
• Medicinal Chemistry Research: Used as a reference standard or a starting material for structure-activity relationship (SAR) studies to develop new therapeutic molecules.
• Biochemical Research: Employed in studies investigating steroid hormone receptor interactions or enzyme inhibition mechanisms.
• Fine Chemical Synthesis: Acts as a specialized precursor for the production of high-value, complex organic molecules in custom synthesis projects.
• Academic Research: Utilized in university and institutional laboratories for advanced organic synthesis and chemical methodology development.

Basic Information

Product Name	(20S)-4,4,14-Trimethyl-3β,20-Bis(Dimethylamino)-9β,19-Cyclo-5α-Pregnan-16α-Ol
CAS No.	808-94-6
Molecular Formula	C₂₈H₅₀N₂O
Molecular Weight	430.71 g/mol
Synonyms	16α-Hydroxy-4,4,14-trimethyl-3β,20-bis(dimethylamino)-9β,19-cyclo-5α-pregnane; 3β,20-Bis(dimethylamino)-9β,19-cyclo-5α-pregnan-16α-ol; 9β,19-Cyclopregnan-16α-ol derivative; (20S)-4,4,14-Trimethyl-3β,20-bis(dimethylamino)-9β,19-cyclo-5α-cholestan-16α-ol (related system); 16α-Hydroxy-9β,19-cyclolanostane derivative
EINECS	Contact for details

Quality Control

Our (20S)-4,4,14-Trimethyl-3β,20-Bis(Dimethylamino)-9β,19-Cyclo-5α-Pregnan-16α-Ol is manufactured under strict quality control protocols to ensure high purity and batch-to-batch consistency, suitable for demanding research applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP principles where applicable, and our quality systems are designed to meet the stringent requirements of the pharmaceutical and biotechnology industries.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The compound is light-sensitive (store away from light). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
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.