Description

Dihydroproscar is a high-purity pharmaceutical intermediate and active ingredient with the CAS registry number 98319-24-5. This compound is critical for ensuring the quality and efficacy of advanced therapeutic formulations. It is primarily utilized by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development and production of specialized medications.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for therapeutic applications.
• Research & Development: Used in biochemical and pharmacological research to study enzyme interactions and metabolic pathways.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development and quality control in laboratories.
• Active Ingredient: Employed in the formulation of specific prescription medications targeting hormonal pathways.
• Process Chemistry: Integral to scalable, GMP-compliant manufacturing processes for final drug products.

Basic Information

Product Name	Dihydroproscar
CAS No.	98319-24-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Dutasteride Impurity; Dihydrofinasteride; 4-Aza-5α-androst-1-ene-3-one, 17β-(1,1-dimethylethyl)carbamoyl]-; Finasteride Impurity; 17β-N-tert-Butylcarbamoyl-4-aza-5α-androst-1-en-3-one; Dihydro Finasteride; Dutasteride Related Compound; 98319-24-5
EINECS	Contact for details

Quality Control

Our Dihydroproscar is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC and spectroscopic methods, to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which may affect stability and performance.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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