Description

Centchroman is a non-steroidal, selective estrogen receptor modulator (SERM) with a distinct pharmacological profile. This compound is of significant commercial and research interest due to its unique mechanism of action and therapeutic potential. It is primarily utilized by the pharmaceutical industry for research and development, as well as by fine chemical suppliers serving the life sciences sector.

Application

• Pharmaceutical R&D: A key intermediate or active pharmaceutical ingredient (API) in the development of novel therapeutic agents.
• Clinical Research: Used in preclinical and clinical studies investigating its efficacy and safety profile.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Biochemical Research: Employed in studies to understand estrogen receptor interactions and signaling pathways.
• Fine Chemical Synthesis: Acts as a building block for the synthesis of more complex molecules and analogs.

Basic Information

Product Name	Centchroman
CAS No.	31477-60-8
Molecular Formula	C30H35NO2
Molecular Weight	441.61 g/mol
Synonyms	Ormeloxifene; Centron; 67/20; 1-[2-[[4-[(3,4-Dihydro-7-methoxy-2,2-dimethyl-3-phenyl-2H-1-benzopyran-4-yl)phenoxy]ethyl]pyrrolidine; 3,4-Dihydro-2,2-dimethyl-4-(p-(2-(1-pyrrolidinyl)ethoxy)phenyl)-7-methoxy-3-phenyl-2H-1-benzopyran
EINECS	Contact for details

Quality Control

Our Centchroman is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive quality documentation, including detailed Certificates of Analysis (COA) that confirm identity, purity, and impurity profiles. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical applications.

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); ensure the container is kept tightly sealed in a low-humidity environment to maintain stability and prevent degradation.

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%
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.