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3-(4-Fluorophenyl)Azetidin-3-Ol Hydrochloride CAS NO 848192-95-0


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CAS No.:848192-95-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

3-(4-Fluorophenyl)Azetidin-3-Ol Hydrochloride is a high-purity, advanced pharmaceutical intermediate characterized by its unique azetidine scaffold. This compound is of significant commercial importance for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs). It is primarily sought after by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development of new therapeutic agents, particularly in central nervous system (CNS) and metabolic disorder research.

Application

  • Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates, particularly those targeting neurological and psychiatric conditions.
  • Medicinal Chemistry Research: Used extensively in lead optimization and structure-activity relationship (SAR) studies due to its constrained azetidine ring system.
  • API Development: Serves as a critical building block for the commercial-scale production of active pharmaceutical ingredients under GMP conditions.
  • Contract Research & Manufacturing (CRO/CMO): Supplied to organizations specializing in custom synthesis and process development for client projects.
  • Academic Research: Utilized in university and institutional labs for exploratory research into new chemical entities and biological pathways.

Basic Information

Product Name 3-(4-Fluorophenyl)Azetidin-3-Ol Hydrochloride
CAS No. 848192-95-0
Molecular Formula C9H10FNO•HCl
Molecular Weight 203.64 g/mol
Synonyms 3-(4-Fluorophenyl)-3-hydroxyazetidine hydrochloride; 3-Hydroxy-3-(4-fluorophenyl)azetidine hydrochloride; 3-(p-Fluorophenyl)-3-hydroxyazetidine HCl; Azetidin-3-ol, 3-(4-fluorophenyl)-, hydrochloride; 848192-95-0; 3-(4-Fluorophenyl)azetidin-3-ol HCl
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Quality Control

Our 3-(4-Fluorophenyl)Azetidin-3-Ol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with every shipment, detailing all relevant specifications. Our quality commitment aligns with the standards expected for pharmaceutical intermediates in development and production.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); containers must be kept tightly sealed to prevent degradation from atmospheric moisture.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Purity (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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