share

(R) (+) Dichlorophenyl Amino Alcohol CAS NO 135936-36-6


Unit Price:

CAS No.:135936-36-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

(R) (+) Dichlorophenyl Amino Alcohol is a high-value chiral intermediate and building block in organic synthesis. This compound matters for its role in creating enantiomerically pure active pharmaceutical ingredients (APIs) and advanced agrochemicals. It is primarily needed by research institutions and manufacturers in the pharmaceutical, agrochemical, and fine chemical industries for developing new therapeutic agents and specialty products.

Application

  • Key chiral intermediate in the synthesis of pharmaceutical APIs, particularly for central nervous system (CNS) and cardiovascular drugs.
  • Building block for the production of advanced agrochemicals, including herbicides and fungicides with specific stereochemical activity.
  • Precursor in the manufacture of liquid crystals and other advanced electronic materials.
  • Starting material for asymmetric catalysis and the development of novel chiral ligands.
  • Intermediate for custom synthesis and contract research organization (CRO) projects in medicinal chemistry.
  • Used in academic and industrial research for studying structure-activity relationships (SAR).

Basic Information

Item Details
Product Name (R) (+) Dichlorophenyl Amino Alcohol
CAS No. 135936-36-6
Molecular Formula C8H9Cl2NO
Molecular Weight 206.07 g/mol
Synonyms (R)-2-Amino-1-(2,4-dichlorophenyl)ethanol; (R)-(+)-2-Amino-1-(2,4-dichlorophenyl)ethanol; (R)-1-(2,4-Dichlorophenyl)-2-aminoethanol; (R)-2,4-Dichloro-β-aminoethylbenzene; (R)-2,4-DCPAE; (R)-Dichlorophenyl Ethanolamine; (R)-Amino Alcohol Intermediate; (R)-enantiomer of Dichlorophenyl Amino Alcohol
EINECS Contact for details

Quality Control

Our (R) (+) Dichlorophenyl Amino Alcohol is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including chiral purity analysis, to ensure it meets the high standards required for pharmaceutical and fine chemical applications. Certificates of Analysis (COA) detailing purity, enantiomeric excess, and impurity profiles are available upon request.

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). Due to its hygroscopic nature, the container must be kept tightly sealed to exclude moisture. Keep away from incompatible materials such as strong oxidizing agents.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Enantiomeric Excess (Chiral HPLC) ≥ 99.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 10 ppm
Related Substances (HPLC) Individual impurity ≤ 0.5%; Total impurities ≤ 1.0%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

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

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.