Description

2,6-Dichloro-4-(Difluoromethoxy)Benzyl Alcohol is a high-purity, advanced pharmaceutical intermediate characterized by its unique halogenated benzyl alcohol structure. This compound is critical for the synthesis of complex active pharmaceutical ingredients (APIs), particularly in modern agrochemical and pharmaceutical research. It is primarily sought after by R&D chemists and process development scientists in the life sciences sector for constructing novel molecular architectures.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, especially those targeting central nervous system and metabolic disorders.
• Agrochemical Synthesis: Used in the research and development of next-generation herbicides and pesticides, leveraging its difluoromethoxy and dichloro substituents.
• Chemical Research & Development: Serves as a versatile synthon for introducing the 2,6-dichloro-4-(difluoromethoxy)benzyl moiety into more complex molecules.
• Material Science Precursor: Potential use in the development of specialty polymers and advanced organic materials requiring specific halogenated aromatic units.
• Contract Manufacturing (CMO): Supplied to custom synthesis organizations for scale-up and production under cGMP guidelines for clinical trial materials.

Basic Information

Product Name	2,6-Dichloro-4-(Difluoromethoxy)Benzyl Alcohol
CAS No.	1806276-05-0
Molecular Formula	C9H8Cl2F2O2
Molecular Weight	265.06 g/mol
Synonyms	2,6-Dichloro-4-(difluoromethoxy)benzenemethanol; [2,6-Dichloro-4-(difluoromethoxy)phenyl]methanol; 4-(Difluoromethoxy)-2,6-dichlorobenzyl Alcohol; (2,6-Dichloro-4-(difluoromethoxy)phenyl)methanol; Benzyl alcohol, 2,6-dichloro-4-(difluoromethoxy)-; CAS 1806276-05-0
EINECS	Contact for details

Quality Control

Our 2,6-Dichloro-4-(Difluoromethoxy)Benzyl Alcohol is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, GC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. Certificates of Analysis (COA) are provided with each shipment, detailing all critical quality attributes. We support development and commercial projects with material suitable for research use and can supply grades aligned with ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at controlled room temperature (15-25°C). The compound may be hygroscopic (moisture-sensitive); keep the container tightly sealed under an inert atmosphere if necessary. Keep away from strong oxidizing agents, strong acids, and strong bases.

Specification

Item	Specification
Appearance	White to off-white crystalline 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%
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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