Description

α-((2-(Dimethylamino)Ethoxy)Methyl)-6-Methyl-2-Naphthalenemethanol Hydrochloride is a high-purity, complex organic compound primarily utilized as a critical pharmaceutical intermediate. Its value lies in its specific molecular architecture, which is essential for the synthesis of advanced active pharmaceutical ingredients (APIs). This compound is particularly relevant for research and manufacturing organizations in the pharmaceutical and life sciences sectors seeking reliable, high-quality building blocks for drug development.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel therapeutic agents, particularly in central nervous system (CNS) and anti-inflammatory drug research.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in multi-step synthetic routes for the production of complex target molecules in GMP manufacturing environments.
• Biochemical Research: Employed as a standard or reagent in pharmacological studies and structure-activity relationship (SAR) investigations.
• Process Development & Scale-up: Critical for process chemistry teams during route optimization and pilot-scale production of new chemical entities (NCEs).
• Reference Standard: Can be supplied as a high-purity standard for analytical method development, validation, and quality control in pharmaceutical laboratories.

Basic Information

Product Name	α-((2-(Dimethylamino)Ethoxy)Methyl)-6-Methyl-2-Naphthalenemethanol Hydrochloride
CAS No.	131963-52-5
Molecular Formula	C17H26ClNO2
Molecular Weight	311.85 g/mol
Synonyms	6-Methyl-2-naphthalenemethanol, α-[(2-(dimethylamino)ethoxy)methyl]-, hydrochloride; (αR)-α-[[2-(Dimethylamino)ethoxy]methyl]-6-methyl-2-naphthalenemethanol hydrochloride; (R)-α-((2-(Dimethylamino)ethoxy)methyl)-6-methyl-2-naphthalenemethanol hydrochloride; Dexlansoprazole Intermediate; Lansoprazole Related Compound; TAK-390 Related Substance; Lanzor Impurity; Prevacid Intermediate
EINECS	Contact for details

Quality Control

Our α-((2-(Dimethylamino)Ethoxy)Methyl)-6-Methyl-2-Naphthalenemethanol Hydrochloride is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis, to ensure it meets the stringent requirements for pharmaceutical R&D and manufacturing. Certificates of Analysis (COA) detailing all specifications are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
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.