Description

4-(2-(tert-Butylamino)-1-Hydroxyethyl)-2-Methylphenol Hydrochloride is a high-purity, synthetically derived organic compound of significant interest in advanced chemical synthesis. This compound matters as a key chiral intermediate and building block for the development of complex molecules, offering precise structural control. It is primarily needed by research institutions and manufacturers in the pharmaceutical and agrochemical industries for the synthesis of active ingredients and fine chemicals.

Application

• Pharmaceutical Intermediate: A critical chiral building block for the synthesis of β-adrenergic receptor agonists and other active pharmaceutical ingredients (APIs).
• Agrochemical Synthesis: Used in the research and production of advanced crop protection agents and herbicides.
• Fine Chemical Production: Serves as a precursor in the manufacture of specialty chemicals and complex organic molecules.
• Biochemical Research: Employed in life science research for studying receptor-ligand interactions and metabolic pathways.
• Asymmetric Synthesis: Utilized as a key intermediate in stereoselective synthesis due to its chiral centers.
• Reference Standard: Supplied as a high-purity analytical standard for quality control and method development in laboratories.

Basic Information

Item	Detail
Product Name	4-(2-(tert-Butylamino)-1-Hydroxyethyl)-2-Methylphenol Hydrochloride
CAS No.	70334-18-8
Molecular Formula	C13H22ClNO2
Molecular Weight	259.77 g/mol
Synonyms	2-Methyl-5-[1-hydroxy-2-[(1,1-dimethylethyl)amino]ethyl]phenol hydrochloride; (R*,S*)-(±)-5-[1-Hydroxy-2-(tert-butylamino)ethyl]-o-cresol hydrochloride; Terbutaline Impurity B (Hydrochloride); (±)-Terbutaline Related Compound B HCl; 1-(3-Hydroxy-2-methyl-5-((tert-butylamino)methyl)phenyl)ethan-1-ol hydrochloride; 5-[1-Hydroxy-2-(tert-butylamino)ethyl]-2-methylphenol hydrochloride; rac-Terbutaline impurity B HCl
EINECS	Contact for details

Quality Control

Our 4-(2-(tert-Butylamino)-1-Hydroxyethyl)-2-Methylphenol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and chiral purity analysis, to ensure compliance with stringent specifications for pharmaceutical-grade intermediates. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

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 prevent moisture absorption. Keep away from incompatible materials.

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%
Chiral Purity	Contact for details
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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