Description

1-(Isopropylamino)-3-(2,6-Xylidino)-2-Propanol is a high-purity chemical intermediate of significant importance in advanced pharmaceutical synthesis. This compound matters for its role as a key building block in the production of specialized β-adrenergic blocking agents and other active pharmaceutical ingredients (APIs). Pharmaceutical manufacturers, contract research organizations (CROs), and fine chemical suppliers need it to ensure the integrity and efficacy of their final drug products.

Application

• Pharmaceutical Intermediate: Primary use as a critical precursor in the synthesis of β-blocker APIs and related cardiovascular medications.
• Fine Chemical Synthesis: Serves as a versatile building block for creating complex molecules with specific stereochemistry in research and development.
• Active Pharmaceutical Ingredient (API) Manufacturing: Integral component in multi-step synthesis processes under Good Manufacturing Practice (GMP) conditions.
• Biochemical Research: Used in pharmacological studies to investigate adrenergic receptor mechanisms and develop new therapeutic agents.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Reference Standard: High-purity grades are utilized as analytical standards for quality control and regulatory compliance testing.

Basic Information

Product Name	1-(Isopropylamino)-3-(2,6-Xylidino)-2-Propanol
CAS No.	20013-95-0
Molecular Formula	C15H26N2O
Molecular Weight	250.38 g/mol
Synonyms	2-Propanol, 1-(isopropylamino)-3-(2,6-dimethylanilino)-; 1-(Isopropylamino)-3-(2,6-dimethylanilino)-2-propanol; 3-(2,6-Dimethylanilino)-1-(isopropylamino)-2-propanol; Xylidino Propanol Derivative; Isopropylamino Xylidino Propanol; N-Isopropyl-N'-(2,6-dimethylphenyl)-2-hydroxy-1,3-propanediamine; A potential precursor to tolamolol and related compounds.
EINECS	Contact for details

Quality Control

Our 1-(Isopropylamino)-3-(2,6-Xylidino)-2-Propanol is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the high standards required for pharmaceutical intermediates. Certificates of Analysis (COA) detailing all specifications are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, 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
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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