Description

(S)-1-(Isopropylamino)-3-(4-(2-Methoxyethyl)Phenoxy)Propan-2-Ol is a high-purity chiral organic compound of significant interest in advanced pharmaceutical synthesis. Its core value lies in its role as a key chiral intermediate or building block for the development of enantiomerically pure active pharmaceutical ingredients (APIs). This product is essential for research institutions and manufacturers in the pharmaceutical and fine chemical industries who require high-quality, optically pure intermediates for drug discovery and process development.

Application

• Pharmaceutical Intermediate: A critical chiral building block for the synthesis of enantiomerically pure β-blockers and other cardiovascular agents.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in the research and production of specific, optically active drug molecules targeting adrenergic receptors.
• Biochemical Research: Serves as a standard or reagent in pharmacological studies investigating receptor-ligand interactions and stereoselectivity.
• Process Chemistry Development: Employed in the development and optimization of asymmetric synthesis routes within fine chemical manufacturing.
• Reference Standard: Used as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	(S)-1-(Isopropylamino)-3-(4-(2-Methoxyethyl)Phenoxy)Propan-2-Ol
CAS No.	114218-35-8
Molecular Formula	C15H25NO3
Molecular Weight	267.36 g/mol
Synonyms	(S)-1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]propan-2-ol; (S)-1-Isopropylamino-3-(4-(2-methoxyethyl)phenoxy)-2-propanol; (S)-Bisoprolol Intermediate; (S)-Bisoprolol Related Compound; (S)-1-[(1-Methylethyl)amino]-3-[4-(2-methoxyethyl)phenoxy]-2-propanol; (S)-Bisoprolol Impurity; (S)-Bisoprolol EP Impurity C; (S)-Bisoprolol USP RS
EINECS	Contact for details

Quality Control

Our (S)-1-(Isopropylamino)-3-(4-(2-Methoxyethyl)Phenoxy)Propan-2-Ol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chiral purity verification by HPLC, to ensure compliance with stringent specifications for pharmaceutical intermediates. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are 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 after opening to prevent moisture absorption, which may affect product stability and performance.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Chiral Purity (HPLC)	≥ 99.0% (S-enantiomer)
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 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.