Description

Deacetylmoxisylyte is a high-purity pharmaceutical intermediate and fine chemical. This compound is valued for its role as a key building block in the synthesis of more complex active pharmaceutical ingredients (APIs). It is primarily required by manufacturers in the pharmaceutical, biotechnology, and advanced chemical research sectors for developing new therapeutic agents and conducting process optimization.

Application

• Pharmaceutical Intermediate: A critical precursor in the multi-step synthesis of specific vasodilator and adrenergic antagonist APIs.
• Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and the discovery of novel bioactive molecules.
• Process Chemistry: Serves as a standard or reference material for analytical method development and validation in API manufacturing.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	Deacetylmoxisylyte
CAS No.	35231-36-8
Molecular Formula	C11H15NO3
Molecular Weight	209.24 g/mol
Synonyms	2,5-Dimethoxyphenethylamine, N-Acetyl Derivative; 4-[2-(Dimethylamino)ethoxy]-2-methoxyphenyl acetate; Moxisylyte Impurity; Moxisylyte Related Compound A; Thymoxamine Impurity; 1-(4-Acetoxy-2-methoxy-5-methylphenyl)-2-(dimethylamino)ethanol (Deacetylated Form); Contact for IUPAC name.
EINECS	Contact for details

Quality Control

Our Deacetylmoxisylyte is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the high standards required for pharmaceutical intermediate applications. Certificates of Analysis (COA) with detailed chromatographic data 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 controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

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