Description

Oxolamine is a synthetic organic compound with significant utility in pharmaceutical research and development. This versatile chemical intermediate is valued for its role in the synthesis of active pharmaceutical ingredients (APIs) and other fine chemicals. It is primarily sought by manufacturers and R&D laboratories in the pharmaceutical, agrochemical, and life science sectors for process development and scale-up activities.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of various therapeutic agents and active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for the discovery and optimization of new drug candidates.
• Agrochemical Synthesis: Serves as a precursor in the manufacturing of certain crop protection agents and pesticides.
• Fine Chemical Production: Employed in the synthesis of complex, high-value specialty chemicals for diverse industrial applications.
• Biochemical Research: Utilized as a reagent or standard in biochemical assays and metabolic studies.

Basic Information

Product Name	Oxolamine
CAS No.	959-14-8
Molecular Formula	C14H21NO3
Molecular Weight	251.32 g/mol
Synonyms	Perebron; 2-(3,5-Dimethylphenoxymethyl)-2-imidazoline; 2-[(3,5-Dimethylphenoxy)methyl]-4,5-dihydro-1H-imidazole; Oxolamine citrate (salt form); Dimexoline; Imidazoline derivative; 959-14-8; 2-(3,5-Dimethylphenoxymethyl)-4,5-dihydroimidazole
EINECS	213-513-9

Quality Control

Our Oxolamine is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with key parameters such as assay, impurity profile, and residual solvents, supporting compliance with cGMP and other relevant regulatory guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
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.