Description

(3-Azepan-2-Yl-Phenyl)-Dimethyl-Amine, Oxalic Acid is a high-purity organic salt compound, specifically the oxalic acid salt of a substituted amine derivative. This compound is valued for its role as a key intermediate in advanced pharmaceutical synthesis and organic chemical research. It is primarily required by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and fine chemical industries for the development of novel active ingredients and complex molecular architectures.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel drug candidates, particularly those targeting neurological or psychiatric disorders.
• Chemical Research & Development: Used as a standardized reagent in organic synthesis for exploring new reaction pathways and creating complex nitrogen-containing heterocycles.
• Agrochemical Synthesis: Acts as a precursor in the development of new pesticides and herbicides with specific biological activity.
• Ligand and Catalyst Development: Utilized in the preparation of specialized ligands for metal catalysis and asymmetric synthesis applications.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Product Name	(3-Azepan-2-Yl-Phenyl)-Dimethyl-Amine, Oxalic Acid
CAS No.	1177272-51-3
Molecular Formula	C15H22N2 • C2H2O4
Molecular Weight	Contact for details
Synonyms	N,N-Dimethyl-1-(3-(azepan-2-yl)phenyl)methanamine oxalate; 1-[3-(2-Azepanyl)phenyl]-N,N-dimethylmethanamine oxalic acid salt; (3-(Azepan-2-yl)phenyl)dimethylamine oxalate; 2-(3-((Dimethylamino)methyl)phenyl)azepane oxalate; N,N-Dimethyl-1-(3-(hexahydroazepin-2-yl)phenyl)methanamine oxalate
EINECS	Contact for details

Quality Control

Our (3-Azepan-2-Yl-Phenyl)-Dimethyl-Amine, Oxalic Acid is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all relevant specifications. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical research and development projects.

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). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to prevent degradation. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%; Any single impurity ≤ 0.5%

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