Description

(2-Oxoazepan-1-Yl)Acetic Acid is a high-purity organic compound featuring a caprolactam-derived structure with an acetic acid side chain, making it a versatile building block for advanced synthesis. This compound is valued for its role as a key intermediate in the development of specialized pharmaceuticals and fine chemicals. It is primarily sought by research institutions and industrial manufacturers in the pharmaceutical, agrochemical, and material science sectors for creating novel active ingredients and functional molecules.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of novel active pharmaceutical ingredients (APIs), particularly those targeting neurological and metabolic disorders.
• Protease Inhibitor Synthesis: Serves as a core scaffold for developing inhibitors of enzymes like proteases, which are relevant in therapeutic and research applications.
• Agrochemical Research: Used in the research and development of new generation pesticides and herbicides with improved efficacy and selectivity.
• Peptidomimetic Chemistry: Acts as a constrained building block for designing peptidomimetics, which are stable analogs of peptides used in drug discovery.
• Polymer Modification: Employed in the synthesis of specialty polymers and coatings to introduce specific functional groups that alter material properties.
• Chemical Biology Probes: Utilized in the creation of molecular probes for studying biological pathways and protein functions in academic and industrial research.

Basic Information

Product Name	(2-Oxoazepan-1-Yl)Acetic Acid
CAS No.	35048-56-7
Molecular Formula	C8H13NO3
Molecular Weight	171.19 g/mol
Synonyms	1-(Carboxymethyl)azepan-2-one; 2-Oxo-1-azepaneacetic Acid; N-(Carboxymethyl)caprolactam; 1-Azepanecarboxylic Acid, 2-oxo-; 2-Oxoazepane-1-acetic Acid; Caprolactam-N-acetic Acid; (2-Oxo-1-azepanyl)acetic Acid; N-Acetic Acid Caprolactam
EINECS	Contact for details

Quality Control

Our (2-Oxoazepan-1-Yl)Acetic Acid is manufactured under strict quality management systems. Every 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 critical parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your most demanding synthesis workflows.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). The product may be hygroscopic; keep the container tightly sealed in a dry environment to prevent moisture absorption. Keep away from strong oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals (as Pb)	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%

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