Description

3-(2,4-Dimethyl-6-Oxo-1,6-Dihydropyridin-3-Yl)Propanoic Acid (Saltdata: Free) is a high-purity, non-salt form organic intermediate with a defined pyridone core structure. This compound is valued for its role as a critical building block in advanced pharmaceutical synthesis and fine chemical research. It is primarily sought after by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and specialty chemical industries for constructing complex molecular architectures.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of active pharmaceutical ingredients (APIs), particularly those targeting neurological or metabolic pathways.
• Agrochemical Research: Used as a building block for developing novel herbicides, fungicides, or plant growth regulators.
• Ligand Synthesis: Serves as a starting material for creating complex ligands used in catalysis and metal-organic frameworks (MOFs).
• Fine Chemical Production: Employed in the manufacture of specialty dyes, pigments, and advanced materials.
• Academic & Contract Research: Essential for medicinal chemistry programs and structure-activity relationship (SAR) studies in academic and CRO settings.
• Bioconjugate Chemistry: Potential use in designing linkers for antibody-drug conjugates (ADCs) due to its carboxylic acid functionality.

Basic Information

Item	Details
Product Name	3-(2,4-Dimethyl-6-Oxo-1,6-Dihydropyridin-3-Yl)Propanoic Acid (Saltdata: Free)
CAS No.	1119453-13-2
Molecular Formula	C10H13NO3
Molecular Weight	195.22 g/mol
Synonyms	3-(2,4-Dimethyl-6-oxo-1,6-dihydropyridin-3-yl)propanoic acid; 3-(2,4-Dimethyl-6-oxo-1,4,5,6-tetrahydropyridin-3-yl)propanoic acid; 2,4-Dimethyl-3-(2-carboxyethyl)-6-pyridone; 6-Hydroxy-2,4-dimethyl-3-(2-carboxyethyl)pyridine; 1119453-13-2; Free acid form of related pyridone derivative.
EINECS	Contact for details

Quality Control

Our production of 3-(2,4-Dimethyl-6-Oxo-1,6-Dihydropyridin-3-Yl)Propanoic Acid adheres to stringent in-process controls and final release testing to ensure batch-to-batch consistency and high purity. We employ advanced analytical techniques including HPLC, GC, NMR, and MS for comprehensive characterization. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment. Our quality system supports compliance with cGMP and ISO standards for pharmaceutical intermediates.

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). Keep the container sealed to minimize exposure to atmospheric moisture. Store away from incompatible materials such as strong oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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