Description

5-(2,3,4-Trimethoxyphenyl)-5-Oxovaleric Acid is a high-purity organic intermediate characterized by its distinct trimethoxyphenyl and oxovaleric acid functional groups. This compound is of significant commercial value for its role as a versatile building block in advanced organic synthesis, enabling the development of complex molecular architectures. It is primarily sought after by research institutions and manufacturers in the pharmaceutical and fine chemical sectors for the synthesis of active pharmaceutical ingredients (APIs) and other specialty chemicals.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of novel drug candidates and active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular pathways.
• Fine Chemical Synthesis: Serves as a crucial building block for constructing complex organic molecules used in agrochemicals, dyes, and specialty polymers.
• Research & Development: Utilized in academic and industrial R&D laboratories for method development, structure-activity relationship (SAR) studies, and exploring new chemical entities.
• Chemical Reference Standard: Employed as a high-purity analytical standard for quality control and regulatory compliance testing in manufacturing processes.

Basic Information

Product Name	5-(2,3,4-Trimethoxyphenyl)-5-Oxovaleric Acid
CAS No.	16093-16-6
Molecular Formula	C14H18O6
Molecular Weight	282.29 g/mol
Synonyms	5-Oxo-5-(2,3,4-trimethoxyphenyl)valeric acid; 4-(2,3,4-Trimethoxyphenyl)-4-oxobutanoic acid; δ-Oxo-2,3,4-trimethoxybenzenebutanoic acid; 5-(2,3,4-Trimethoxybenzoyl)valeric acid; 16093-16-6; 5-(2,3,4-Trimethoxyphenyl)-5-oxopentanoic acid; 4-Carboxy-1-(2,3,4-trimethoxyphenyl)-1-butanone
EINECS	Contact for details

Quality Control

Our 5-(2,3,4-Trimethoxyphenyl)-5-Oxovaleric 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 specified parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliable supply and traceability for critical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from strong oxidizing agents, strong bases, and sources of ignition. For long-term storage, consider inert atmosphere conditions to maintain optimal purity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 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.