Description

5-(Ethoxymethyl)-5-Ethylbarbituric Acid is a specialized barbiturate derivative, a key building block in advanced organic synthesis. This compound matters for its role as a critical intermediate in the development of pharmaceutical actives and fine chemicals, offering precise structural control. Industrial buyers in pharmaceutical R&D, agrochemical synthesis, and specialty chemical manufacturing need this high-purity intermediate to ensure the integrity and efficacy of their final products.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of novel barbiturate-based active pharmaceutical ingredients (APIs) and central nervous system (CNS) agents.
• Agrochemical Synthesis: Used in the research and development of specialized herbicides and pesticides, leveraging its heterocyclic core structure.
• Fine Chemical Manufacturing: Serves as a versatile building block for creating complex molecules in custom synthesis and contract manufacturing.
• Research & Development: Employed in academic and industrial laboratories for medicinal chemistry studies and the exploration of new therapeutic pathways.
• Chemical Reference Standard: Utilized as a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Product Name	5-(Ethoxymethyl)-5-Ethylbarbituric Acid
CAS No.	66941-27-3
Molecular Formula	C9H14N2O4
Molecular Weight	214.22 g/mol
Synonyms	5-Ethyl-5-(ethoxymethyl)barbituric acid; 5-(Ethoxymethyl)-5-ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 5-Ethyl-5-(ethoxymethyl)-1,3-diazinane-2,4,6-trione; NSC 163045; Barbituric acid, 5-ethyl-5-(ethoxymethyl)-; 5-Ethyl-5-(ethoxymethyl)pyrimidine-2,4,6(1H,3H,5H)-trione
EINECS	Contact for details

Quality Control

Our 5-(Ethoxymethyl)-5-Ethylbarbituric Acid is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing key parameters such as assay, identity, and impurity profiles. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your most critical synthesis stages.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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