Description

5-(1-Cyclohexen-1-Yl)-5-Ethyl-1,3-Dimethyl-2,4,6(1H,3H,5H)-Pyrimidinetrione is a specialized barbiturate derivative with a complex cyclic structure, offering unique chemical functionality for advanced synthesis. This compound is valued for its role as a key synthetic intermediate in the development of active pharmaceutical ingredients (APIs) and fine chemicals. It is primarily sought by research and development teams, as well as production chemists, in the pharmaceutical, agrochemical, and advanced material sectors for creating novel molecular entities.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel barbiturate-based or central nervous system (CNS) active pharmaceutical ingredients.
• Agrochemical Research: Used in the development of new pesticidal or herbicidal agents, leveraging its heterocyclic core for biological activity.
• Fine Chemical Synthesis: Acts as a versatile precursor for creating complex organic molecules in academic and industrial research laboratories.
• Material Science: Potential monomer or additive in the research of specialty polymers with specific thermal or optical properties.
• Chemical Reference Standard: Supplied as a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Product Name	5-(1-Cyclohexen-1-Yl)-5-Ethyl-1,3-Dimethyl-2,4,6(1H,3H,5H)-Pyrimidinetrione
CAS No.	891-90-7
Molecular Formula	C₁₄H₂₀N₂O₃
Molecular Weight	264.32 g/mol
Synonyms	5-(1-Cyclohexenyl)-5-ethyl-1,3-dimethylbarbituric Acid; 5-Ethyl-5-(1-cyclohexen-1-yl)-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 1,3-Dimethyl-5-ethyl-5-(1-cyclohexenyl)barbituric Acid; Cyclobarbital Impurity; Cyclobarbital Related Compound A; NSC 523764; 5-Ethyl-1,3-dimethyl-5-(1-cyclohexenyl)-2,4,6-pyrimidinetrione
EINECS	Contact for details

Quality Control

Our 5-(1-Cyclohexen-1-Yl)-5-Ethyl-1,3-Dimethyl-2,4,6(1H,3H,5H)-Pyrimidinetrione is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and IR spectroscopy, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specifications and test results. Our quality commitment supports compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

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 heat, sparks, and open flame. The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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