Description

5-Butyl-5-(1-Ethylpropyl)-2,4,6(1H,3H,5H)-Pyrimidinetrione is a specialized barbiturate derivative, a class of compounds known for their significant role in medicinal chemistry and organic synthesis. This high-purity intermediate is critical for research and development in the pharmaceutical sector, where precise molecular structure and consistent quality are paramount. It serves as a key building block for scientists and manufacturers developing novel therapeutic agents, particularly in central nervous system (CNS) research.

Application

• Pharmaceutical Intermediate: A crucial precursor in the synthesis of active pharmaceutical ingredients (APIs) with barbiturate or related heterocyclic structures.
• Medicinal Chemistry Research: Used as a scaffold or building block in drug discovery programs, especially for targeting neurological pathways.
• Reference Standard: Serves as an analytical standard for quality control and method development in pharmaceutical laboratories.
• Chemical Synthesis: Employed in advanced organic synthesis to introduce complex pyrimidinetrione moieties into target molecules.
• Biochemical Research: Utilized in studies investigating the interaction of barbiturate-like compounds with biological systems.

Basic Information

Product Name	5-Butyl-5-(1-Ethylpropyl)-2,4,6(1H,3H,5H)-Pyrimidinetrione
CAS No.	67050-29-7
Molecular Formula	C₁₃H₂₂N₂O₃
Molecular Weight	254.33 g/mol
Synonyms	5-Butyl-5-(1-ethylpropyl)barbituric acid; 5-Butyl-5-(1-ethylpropyl)-2,4,6-trioxohexahydropyrimidine; 5-Butyl-5-(1-ethylpropyl)pyrimidine-2,4,6(1H,3H,5H)-trione; 5-(1-Ethylpropyl)-5-butylbarbituric acid; Barbituric acid, 5-butyl-5-(1-ethylpropyl)-; Butalbital Impurity/Intermediate
EINECS	Contact for details

Quality Control

Our 5-Butyl-5-(1-Ethylpropyl)-2,4,6(1H,3H,5H)-Pyrimidinetrione 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 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, well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials. For long-term storage, consider an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
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.