Description

5-Allyl-5-(Butylthiomethyl)-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione is a specialized organosulfur derivative of barbituric acid, featuring a unique allyl and butylthiomethyl substitution pattern. This compound is valued for its role as a key synthetic intermediate and building block in advanced organic synthesis, particularly for creating complex heterocyclic systems. It is primarily utilized by research institutions and industrial R&D departments in the pharmaceutical and agrochemical sectors for developing novel active ingredients.

Application

• Pharmaceutical Intermediate: Serves as a crucial precursor in the synthesis of novel barbiturate analogs and other central nervous system (CNS) active compounds.
• Agrochemical Research: Used as a building block for developing new herbicides, fungicides, and plant growth regulators with specific thiomethyl functionalities.
• Organic Synthesis Reagent: Acts as a versatile reagent in nucleophilic substitution and cyclization reactions to construct complex pyrimidine-based scaffolds.
• Chemical Research: Employed in academic and industrial laboratories for studying structure-activity relationships (SAR) and reaction mechanisms involving sulfur-containing heterocycles.
• Material Science Precursor: Investigated for the development of specialty polymers and ligands for metal-organic frameworks (MOFs) due to its multiple functional groups.

Basic Information

Product Name	5-Allyl-5-(Butylthiomethyl)-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione
CAS No.	66941-59-1
Molecular Formula	C12H17N2NaO3S
Molecular Weight	292.33 g/mol
Synonyms	5-Allyl-5-(butylthiomethyl)barbituric acid sodium salt; Sodium 5-allyl-5-(butylthiomethyl)barbiturate; 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-allyl-5-[(butylthio)methyl]-, sodium salt; 5-Allyl-5-(butylthiomethyl)-2,4,6-pyrimidinetrione sodium derivative; Allylbutylthiomethylbarbituric Acid Sodium Salt
EINECS	Contact for details

Quality Control

Our production of 5-Allyl-5-(Butylthiomethyl)-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione adheres to stringent quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure consistency and compliance with research-grade specifications. A detailed Certificate of Analysis (COA) is provided with every shipment, guaranteeing traceability and meeting the exacting standards required for synthetic and R&D 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). The product is hygroscopic (moisture-sensitive); keep the container tightly sealed under an inert atmosphere such as nitrogen or argon to prevent degradation. Keep away from strong acids and oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%

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