Description

5-Allyl-5-[1-(Allylthio)Ethyl]-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione is a specialized sodium salt derivative of a barbiturate analog, valued for its unique chemical structure that serves as a versatile synthetic intermediate. This compound is critical for researchers and manufacturers requiring precise building blocks for the development of novel pharmaceuticals and advanced organic materials. It is primarily sought after by the pharmaceutical R&D sector for creating potential active pharmaceutical ingredients (APIs) and by fine chemical producers for custom synthesis projects.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel barbiturate-derived compounds and other heterocyclic active pharmaceutical ingredients (APIs).
• Organic Synthesis Research: Versatile precursor for constructing complex molecular architectures in academic and industrial research laboratories.
• Agrochemical Development: Potential intermediate in the research and development of new crop protection agents and herbicides.
• Material Science: Used in the synthesis of specialty polymers and organic electronic materials requiring specific heterocyclic components.
• Chemical Biology Probes: Serves as a scaffold for developing molecular probes and diagnostic agents due to its modifiable functional groups.

Basic Information

Product Name	5-Allyl-5-[1-(Allylthio)Ethyl]-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione
CAS No.	66941-48-8
Molecular Formula	C12H15N2NaO3S
Molecular Weight	290.31 g/mol
Synonyms	Sodium 5-Allyl-5-[1-(allylthio)ethyl]-2,4,6-trioxo-1,3-diazinane-2-olate; 2-Sodiooxy-5-allyl-5-[1-(allylthio)ethyl]pyrimidine-4,6(1H,5H)-dione; 5-Allyl-5-(1-allylsulfanylethyl)-2-sodiooxypyrimidine-4,6-dione; Sodium 5-allyl-5-(1-allylsulfanylethyl)barbiturate; Allylthiobarbituric acid sodium salt derivative; Barbiturate sodium salt intermediate; CAS 66941-48-8
EINECS	Contact for details

Quality Control

Our 5-Allyl-5-[1-(Allylthio)Ethyl]-2-Sodiooxy-4,6(1H,5H)-Pyrimidinedione is produced under strict quality management protocols to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing key parameters such as identity, purity, and impurity profiles. We adhere to relevant cGMP guidelines for the production of pharmaceutical intermediates, and specifications can be tailored to meet specific project requirements.

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). The container should be kept tightly sealed in a dry environment to minimize exposure to moisture and air.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 95.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm

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