Description

5-Allyl-5-(β-Hydroxypropyl)-n-Phenylbarbituric Acid is a specialized barbiturate derivative, a key intermediate in the synthesis of complex pharmaceutical compounds. Its molecular structure, featuring both allyl and hydroxypropyl functional groups, provides a versatile scaffold for medicinal chemistry research and development. This compound is primarily utilized by R&D chemists and manufacturers in the pharmaceutical and fine chemical industries for creating new therapeutic agents, particularly in the central nervous system (CNS) drug category.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel barbiturate-based active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Serves as a versatile scaffold for structure-activity relationship (SAR) studies in drug discovery programs.
• CNS Drug Development: Used in the research and production of potential sedative, hypnotic, or anticonvulsant agents.
• Fine Chemical Synthesis: Employed as a precursor for the preparation of more complex, functionalized organic molecules.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control in pharmaceutical labs.

Basic Information

Product Name	5-Allyl-5-(β-Hydroxypropyl)-n-Phenylbarbituric Acid
CAS No.	14305-83-0
Molecular Formula	C16H18N2O4
Molecular Weight	302.33 g/mol
Synonyms	5-Allyl-5-(3-hydroxypropyl)-1-phenylbarbituric acid; 5-Allyl-5-(3-hydroxypropyl)-1-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 1-Phenyl-5-allyl-5-(3-hydroxypropyl)barbituric acid; 5-Allyl-5-(β-hydroxypropyl)-1-phenylbarbituric acid; 5-Allyl-5-(3-hydroxypropyl)-1-phenylpyrimidine-2,4,6(1H,3H,5H)-trione; 5-Allyl-5-(3-hydroxypropyl)-n-phenylbarbituric acid; Allylhydroxypropylphenylbarbituric Acid; Contact for additional trade names.
EINECS	Contact for details

Quality Control

Our 5-Allyl-5-(β-Hydroxypropyl)-n-Phenylbarbituric Acid is produced under strict quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and residual solvent analysis, to ensure it meets the stringent requirements for pharmaceutical intermediate applications. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider an inert atmosphere to maintain product integrity.

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%
Heavy Metals	≤20 ppm

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