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Sodium 5,5-Diethyl-1-Phenylbarbiturate CAS NO 59960-26-8


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CAS No.:59960-26-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Sodium 5,5-Diethyl-1-Phenylbarbiturate is the sodium salt of a phenyl-substituted barbituric acid derivative, offering enhanced solubility and stability for precise formulation. This compound serves as a critical pharmaceutical intermediate and reference standard in analytical chemistry and drug development. It is primarily required by manufacturers and research institutions in the pharmaceutical, life sciences, and fine chemical synthesis sectors.

Application

  • Pharmaceutical Intermediate: Key starting material or precursor in the synthesis of specialized barbiturate-based active pharmaceutical ingredients (APIs).
  • Analytical Reference Standard: Used for method development, calibration, and quality control in HPLC, GC, and other chromatographic analyses within pharmaceutical QC labs.
  • Biochemical Research: Employed in neuroscience and pharmacological studies investigating GABAA receptor modulation and sedative-hypnotic mechanisms.
  • Chemical Synthesis: Serves as a building block for the preparation of more complex organic molecules in medicinal chemistry and fine chemical production.
  • Veterinary Medicine: Potential use in the formulation of veterinary sedatives or anesthetics, subject to appropriate regulatory approvals.

Basic Information

Product Name Sodium 5,5-Diethyl-1-Phenylbarbiturate
CAS No. 59960-26-8
Molecular Formula C14H15N2NaO3
Molecular Weight 282.27 g/mol
Synonyms 5,5-Diethyl-1-phenylbarbituric Acid Sodium Salt; Sodium Phenobarbital Derivative; 1-Phenyl-5,5-diethylbarbituric Acid Sodium Salt; Sodium 5,5-Diethyl-1-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione; NSC 401443; Barbituric Acid, 5,5-Diethyl-1-phenyl-, Sodium Salt; Phenylethylbarbituric Acid Sodium Salt
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Quality Control

Our Sodium 5,5-Diethyl-1-Phenylbarbiturate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure high purity and consistency, meeting the stringent requirements for use as a pharmaceutical intermediate and reference standard. A comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥98.0%
Loss on Drying ≤2.0%
Heavy Metals ≤20 ppm
Residual Solvents Meets ICH guidelines
Related Substances (HPLC) Total impurities ≤2.0%

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

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