Description

Sodium 1-(1-Cyclohexen-1-Yl)-5,5-Diethylbarbiturate is a specialized barbiturate derivative salt, valued for its role as a key synthetic intermediate and active pharmaceutical ingredient (API) precursor. This compound matters for its precise chemical structure, which is critical in the synthesis of more complex molecules requiring the barbiturate pharmacophore. It is primarily needed by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic research institutions focused on developing new therapeutic agents or studying central nervous system (CNS) activity.

Application

• Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of novel barbiturate-based active pharmaceutical ingredients (APIs) and potential therapeutic compounds.
• Chemical Research & Development: Used in academic and industrial R&D settings for studying structure-activity relationships (SAR) of barbiturates and developing new chemical entities.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and impurity profiling of related pharmaceutical products.
• Fine Chemical Synthesis: Acts as a specialized reagent in multi-step organic synthesis for introducing the barbiturate moiety into more complex molecular architectures.

Basic Information

Product Name	Sodium 1-(1-Cyclohexen-1-Yl)-5,5-Diethylbarbiturate
CAS No.	94201-51-1
Molecular Formula	C14H19N2NaO3
Molecular Weight	286.30 g/mol
Synonyms	Sodium Cyclobarbital; Cyclobarbital Sodium; 5,5-Diethyl-1-(1-cyclohexen-1-yl)barbituric Acid Sodium Salt; 1-Cyclohexen-1-yl-5,5-diethylbarbituric Acid Sodium Salt; NSC 757280; Sodium 5,5-Diethyl-1-(1-cyclohexenyl)barbiturate; Cyclobarbitone Sodium; Phanodorm Sodium
EINECS	Contact for details

Quality Control

Our Sodium 1-(1-Cyclohexen-1-Yl)-5,5-Diethylbarbiturate is produced under a strict quality management system. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with detailed results from techniques such as HPLC, NMR, and IR spectroscopy. Specifications are designed to meet the stringent requirements of pharmaceutical R&D and fine chemical synthesis.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (NMR)	Conforms to structure
Assay (HPLC)	≥98.0%
Water Content (KF)	≤2.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
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.