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S-Thiopental CAS NO 20224-43-5
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CAS No.:20224-43-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
S-Thiopental is a thiobarbiturate derivative, a key chemical intermediate in pharmaceutical research and development. Its primary value lies in its role as a precursor for synthesizing specialized anesthetic and central nervous system (CNS) agents. This compound is essential for R&D laboratories and manufacturers in the pharmaceutical and fine chemical sectors focusing on neuropharmacology and anesthetic drug development.
Application
- Pharmaceutical Intermediate: Primary use as a building block for the synthesis of thiobarbiturate-based anesthetic agents.
- Research & Development: Critical material in medicinal chemistry for studying structure-activity relationships (SAR) of barbiturate analogs.
- Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
- Biochemical Studies: Used in preclinical research to investigate mechanisms of action related to GABAA receptor modulation.
- Fine Chemical Synthesis: Intermediate for creating more complex, specialized molecules in custom synthesis projects.
Basic Information
| Product Name | S-Thiopental |
| CAS No. | 20224-43-5 |
| Molecular Formula | C11H18N2O2S |
| Molecular Weight | 242.34 g/mol |
| Synonyms | Thiopental Impurity C; 5-Ethyl-5-(1-methylbutyl)-2-thiobarbituric Acid; Thiopental Related Compound C; Penthiobarbital; Thiopenal; NSC 76098; 2-Thiobarbituric acid, 5-ethyl-5-(1-methylbutyl)-; 5-Ethyl-5-(1-methylbutyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione |
| EINECS | Contact for details |
Quality Control
Our S-Thiopental is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical data supporting identity, purity, and impurity profiles. A Certificate of Analysis (COA) is supplied with each batch, detailing results from tests including HPLC assay, related substances, residual solvents, and identification. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates.
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). Due to its hygroscopic nature, the container must be kept tightly sealed to exclude moisture. Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥98.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% Any single impurity ≤0.5% |
| Loss on Drying | ≤1.0% |
| 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.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






