| BUTABARBITAL Basic information |
Product Name: | BUTABARBITAL | Synonyms: | 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-(1-methylpropyl)-;5-Ethyl-5-(1-methylpropyl)-2,4,6(1H,3H,5H)-pyrimidinetrione;BUTABARBITAL;5-ethyl-5-(1-methylpropyl)barbiturate;5-Ethyl-5-(1-methylpropyl)barbituric acid;5-ethyl-5-(1-methylpropyl)barbituricacid;5-Sec-butyl-5-ethyl-2,4,6(1H,3H,5H)-pyrimidinetrione;5-sec-Butyl-5-Ethylbarbituric acid | CAS: | 125-40-6 | MF: | C10H16N2O3 | MW: | 212.25 | EINECS: | 204-738-6 | Product Categories: | Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals | Mol File: | 125-40-6.mol | |
| BUTABARBITAL Chemical Properties |
Melting point | 166.5°C | Boiling point | 352.08°C (rough estimate) | density | 1.1718 (rough estimate) | refractive index | 1.4550 (estimate) | Fp | 9℃ | storage temp. | -20°C | solubility | DMSO (Slightly), Methanol (Slightly) | pka | 7.93±0.10(Predicted) | form | Solid | color | White | Water Solubility | 848.3mg/L(25 ºC) | CAS DataBase Reference | 125-40-6 | EPA Substance Registry System | 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-ethyl-5-(1-methylpropyl)- (125-40-6) |
| BUTABARBITAL Usage And Synthesis |
Description | Butabarbital (CRM) (Item No. 20088) is a certified reference material categorized as a barbiturate. It has a high abuse potential and increases risk of overdose morbidity and mortality in recreational drug users. Butabarbital is regulated as a Schedule III compound in the United States. Butabarbital (CRM) (Item No. 20088) is provided as a DEA exempt preparation. This product is intended for research and forensic applications. | Uses | Controlled substance (depressant). Sedative, hypnotic. | Uses | Butabarbital is also used as a soporific drug in various forms of insomnia and as a sedative. The most frequently used synonym is butizone. | Definition | ChEBI: Butabarbital is a member of barbiturates. | Brand name | Butabarb (Alpharma);
Butalan (Lannett); Buticaps (Medpointe); Butisol Sodium
(Medpointe); Sarisol (Halsey). | Synthesis | Butabarbital, 5-ethyl-5-isobutylbarbituric acid (4.1.11), is also synthesized
in an analogous manner by condensation of |á-ethyl-|á-isobutylmalonic ester with urea [9]. |
| BUTABARBITAL Preparation Products And Raw materials |
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