| | SECOBARBITAL Basic information |
| Product Name: | SECOBARBITAL | | Synonyms: | SECOBARBITAL;QUINALBARBITONE;2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(1-methylbutyl)-5-(2-propenyl)-;2,4,6(1H,3H,5H)-Pyrimidinitrione, 5-(1-methylbutyl)-5-(2-propenyl)-;5-Allyl-5-(1-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione;5-allyl-5-(1-methylbutyl)barbiturate;5-allyl-5-(1-methylbutyl)-barbituricaci;5-Allyl-5-(1-methylbutyl)malonylurea | | CAS: | 76-73-3 | | MF: | C12H18N2O3 | | MW: | 238.28 | | EINECS: | 200-982-2 | | Product Categories: | Amines;Heterocycles;BarbituratesAlphabetic;SA - SMForensic and Veterinary Standards;Intermediates & Fine Chemicals;Pharmaceuticals;Chemical Structure;Drugs of Abuse;Drugs&Metabolites;S;Solutions | | Mol File: | 76-73-3.mol |  |
| | SECOBARBITAL Chemical Properties |
| | SECOBARBITAL Usage And Synthesis |
| Description | Secobarbital (CRM) (Item No. 21707) is a certified reference material categorized as a barbiturate. It extends intoxication and increases withdrawal effects in patients with a family history of alcoholism. Secobarbital is regulated as a Schedule II compound in the United States. Secobarbital (CRM) (Item No. 21707) is provided as a DEA exempt preparation. This product is intended for research and forensic applications. | | Uses | Barbiturates are being widely used as antiepileptics, hypnotics, and anesthetics
Controlled substance. | | Definition | ChEBI: A member of the class of barbiturates that is barbituric acid in which the hydrogens at position 5 are substituted by prop-2-en-1-yl and pentan-2-yl groups. | | Brand name | Seconal(Lilly);Seconal sodium;Tuinal. | | World Health Organization (WHO) | Secobarbital is a short to intermediate-acting barbiturate which is
controlled under Schedule III of the 1971 Convention on Psychotropic Substances.
See WHO comment for barbiturates.
(Reference: (UNCPS3) United Nations Convention on Psychotropic Substances (III),
, , 1971) | | Purification Methods | It is purified by dissolving the sodium salt [309-43-3] in 10% HCl which precipitates the acid form that is extracted into Et2O. The extract is dried (Na2SO4) and evaporated. The residue is then purified by repeated crystallisation from CHCl3. [Buchet & Sandorfy J Phys Chem 88 3274 1984, Beilstein 24 III/IV 2013.] |
| | SECOBARBITAL Preparation Products And Raw materials |
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