{"ATC Code":"N - Nervous system","Abbreviation":"","Aliases":["Barbitone","5,5-Diethylbarbituric acid","Ethylbarbital","Diemal","Diethylmalonylurea","DEBA","5,5-diethylpyrimidine-2,4,6(1H,3H,5H)-trione","200-331-2","Veronal","Malonal","Vesperal","Uronal","Diethylbarbitone","Dormonal","Hypnogene","Veroletten","Verolettin","Sedeval","Diethylbarbituric acid","Barbitonum","Diemalum","Barbitale","Barbitalum","Diethyl-barbituric acid","2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-diethyl-"],"CAS":"57-44-3","ChEBI":"CHEBI:31252","ChEMBL":"CHEMBL444","ChemicalClasses":["barbiturate"],"Chirality":"achiral","DEA no":2145,"EINECS":"200-331-2","EliminationHalfLife":"30.3 (± 3.2) hours","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"200-331-2","Formating":[],"HMDB ID":"HMDB0248870","HeavyAtomCount":13,"IUPACName":"5,5-diethyl-1,3-diazinane-2,4,6-trione","InChI":"InChI=1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)","InChIKey":"FTOAOBMCPZCFFF-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Substances that do not act as agonists or antagonists but do affect the GAMMA-AMINOBUTYRIC ACID receptor-ionophore complex. GABA-A receptors (RECEPTORS, GABA-A) appear to have at least three allosteric sites at which modulators act: a site at which BENZODIAZEPINES act by increasing the opening frequency of GAMMA-AMINOBUTYRIC ACID-activated chloride channels; a site at which BARBITURATES act to prolong the duration of channel opening; and a site at which some steroids may act. GENERAL ANESTHETICS probably act at least partly by potentiating GABAergic responses, but they are not included here. (See all compounds classified as GABA Modulators.)","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e3\u003c/sub\u003e","MolecularWeight":"184.19 g/mol","PubChemId":2294,"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Barbital","Name":"Barbital","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q412409","Name":"Barbital","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB01483","Name":"Barbital","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/2294","Name":"Barbital","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL444","Name":"Barbital","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:31252","Name":"Barbital","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=57-44-3","Name":"Barbital","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0248870","Name":"Barbital","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D01740","Name":"Barbital","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/5WZ53ENE2P","Name":"Barbital","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID5022643","Name":"Barbital","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 2294, Barbital. Accessed July 13, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/2294\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/2294\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Barbital. UNII: 5WZ53ENE2P. Global Substance Registration System. Accessed July 13, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/5WZ53ENE2P\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/5WZ53ENE2P\u003c/a\u003e","Anvisa. RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. March 31, 2023. Accessed July 13, 2025. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003c/a\u003e"],"SMILES":"CCC1(C(=O)NC(=O)NC1=O)CC","SaltData":[{"AcidCount":1,"AmineCount":1,"Formula":"[Na+]","Name":"sodium","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 82.269 75.823\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h83v76H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m33.801 1.009 5.214 14.32M39.015 15.329l-9.794 11.676M29.221 27.005l-13.204 7.628\" class=\"bond\"/\u003e\u003cg 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sodium","UNII":"275L5M93QS"},{"AcidCount":1,"AmineCount":1,"Formula":"[K+]","Name":"potassium","Structure":null,"Title":"Barbital potassium","UNII":"QZ6VB88G2Z"},{"AcidCount":1,"AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.346 75.823\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v76H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m33.801 1.009 5.214 14.32M39.015 15.329l-9.794 11.676M29.221 27.005l-13.204 7.628\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M16.017 36.041 5.485 29.96M17.236 33.929 6.704 27.848\"/\u003e\u003cpath 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2.904M42.415 46.023l.002-5.699\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg fill=\"#1ff01f\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M78.029 36.06q-.786 0-1.238.53-.453.524-.453 1.446 0 .911.417 1.447.423.53 1.268.53.322 0 .607-.054.292-.059.566-.143v.536q-.274.101-.566.149-.291.054-.696.054-.744 0-1.25-.31-.5-.31-.75-.875-.25-.572-.25-1.34 0-.744.268-1.309.273-.566.803-.881.53-.322 1.28-.322.78 0 1.351.286l-.244.524q-.226-.101-.506-.185-.273-.083-.607-.083m2.757 4.423h-.601v-5.215h.601zM75.122 40.483h-.619v-2.286h-2.512v2.286h-.614v-4.899h.614v2.071h2.512v-2.071h.619z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Barbital hydrochloride","UNII":"48Q3695ASR"}],"Salts":["sodium","potassium","hydrochloride"],"Scheduling":[{"gov":"Brazil","ref":["3"],"schedule":"B1 substance"},{"gov":"Canada","ref":[],"schedule":"Schedule IV substance"},{"act":"Controlled Substances Act (CSA)","gov":"United 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