Talbutal
| Talbutal | |
|---|---|
 | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 224.26 g/mol [1] |
| Appearance | CRYSTALS FROM WATER OR DIL ALCOHOL [1] |
| Odor | MAY HAVE SLIGHT ODOR OF CARAMEL [1] |
| Taste | SLIGHTLY BITTER TASTE [1] |
| Melting point | 108-110 °C [1] |
| Solubility | PRACTICALLY INSOL IN WATER & PETROLEUM ETHER SOL IN ALCOHOL, CHLOROFORM, ETHER, ACETONE, GLACIAL ACETIC ACID, FIXED ALKALI HYDROXIDE SOLN [1] |
| Predicted LogP | 1.4 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C11H16N2O3 [1] |
| IUPAC name | 5-butan-2-yl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione [1] |
| SMILES | CCC(C)C1(C(=O)NC(=O)NC1=O)CC=C [1] |
| InChI | InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16) [1] |
| InChIKey | BJVVMKUXKQHWJK-UHFFFAOYSA-N [1] |
Talbutal (also known as Talbutal, Lotusate, Profundol, 5-Allyl-5-sec-butylbarbituric acid, 115-44-6, Talbutale, Talbutalum, sec-Butyl allyl barbituric acid, WIN 5095 or Barbituric acid, 5-allyl-5-sec-butyl-) is a
Chemistry
Stereochemistry []
Talbutal is a racemic mixture of the enantiomers.
Pharmacology
ATC Classification
In the nervous system (N) talbutal acts as a barbiturates, plain (N05CA), hypnotics and sedative (N05C), psycholeptic (N05) and talbutal (N05CA07).[1]Metabolism
Subjective effects []
Legal status []
- Canada: Talbutal is a Schedule IV substance.
- United States: Talbutal is a Schedule I under the "Controlled Substances Act (CSA)".
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 8275, Talbutal. Accessed February 17, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/8275
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Talbutal. UNII: 4YIR8202AX. Global Substance Registration System. Accessed February 17, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4YIR8202AX