Anodyne| Barbital | |
|---|---|
 |
| Salts [] | |
|---|---|
| Sodium barbital | |
| |
| Barbital potassium | |
| |
| Barbital hydrochloride | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C8H12N2O3[1] |
|---|---|
| Molecular mass | 184.19 g/mol[1] |
| Predicted LogP | 0.6[1] |
| Chirality | achiral[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 5,5-diethyl-1,3-diazinane-2,4,6-trione[1] |
| SMILES | CCC1(C(=O)NC(=O)NC1=O)CC[1] |
| 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)[1] |
| InChIKey | FTOAOBMCPZCFFF-UHFFFAOYSA-N[1] |
| Dosing |
|---|
Barbital
Barbital (also known as Barbitone, Veronal, 5,5-Diethylbarbituric acid, Ethylbarbital, Diemal, Diethylmalonylurea, Malonal, Vesperal, Uronal or Diethylbarbitone) is a substance of the barbiturate class.
Chemistry
Barbital is typically found in the form of its sodium, potassium and hydrochloride salts.
Stereochemistry
Barbital is a achiral mixture
Legal status
- Brazil: Barbital is a B1 substance.
- Canada: Barbital is a Schedule IV substance.
- United States: Barbital is a Schedule IV substance.
- Germany: Barbital is a Anlage III substance.