| Weight | 212.249 g/mol |
|---|---|
| Formula | C10H16N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Butethal (77-28-1)
butobarbitone · Soneryl · butobarbital
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- Influence of sodium dodedecylsulphate and of inorganic electrolytes on the micellar solubilization of butobarbitone in aqueous polyoxyethylene lauryl ether solutions at 293.15 k (Colloids and Surfaces, 1985)
- Mass spectrometric determination of butobarbitone and its metabolites in man (Journal of Mass Spectrometry, 1974)
- The actions of amylobarbitone sodium, butobarbitone and quinalbarbitone sodium upon insomnia and nocturnal restlessness compared in psychiatric patients. (British journal of pharmacology and chemotherapy, 1961)
- The distribution of amylobarbitone, butobarbitone, pentobarbitone and quinalbarbitone and the hydroxylated metabolites in man. (Journal of Pharmacy and Pharmacology, 1979)
- Butobarbitone metabolism in man: identification of 3-ketobutobarbitone (Journal of Pharmacy and Pharmacology, 1974)
- Enzyme induction effects in the human metabolism of butobarbitone (European Journal of Drug Metabolism and Pharmacokinetics, 1976)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - butobarbitone
- Soneryl
- butobarbital
- butethal, monosodium salt
- 5-butyl-5-ethylbarbituric acid
- butobarbital, sodium salt
-
SMILESCCCCC1(C(=O)NC(=O)NC1=O)CC
-
InChIKeySTDBAQMTJLUMFW-UHFFFAOYSA-N
- Pubchem - Butethal
- Wikipedia - butethal
Butobarbital, also called butobarbitone or butethal, Soneryl, and Neonal, is a hypnotic drug which is a barbiturate derivative. It was developed by Poulenc Brothers (now part of Rhne Poulenc) in 1921.
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