Weight | 184.195 g/mol |
---|---|
Formula | C8H12N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
barbital (57-44-3, 144-02-5)
Veronal · Barbitone · Medinal
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#595 in Neuroscience
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#3360 in Chemistry
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- CXCVIII.Universal buffer solutions and the dissociation constant of veronal (Journal of The Chemical Society (resumed), 1931)
- Three second chromosome-linked clustered Cyp6 genes show differential constitutive and barbital-induced expression in DDT-resistant and susceptible strains of Drosophila melanogaster (Gene, 1996)
- Stimulatory effect of barbital on urinary excretion of L-ascorbic acid and nonconjugated D-glucuronic acid. (Journal of Biological Chemistry, 1957)
- Effect of GABAergic drugs on motor impairment from ethanol, barbital and lorazepam in rat lines selected for differential sensitivity to ethanol (Pharmacology, Biochemistry and Behavior, 1989)
- Promoting effects of phenobarbital and barbital on development of thyroid tumors in rats treated with N-bis(2-hydroxypropyl)nitrosamine (Carcinogenesis, 1982)
- Delirium tremens: a double-blind comparison of diazepam and barbital treatment. (Acta Psychiatrica Scandinavica, 1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Veronal
- Barbitone
- Medinal
- Diethylmalonylurea
- Faes Brand of Barbital
- Diemal
- Ethylbarbital
- Dormileno
- Barbital Faes Brand
-
SMILESCCC1(C(=O)NC(=O)NC1=O)CC
-
InChIKeyFTOAOBMCPZCFFF-UHFFFAOYSA-N
- Pubchem - barbital
- Wikipedia - barbital
Barbital (or barbitone), marketed under the brand names Veronal for the pure acid and Medinal for the sodium salt, was the first commercially available barbiturate. It was used as a sleeping aid (hypnotic) from 1903 until the mid-1950s. The chemical names for barbital are diethylmalonyl urea or diethylbarbituric acid; hence, the sodium salt (known as medinal, a genericised trademark in the United Kingdom) is known also as sodium diethylbarbiturate.
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