Vinyl bit

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Structural formula
Structural formula of vinylbital
Structural formula without stereochemistry
General
Non-proprietary name Vinyl bit
other names
  • (±) -5-ethenyl-5- (1-methylbutyl) - (1 H , 3 H , 5 H ) -pyrimidine-2,4,6-trione
  • (±) -5- (1-methylbutyl) -5-vinylbarbituric acid
  • ( RS ) -5-ethenyl-5- (pentan-2-yl) pyrimidin-2,4,6-trione ( IUPAC )
  • Butyl vinal
  • Vinyl bitones
  • Vinilbital
  • JD 96
Molecular formula C 11 H 16 N 2 O 3
Brief description

crystalline powder

External identifiers / databases
CAS number
  • 2430-49-1
  • 5767-33-9 (-) - isomer
EC number 219-395-8
ECHA InfoCard 100.017.633
PubChem 72135
Wikidata Q410157
Drug information
ATC code

N05 CA08

Drug class

barbiturate

Mechanism of action

GABA A receptor agonist

properties
Molar mass 224.26 g mol −1
Physical state

firmly

Melting point

90-91.5 ° C

pK s value

7.89

safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Vinylbital is a medium-acting sedative and hypnotic from the group of barbiturates . The active ingredient was patented for BASF in 1960 ; currently (2013) there are no preparations with vinylbital on the market anywhere in the world. An isomer to vinyl bit is the structurally very similar vin bar bit .

Legal status

In the Federal Republic of Germany, vinylbital is a marketable narcotic, but not a prescription drug, because it is listed in Appendix 2 BtMG . Handling without permission is generally a criminal offense. Further information can be found in the main article Narcotics Law in Germany .

Internationally, Vinylbital falls under the Convention on Psychotropic Substances .

Individual evidence

  1. a b c d Entry on Vinylbital. In: Römpp Online . Georg Thieme Verlag, accessed on November 11, 2014.
  2. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  3. ^ BtMG accessed on January 30, 2010 .