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TBPO

From Wikipedia, the free encyclopedia
TBPO[1]
Names
Preferred IUPAC name
4-tert-Butyl-2,6,7-trioxa-1λ5-phosphabicyclo[2.2.2]octan-1-one
Other names
t-Butyl-bicyclophosphate
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C8H15O4P/c1-7(2,3)8-4-10-13(9,11-5-8)12-6-8/h4-6H2,1-3H3
    Key: CNBZOKKOTFTYLW-UHFFFAOYSA-N
  • CC(C)(C)C12COP(=O)(OC1)OC2
Properties
C8H15O4P
Molar mass206.178 g·mol−1
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Extremely toxic
Lethal dose or concentration (LD, LC):
36 μg/kg (mice)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

TBPO is an extremely toxicbicyclic phosphateconvulsant andGABA receptor antagonist. It is the most toxicbicyclic phosphate known, with anLD50 of 36 μg/kg in mice.[2]

Some sources claim that TBPO is as toxic asVX.[3]

Synthesis

[edit]

The synthesis is equivalent to the synthesis ofIPTBO while the triol is produced by thecondensation between3,3-dimethylbutyraldehyde andformaldehyde analogous to the synthesis oftrimethylolpropane.

See also

[edit]

References

[edit]
  1. ^Zhao, C.; Hwang, S. H.; Buchholz, B. A.; Carpenter, T. S.; Lightstone, F. C.; Yang, J.; Hammock, B. D.; Casida, J. E. (27 May 2014)."GABAA receptor target of tetramethylenedisulfotetramine".Proceedings of the National Academy of Sciences.111 (23):8607–8612.Bibcode:2014PNAS..111.8607Z.doi:10.1073/pnas.1407379111.PMC 4060666.PMID 24912155.
  2. ^Milbrath, Dean S.; Engel, Judith L.; Verkade, John G.; Casida, John E. (February 1979). "Structure-toxicity relationships of 1-substituted-4-alkyl-2,6,7-trioxabicyclo[2.2.2.]octanes".Toxicology and Applied Pharmacology.47 (2):287–293.Bibcode:1979ToxAP..47..287M.doi:10.1016/0041-008x(79)90323-5.PMID 452023.
  3. ^Gupta RC (2015).Handbook of toxicology of chemical warfare agents (2nd ed.). Amsterdam: Elsevier/Academic Press. pp. 228–229.ISBN 9780128004944.OCLC 433545336.
GABA receptor antagonists
GABA synthesis inhibitors
Glycine receptor antagonists
Glutamate receptor agonists
Convulsantbarbiturates
Other
Animal toxins
Bacterial
Cyanotoxins
Plant toxins
Mycotoxins
Pesticides
Nerve agents
Bicyclic phosphates
Cholinergic neurotoxins
Psychoactive drugs
Other
Ionotropic
GABAATooltip γ-Aminobutyric acid A receptor
GABAATooltip γ-Aminobutyric acid A-rho receptor
Metabotropic
GABABTooltip γ-Aminobutyric acid B receptor
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