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GP
Names
IUPAC name
2-[fluoro(methyl)phosphoryl]oxy-1,1-dimethylcyclopentane
Other names
2,2-Dimethylcyclopentyl methylphosphonofluoridate
Identifiers
3D model ( JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C8H16FO2P/c1-8(2)6-4-5-7(8)11-12(3,9)10/h7H,4-6H2,1-3H3
    Key: WLHVXHBOEJKSJU-UHFFFAOYSA-N
  • CC1(CCCC1OP(=O)(C)F)C
Properties
C8H16FO2P
Molar mass 194.186 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

GP is an organophosphate nerve agent of the G-series, [1] with a relatively slow rate of hydrolysis, and thus high stability and persistence in the environment. [2]

References

  1. ^ Ellison DH (2008). Handbook of Chemical and Biological Warfare Agents (Second ed.). CRC Press. ISBN  978-0-849-31434-6.
  2. ^ Harvey SP, McMahon LR, Berg FJ (January 2020). "Hydrolysis and enzymatic degradation of Novichok nerve agents". Heliyon. 6 (1): e03153. Bibcode: 2020Heliy...603153H. doi: 10.1016/j.heliyon.2019.e03153. PMC  7002793. PMID  32042950.
Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from " https://en.wikipedia.org/?title=GP_(nerve_agent)&oldid=1220671706"
From Wikipedia, the free encyclopedia
GP
Names
IUPAC name
2-[fluoro(methyl)phosphoryl]oxy-1,1-dimethylcyclopentane
Other names
2,2-Dimethylcyclopentyl methylphosphonofluoridate
Identifiers
3D model ( JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C8H16FO2P/c1-8(2)6-4-5-7(8)11-12(3,9)10/h7H,4-6H2,1-3H3
    Key: WLHVXHBOEJKSJU-UHFFFAOYSA-N
  • CC1(CCCC1OP(=O)(C)F)C
Properties
C8H16FO2P
Molar mass 194.186 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

GP is an organophosphate nerve agent of the G-series, [1] with a relatively slow rate of hydrolysis, and thus high stability and persistence in the environment. [2]

References

  1. ^ Ellison DH (2008). Handbook of Chemical and Biological Warfare Agents (Second ed.). CRC Press. ISBN  978-0-849-31434-6.
  2. ^ Harvey SP, McMahon LR, Berg FJ (January 2020). "Hydrolysis and enzymatic degradation of Novichok nerve agents". Heliyon. 6 (1): e03153. Bibcode: 2020Heliy...603153H. doi: 10.1016/j.heliyon.2019.e03153. PMC  7002793. PMID  32042950.
Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from " https://en.wikipedia.org/?title=GP_(nerve_agent)&oldid=1220671706"

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