GV (nerve agent): Difference between revisions

GV (nerve agent)
Names
	IUPAC name 2-(Dimethylamino)ethyl N,N-dimethylphosphoramidofluoridate
Identifiers
CAS Number	141102-74-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	112656 ;
PubChem CID	132333;
CompTox Dashboard (EPA)	DTXSID30930987 ;
	InChI InChI=1S/C6H16FN2OP/c1-8(2)5-6-11(7,10)9(3)4/h5-6H2,1-4H3 Key: JJHAGEZAXYOCMC-UHFFFAOYSA-N ; InChI=1/C6H16FN2OP/c1-8(2)5-6-11(7,10)9(3)4/h5-6H2,1-4H3 Key: JJHAGEZAXYOCMC-UHFFFAOYAS;
	SMILES FP(=O)(N(C)C)CCN(C)C;
Properties
Chemical formula	C6H16FN2O2P
Molar mass	198.176 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Revision as of 10:20, 9 September 2013

GV (IUPAC name: 2-(Dimethylamino)ethyl N,N-dimethylphosphoramidofluoridate) is an organophosphate nerve agent. GV is a part of a new series of nerve agents with properties similar to both the "G-series" and "V-series". It is a potent acetylcholinesterase inhibitor with properties similar to other nerve agents, being a highly poisonous vapour. Treatment for poisoning with GV involves drugs such as atropine, benactyzine, obidoxime and HI-6.^[1]^[2]

References

^ Fusek J, Bajgar J (1994). "Treatment of intoxication with GV compound in laboratory rats". Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove. 37 (2): 57–62. PMID 7784799.
^ Kassa J, Bajgar J (1996). "Therapeutic efficacy of obidoxime or HI-6 with atropine against intoxication with some nerve agents in mice". Acta Medica (Hradec Kralove). 39 (1): 27–30. PMID 9106387.

External links

Harvey SP, Cheng TC (2002). "Identification, Purification, and Partial Characterization of the GV-Degrading Enzyme from ATCC # 29660 Alteromonas undina" (pdf). Aberdeen Proving Ground: Edgewood. Report ECBC-TR-229.
Bajgar J (1998). "Some Toxic Chemicals as Potential Chemical Warfare Agents - The Threat for the Future?". ASA Newsletter. 1998 (6).

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[1] Fusek J, Bajgar J (1994). "Treatment of intoxication with GV compound in laboratory rats". Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove. 37 (2): 57–62. PMID 7784799.

[2] Kassa J, Bajgar J (1996). "Therapeutic efficacy of obidoxime or HI-6 with atropine against intoxication with some nerve agents in mice". Acta Medica (Hradec Kralove). 39 (1): 27–30. PMID 9106387.

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 ==External links==
 {{Commons category|GV nerve agent}}
-*[http://stinet.dtic.mil/oai/oai?&verb=getRecord&metadataPrefix=html&identifier=ADA411415 Identification, Purification, and Partial Characterization of the GV-Degrading Enzyme from ATCC # 29660 Alteromonas Undina]
+*{{ cite web | author = Harvey SP, Cheng TC | title = Identification, Purification, and Partial Characterization of the GV-Degrading Enzyme from ATCC # 29660 ''Alteromonas undina'' | publisher = Edgewood | location = Aberdeen Proving Ground | year = 2002 | id = Report ECBC-TR-229 | url = http://www.dtic.mil/cgi-bin/GetTRDoc?Location=U2&doc=GetTRDoc.pdf&AD=ADA411415 | format = pdf }}
 *{{ cite journal | author = Bajgar J | title = Some Toxic Chemicals as Potential Chemical Warfare Agents - The Threat for the Future? | journal = ASA  Newsletter | year = 1998 | volume = 1998 | issue = 6 | url = http://www.asanltr.com/ASANews-98/chemistry.html }}

Revision as of 10:20, 9 September 2013

References

See also

External links