Phosfolan: Difference between revisions

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	\| ImageSize = 200px		\| ImageSize = 200px
	\| IUPACName = Diethyl 1,3-dithiolan-2-ylidenephosphoramidate		\| IUPACName = Diethyl 1,3-dithiolan-2-ylidenephosphoramidate
	\| OtherNames = Cyclan		\| OtherNames = Cyclan; N-diethoxyphosphoryl-1,3-dithiolan-2-imine
	\|Section1={{Chembox Identifiers		\|Section1={{Chembox Identifiers
	\| CASNo =		\| CASNo = 947-02-4
			\| CASNo_Ref = {{Cascite\|changed\|CAS}}
			\| ChEBI = 82145
	\| PubChem = 13689		\| PubChem = 13689
	\| ChemSpiderID = 13098		\| ChemSpiderID = 13098
			\| EINECS = 213-423-2
			\| KEGG = C19011
			\| UNNumber = 2783
			\| UNII = CHJ98J84AY
	\| SMILES = O=P(OCC)(/N=C1\SCCS1)OCC		\| SMILES = O=P(OCC)(/N=C1\SCCS1)OCC
	\| InChI = 1/C7H14NO3PS2/c1-3-10-12(9,11-4-2)8-7-13-5-6-14-7/h3-6H2,1-2H3		\| InChI = 1/C7H14NO3PS2/c1-3-10-12(9,11-4-2)8-7-13-5-6-14-7/h3-6H2,1-2H3
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	\| FlashPt =		\| FlashPt =
	\| AutoignitionPt =		\| AutoignitionPt =
			\| GHSPictograms = {{GHS06}}
			\| GHSSignalWord = Danger
			\| HPhrases = {{H-phrases\|300\|310}}
			\| PPhrases = {{P-phrases\|262\|264\|270\|280\|301+310\|302+350\|310\|321\|322\|330\|361\|363\|405\|501}}
	}}		}}
	}}		}}

	'''Phosfolan''' (]: C<sub>7</sub>H<sub>14</sub>NO<sub>3</sub>PS<sub>2</sub>) is a ] used as an ].		'''Phosfolan''' (]: C<sub>7</sub>H<sub>14</sub>NO<sub>3</sub>PS<sub>2</sub>) is a ] used as an ].<ref>{{cite web \|title=phosfolan data sheet \|url=http://www.alanwood.net/pesticides/phosfolan.html \|website=www.alanwood.net}}</ref><ref>{{cite journal \|last1=Soliman \|first1=S.A. \|last2=El‐Sebae \|first2=A.H. \|last3=El‐Fiki \|first3=Sorya \|title=Occupational effect of phosfolan insecticide on spraymen during field exposure \|journal=Journal of Environmental Science and Health, Part B \|date=January 1979 \|volume=14 \|issue=1 \|pages=27–37 \|doi=10.1080/03601237909372112\|pmid=429759 }}</ref>

	==References==		==References==
	{{~~reflist~~}}		{{Reflist}}

			==External links==
			*{{Commonscatinline}}

	{{Insecticides}}		{{Insecticides}}
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	]		]
	]		]
	]		]

Latest revision as of 09:29, 9 May 2024

Phosfolan
Names

IUPAC name Diethyl 1,3-dithiolan-2-ylidenephosphoramidate
Other names Cyclan; N-diethoxyphosphoryl-1,3-dithiolan-2-imine
Identifiers
CAS Number	947-02-4
3D model (JSmol)	Interactive image
ChEBI	CHEBI:82145
ChemSpider	13098
ECHA InfoCard	100.012.203
EC Number	213-423-2
KEGG	C19011
PubChem CID	13689
UNII	CHJ98J84AY
UN number	2783
CompTox Dashboard (EPA)	DTXSID1042285
InChI InChI=1S/C7H14NO3PS2/c1-3-10-12(9,11-4-2)8-7-13-5-6-14-7/h3-6H2,1-2H3Key: ILBONRFSLATCRE-UHFFFAOYSA-N InChI=1/C7H14NO3PS2/c1-3-10-12(9,11-4-2)8-7-13-5-6-14-7/h3-6H2,1-2H3Key: ILBONRFSLATCRE-UHFFFAOYAJ
SMILES O=P(OCC)(/N=C1\SCCS1)OCC
Properties
Chemical formula	C₇H₁₄NO₃PS₂
Molar mass	255.29 g·mol
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H300, H310
Precautionary statements	P262, P264, P270, P280, P301+P310, P302+P350, P310, P321, P322, P330, P361, P363, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Phosfolan (chemical formula: C₇H₁₄NO₃PS₂) is a chemical compound used as an insecticide.

References

"phosfolan data sheet". www.alanwood.net.
Soliman, S.A.; El‐Sebae, A.H.; El‐Fiki, Sorya (January 1979). "Occupational effect of phosfolan insecticide on spraymen during field exposure". Journal of Environmental Science and Health, Part B. 14 (1): 27–37. doi:10.1080/03601237909372112. PMID 429759.

External links

Media related to Phosfolan at Wikimedia Commons

v t e Pest control: Insecticides
Carbamates	Aldicarb Aminocarb Bendiocarb Butocarboxim Carbaryl Carbofuran Carbosulfan m-Cumenyl methylcarbamate Ethienocarb Fenobucarb Isoprocarb Methomyl Metolcarb Oxamyl Promecarb Propoxur
Inorganic compounds	Aluminium phosphide Boric acid Chromated copper arsenate Copper(II) arsenate Copper(I) cyanide Cryolite Diatomaceous earth Lead hydrogen arsenate Paris Green Scheele's Green
Insect growth regulators	Benzoylureas (Bistrifluron, Diflubenzuron, Flufenoxuron, Lufenuron, Noviflumuron) Hydroprene Methoprene Pyriproxyfen
Neonicotinoids	Acetamiprid Clothianidin Dinotefuran Imidacloprid Imidaclothiz Nitenpyram Nithiazine Paichongding Thiacloprid Thiamethoxam
Organochlorides	Aldrin Beta-HCH Carbon tetrachloride Chlordane Cyclodiene 1,2-DCB 1,4-DCB 1,1-DCE 1,2-DCE DDD DDE DDT DFDT Dicofol Dieldrin Endosulfan Endrin Heptachlor Kepone Lindane Methoxychlor Mirex Tetradifon Toxaphene
Organophosphorus	Acephate Azamethiphos Azinphos-methyl Bensulide Chlorethoxyfos Chlorfenvinphos Chlorpyrifos Chlorpyrifos-methyl Coumaphos Demeton-S-methyl Diazinon Dichlorvos Dicrotophos Diisopropyl fluorophosphate Dimefox Dimethoate Dioxathion Disulfoton Ethion Ethoprop Fenamiphos Fenitrothion Fenthion Fosthiazate Isoxathion Malathion Methamidophos Methidathion Mevinphos Mipafox Monocrotophos Naled Omethoate Oxydemeton-methyl Parathion Parathion-methyl Phenthoate Phorate Phosalone Phosmet Phoxim Pirimiphos-methyl Quinalphos R-16661 Schradan Temefos Tebupirimfos Terbufos Tetrachlorvinphos Tribufos Trichlorfon
Pyrethroids	Acrinathrin Allethrins Bifenthrin Bioallethrin Cyfluthrin Cyhalothrin Cypermethrin Cyphenothrin Deltamethrin Empenthrin Esfenvalerate Etofenprox Fenpropathrin Fenvalerate Flumethrin Fluvalinate Imiprothrin Metofluthrin Permethrin Phenothrin Prallethrin Pyrethrin (I, II; chrysanthemic acid) Pyrethrum Resmethrin Silafluofen Tefluthrin Tetramethrin Tralomethrin Transfluthrin
Diamides	Chlorantraniliprole Cyantraniliprole Flubendiamide
Other chemicals	Afoxolaner Amitraz Azadirachtin Bensultap Buprofezin Cartap Chlordimeform Chlorfenapyr Cyromazine Fenazaquin Fenoxycarb Fipronil Fluralaner Hydramethylnon Indoxacarb Limonene Lotilaner (+milbemycin oxime) Pyridaben Pyriprole Sarolaner Adjuvants (Piperonyl butoxide, Sesamex) Spinosad Sulfluramid Tebufenozide Tebufenpyrad Veracevine Xanthone Metaflumizone Ryanodine Ryanodol
Metabolites	Oxon Malaoxon Paraoxon TCPy
Biopesticides	Bacillus thuringiensis Baculovirus Beauveria bassiana Beauveria brongniartii Isaria fumosorosea Metarhizium acridum Metarhizium anisopliae Nomuraea rileyi Lecanicillium lecanii Paenibacillus popilliae Purpureocillium lilacinum Spinosad