Chlordimeform
Names | |
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IUPAC name N′-(4-chloro-2-methylphenyl)-N,N-dimethylmethanimidamide | |
Other names Chlorphenamidine; Chlorfenamidine; Fundal; Galecron | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChemSpider |
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ECHA InfoCard | 100.025.637 |
KEGG |
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PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C10H13ClN2 |
Molar mass | 196.68 g·mol−1 |
Appearance | White crystalline solid |
Melting point | 32 °C (90 °F; 305 K) (225-227 °C, hydrochloride) |
Solubility in water | 250 mg/L |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Chlordimeform is an acaricide (pesticide) active mainly against motile forms of mites and ticks and against eggs and early instars of some Lepidoptera insects.[1] After the International Agency for Research on Cancer reported sufficient evidence that its major metabolite, 4-chloro-o-toluidine, was a carcinogen, its use has ceased and its registration has been withdrawn in most countries.[1]
References
- ^ a b c Chlordimeform, International Program on Chemical Safety, World Health Organization
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- Aluminium phosphide
- Boric acid
- Chromated copper arsenate
- Copper(II) arsenate
- Copper(I) cyanide
- Cryolite
- Diatomaceous earth
- Lead hydrogen arsenate
- Paris Green
- Scheele's Green
- Acephate
- Azamethiphos
- Azinphos-methyl
- Bensulide
- Chlorethoxyfos
- Chlorfenvinphos
- Chlorpyrifos
- Chlorpyrifos-methyl
- Coumaphos
- Demeton-S-methyl
- Diazinon
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- Diisopropyl fluorophosphate
- Dimefox
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- Disulfoton
- Ethion
- Ethoprop
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- Mipafox
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- Naled
- Omethoate
- Oxydemeton-methyl
- Parathion
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- Phenthoate
- Phorate
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- Quinalphos
- R-16661
- Schradan
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- Fluralaner
- Hydramethylnon
- Indoxacarb
- Limonene
- Lotilaner (+milbemycin oxime)
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- Pyriprole
- Sarolaner
- Adjuvants (Piperonyl butoxide, Sesamex)
- Spinosad
- Sulfluramid
- Tebufenozide
- Tebufenpyrad
- Veracevine
- Xanthone
- Metaflumizone
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