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80060-09-9
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Diafenthiuron
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POLO;PEGASUS;cga106630;iafenthiuron;DIAFENTHIURON;Pegasus (pesticide);Diafenthiuron [iso];Butylurea technical;C12177000 Diafenthiuron;Diafenthiuron in Methanol
CBNumber:
CB9742062
???:
C23H32N2OS
??? ??:
384.58
MOL ??:
80060-09-9.mol
MSDS ??:
SDS

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???
144.6-147.7°C
?? ?
448.8±55.0 °C(Predicted)
??
1.0367 (rough estimate)
???
1.5950 (estimate)
???
149 °C
?? ??
0-6°C
???
?????(?? ???), ???(?? ???)
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Solid
?? ?? (pKa)
12?+-.0.70(Predicted)
??
???? ?????
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Water: < 0.1 mg/mL (insoluble)
Merck
13,2988
BRN
8343025
CAS ??????
80060-09-9(CAS DataBase Reference)
EPA
Diafenthiuron (80060-09-9)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xn
?? ???? ?? 20
????? 22
????(UN No.) UN 2811
WGK ?? 2
RTECS ?? XN9100000
?? ?? 6.1(a)
???? II
HS ?? 29309090
?? LD50 in rats (mg/kg): 2068 orally; >2000 dermally; LC50 (14 hr) in rats: 558 mg/m3 by inhalation (Streibert, 1988)
???? ?? KE-05-0268
?????? ??? 97-1-15
?? ? ???? ????: ????; ???(??)????: ??????? ? ?? 25% ?? ??? ???
????(GHS): GHS hazard pictograms
?? ?: Warning
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?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H332 ???? ??? ?? ?? ?? ?? ?? 4 ?? GHS hazard pictograms P261, P271, P304+P340, P312
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P261 ??·?·??·???·??·...·????? ??? ????.
P271 ?? ?? ??? ? ?? ???? ?????.

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Diafenthiuron is a broad spectrum acaricide and insecticide, diafenthiuron is registered for use on cotton, soybeans, vegetables, fruit and ornamentals. It controls all post-hatch stages of mites, whiteflies and aphids. Its ability to control all sucking pests of cotton as well as mites, with no known toxicity to beneficial insects, is unique and very valuable in cotton integrated pest management (IPM) programs.

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Diafenthiuron is an insecticide.

Toxicology

Diafenthiuron has low toxicity to birds, mammals and beneficial insects, and is only slightly toxic to predatory mites. It is toxic to fish, but presents little hazard because it is rapidly degraded.

Mode of action

Diafenthiuron is a proinsecticide, which means that it must be converted to another compound – the drug – in order to be toxic. Activation of diafenthiuron to its carbodiimide drug occurs on the leaf surface, catalyzed by light, or in the insect, catalyzed by P450 monooxygenases. Diafenthiuron carbodiimide binds to the glutamate residue in the transmembrane F0 subunit of ATP synthase where protons from the intermembrane space dock to begin their journey across the inner mitochondrial membrane. Binding of diafenthiuron carbodiimide to this site blocks proton transport and ATP synthesis. Diafenthiuron was launched in 1991 and resistance has not yet been reported.

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