?????
|
|
????? ??
- ???
- <10 °C
- ?? ?
- 187-190 °C(Press: 0.2 Torr)
- ??
- 1.25 g/cm3(Temp: 25 °C)
- ???
- 1×10-6pa 20°C
- ???
- 2 °C
- ?? ??
- 2-8°C
- ???
- ????? (?? ???), DMSO (?? ???)
- ???
- 0.004mg l-1(20°C)
- ??? ??
- ??
- ??? ??
- ??? ??
- ??
- ???? ?????
- Henry's Law Constant
- 7.0×10-1 mol/(m3Pa) at 25℃, HSDB (2015)
- InChI
- InChI=1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3
- InChIKey
- ZXQYGBMAQZUVMI-UHFFFAOYSA-N
- SMILES
- C1(C(OC(C#N)C2=CC=CC(OC3=CC=CC=C3)=C2)=O)C(C=C(Cl)C(F)(F)F)C1(C)C
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | F,Xn | ||
|---|---|---|---|
| ?? ???? ?? | 11-20/21/22-36-52/53 | ||
| ????? | 26-36/37-61-16 | ||
| ????(UN No.) | 2902 | ||
| WGK ?? | 2 | ||
| ?? ?? | 6.1(b) | ||
| ???? | III | ||
| ???? ??? | 6.1A - Combustible acute toxic Cat. 1 and 2 very toxic hazardous materials |
||
| Hazard Classifications | Acute Tox. 1 Inhalation Acute Tox. 3 Oral Aquatic Acute 1 Aquatic Chronic 1 Eye Irrit. 2 Skin Irrit. 2 Skin Sens. 1B |
||
| ?? ?? ??? | 68085-85-8(Hazardous Substances Data) | ||
| ???? ?? | KE-05934 | ||
| ?????? ??? | 97-1-153 | ||
| ?? ? ???? | ????: ????; ???(??)????: ?????? ? ?? 1.0% ?? ??? ??? |
| ????(GHS): |
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| ?? ?: | Danger | |||||||||||||||||||||||||||||||||||||||||||||||||
| ??·?? ??: |
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| ??????: |
|
????? C??? ??, ??, ??
??
Cyhalothrin is used mainly for ectoparasite control on animals. Lambda-cyhalothrin has public health use and is also used for the control of a variety of insect pests in potatoes (Colorado beetle), cereals, hops, vegetables, cotton and other crops.??
ChEBI: A carboxylic ester obtained by formal condensation between 3-(2-chloro-3,3,3-trifluoroprop-1-en-1-yl)-2,2-dimethylcyclopropanecarboxylic acid and cyano(3-phenoxyphenyl)methanol.?? ??
Colorless solid. Insoluble in water. Used as a wide spectrum insecticide.??? ?? ??
Insoluble in water.?? ???
Cyhalothrin is a trifluoromethyl pyrethrine derivative.?? ?? ??
Cyhalothrin is similar in structure to cypermethrin but with one of the chlorine atoms replaced by a trifluoromethyl group. This substitution appears to result in greater lipophilicity. Cyhalothrin is used in animal health and the more active isomer mixture, lambda-cyhalothrin, has the main crop use. Only a limited amount of information has been published in the scientific literature. What is available indicates that the metabolism and environmental fate of the cyhalothrins are very similar to those of cypermethrin. Both compounds have been the subject of UK Pesticide Safety Directorate evaluations (referred to as PSD in parentheses below).????? ?? ?? ? ???
???
?? ??
????? ?? ??
???( 150)?? ??
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