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m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat

D-Phenothrin Struktur
26046-85-5
CAS-Nr.
26046-85-5
Bezeichnung:
m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat
Englisch Name:
D-Phenothrin
Synonyma:
D-PHENOTHRIN;D-permethrin;D-trans-Phenot;D-TRANS-PHENOTHRIN;rich-d-t-Phenothrin;(-)-trans-Phenothrin;(1r)-trans-phenothrin;Pesticide D-Phenothrin;(1r-trans)-henyl)methyleste;D-Phenothrin, 10 mM in DMSO
CBNumber:
CB9699395
Summenformel:
C23H26O3
Molgewicht:
350.45
MOL-Datei:
26046-85-5.mol

m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat Eigenschaften

Siedepunkt:
437.0±45.0 °C(Predicted)
Dichte
1.120±0.06 g/cm3(Predicted)
Dampfdruck
1.9×10-5Pa (21.4 °C)
storage temp. 
Sealed in dry,2-8°C
L?slichkeit
Chloroform (Slightly), Methanol (Slightly)
Aggregatzustand
Oil
Wasserl?slichkeit
<0.01 mg l-1 (25 °C)
Farbe
Colourless to Dark Yellow
CAS Datenbank
26046-85-5(CAS DataBase Reference)
EPA chemische Informationen
d-Phenothrin (26046-85-5)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Toxizit?t LD50 oral in mouse: > 10gm/kg
Bildanzeige (GHS) Environment (GHS09)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gew?ssergef?hrdend Kategorie 1 Warnung P273, P391, P501
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P391 Verschüttete Mengen aufnehmen.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Phenothrin is used for the control of insects for public health. It is also used to protect stored grain.

Stoffwechselwegen

Phenothrin is the name given to the 1RS-cis-trans isomer mixture (racemic). The product now used is d-phenothrin which is 95% 1R and 75% trans. It has no field use because the chrysanthemate moiety is very sensitive to photodegradation. Nevertheless, information on its photochemistry and its fate in soils and plants has been published. Several studies in rodents have been reported; this is a reflection of its use in public health. Phenothrin is degraded mainly by photo-oxidation and by hydrolysis and oxidation in plants and animals.

Degradation

Phenothrin is stable under normal storage conditions but it is labile to base, being hydrolysed to trans-2,2-dimethyl-3-(2-methylprop-1-enyl)- cyclopropanecarboxylic acid (11, trans-chrysanthemic acid) and 3-phenoxybenzyl alcohol (13,3PBAlc) (Scheme 2). It is sensitive to light and, for example, as a thin film at midday in the summer at 55 ° N, it was degraded with a DT50 of 2.5-3.0 hours (Samsonov and Makarov, 1996).
When (lR)-trans-[14C-carboxyl]phenotwhraisn irradiated in degassed benzene solution, the only product was the cis-isomer. However, in oxygenated benzene solution, degradation was about 10-fold faster and many products were detected (Ruzo et al., 1982). A similar array of products was seen on exposure of thin films to sunlight. Major products (Scheme 1) were formed by oxidation at the isobutylene substituent giving the epoxide (2), the alcohol (3), the aldehyde (4) and the carboxylic acid (5). Caronaldehyde (6) and the caronic acid derivative (7) were formed by cleavage of ozonolysis products and the hydroperoxide (8) was formed by ene reactions at the 1’-position. Ester cleavage to 3PBAlc, 3PBAl and 3PBA (not shown in Scheme 1) was relatively minor.

m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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26046-85-5(m-Phenoxybenzyl-(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropancarboxylat)Verwandte Suche:


  • (1R)-2β-(2-Methyl-1-propenyl)-3,3-dimethylcyclopropane-1α-carboxylic acid m-phenoxybenzyl ester
  • (1R)-3,3-Dimethyl-2β-(2-methyl-1-propenyl)cyclopropane-1α-carboxylic acid 3-phenoxybenzyl ester
  • (1R,3R)-2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid 3-phenoxybenzyl ester
  • (1R,3R)-2,2-Dimethyl-3α-(2-methyl-1-propenyl)cyclopropanecarboxylic acid (3-phenoxyphenyl)methyl ester
  • (1R-trans)-2,2-Dimethyl-3-(2-methyl-1-propenyl)-cyclopropanecarboxylic acid
  • D-trans-Phenot
  • (1r)-trans-phenothrin
  • (1r-trans)-henyl)methyleste
  • 2,2-dimethyl-3-(2-methyl-1-propenyl)-,(3-phenoxyphenyl)methylester,(1r-trans)-cyclopropanecarboxylicaci
  • D-TRANS-PHENOTHRIN
  • D-PHENOTHRIN
  • (1R-trans)-2,2-Dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid-(3-phenoxyphenyl)methyl ester-
  • d-trans-phenothrin (bsi,ido,ban)
  • (1R-trans)-2,2-Dimethyl-3-(2-methyl-1-propenyl)-cyclopropanecarboxylic acid, (3-phenoxyphenyl)methyl ester
  • 3-Phenoxybenzyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
  • 3-PHENOXYBENZYL(+)-TRANS-CHRYSANTHEMATE
  • rich-d-t-Phenothrin
  • (1R)-2,2-Dimethyl-3α-(2-methyl-1-propenyl)cyclopropane-1β-carboxylic acid 3-phenoxybenzyl ester
  • m-phenoxybenzyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
  • Pesticide D-Phenothrin
  • (3-phenoxyphenyl)methyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
  • (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)-1-cyclopropanecarboxylic acid (3-phenoxyphenyl)methyl ester
  • Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-, (3-phenoxyphenyl)methyl ester, (1R,3R)-
  • (-)-trans-Phenothrin
  • (1R,3R)-3-Phenoxybenzyl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
  • D-permethrin
  • D-trans-Phenothrin in Acetonitrile
  • 3-phenoxybenzyl(1R,3R)-2,2-dimethyl- 3-(2-methylprop-1- enyl)cyclopropanecarboxylate (1R-trans-Phenothrin)
  • D-Phenothrin, 10 mM in DMSO
  • 26046-85-5
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