MEVINPHOS

MEVINPHOS Struktur
26718-65-0
CAS-Nr.
26718-65-0
Englisch Name:
MEVINPHOS
Synonyma:
DURAPHOS;PHOSDRIN;MEVINPHOS;MEVINDRIN;OS-2046(R);E-MEVINPHOS;PHOSDRIN (TM);TRANS-MEVINPHOS;cis-Duraphos(TM);formerly 298-01-1
CBNumber:
CB9177587
Summenformel:
C7H13O6P
Molgewicht:
224.15
MOL-Datei:
26718-65-0.mol

MEVINPHOS Eigenschaften

Dampfdruck
1.7×10-2 Pa (20 °C)
storage temp. 
0-6°C
Wasserlöslichkeit
Totally miscible

Sicherheit

MEVINPHOS Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Mevinphos is used to control chewing and sucking insects in a wide range of crops.

Stoffwechselwegen

Technical mevinphos consists of two stereochemical isomers in the E:Z ratio of about 7:3. Mevinphos is characterised by a high rate of metabolic breakdown, such that crops can be harvested within a few hours of its application. The compound is also rapidly translocated within plants. There are considerable differences in the metabolism of the two isomers. In general, the E-isomer (the more toxic, more active acetylcholinesterase inhibitor and more effective insecticide) is detoxified more quickly in plants but more slowly in animals. The major route of detoxification in plants is through hydrolysis to give dimethyl phosphate and methyl acetoacetate with hydrolysis of the carboxylic ester function being of lesser importance. Demethylation of the more toxic Eisomer via a glutathione-based transalkylation reaction is an important route in mammals, whereas the 2-isomer is hydrolysed to dimethyl phosphate .

Degradation

Mevinphos is hydrolysed in alkaline solutions (PM). The DT50s for the technical material at pH 6, 7 and 10 were 94 days, 30 days and 8 hours respectively (Porter et al., 1964). The E-isomer (1) is hydrolysed more quickly than the Z-isomer (2). Under alkaline conditions, the products of hydrolysis of the E-isomer were shown to be dimethyl phosphate (3), monomethyl phosphate (4), acetone (S), the E-mevinphos carboxylic acid (6) and the desmethyl E-mevinphos carboxylic acid (7). A small amount of desmethyl E-mevinphos (8) was also detected. The Z-isomer gave very little of the desmethyl Z-mevinphos carboxylic acid (10) indicating that the attack of hydroxyl ion on the 2-isomer was almost entirely on phosphorus, whereas there was additional nucleophilic attack on the carboxylic ester function in the case of the E-isomer which was shown to gwe dimethyl phosphate (3) and acetone (5). Acid hydrolysis resulted in demethylation of both isomers with the desmethyl E-mevinphos (8) and desmethyl Z-mevinphos (9) being detected in addition to dimethyl phosphate (3) and monomethyl phosphate (4) (Spencer et al., 1958) (see Scheme 1).

MEVINPHOS Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


MEVINPHOS Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 21)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873
sales@chemdad.com China 39916 58
Spectrum Chemical Manufacturing Corp. 021-021-021-67601398-809-809-809 15221380277
marketing_china@spectrumchemical.com China 9664 60
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-0755-85201366 18938635012
sales@regentsciences.com China 9293 58

26718-65-0()Verwandte Suche:


  • Dimethyl methoxycarbonyl propenyl phosphate
  • E-MEVINPHOS
  • E-MEVINPHOS (TRANS)
  • DURAPHOS
  • MEVINDRIN
  • MEVINPHOS
  • 3-HYDROXY-CROTONIC ACID METHYL ESTER DIMETHYL PHOSPHATE
  • 2-METHOXYCARBONYL-1-METHYLVINYL DIMETHYL PHOSPHATE
  • 2-CARBOMETHOXY-1-METHYLVINYLDIMETHYL PHOSPHATE
  • e-mevinphos (cis-butenoic acid)
  • formerly 298-01-1
  • TRANS-MEVINPHOS
  • mevinphos(stereochemistryunspecified)
  • OS-2046(R)
  • PHOSDRIN
  • PHOSDRIN (TM)
  • cis-Duraphos(TM)
  • E-Mevinphos Solution
  • Vinblastine Impurity 10
  • 26718-65-0
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