ETHIOFENCARB Chemical Properties

Melting point:

43-45℃

Boiling point:

327.3±34.0 °C(Predicted)

Density 

1.231 g/cm³ (20 ºC)

vapor pressure 

4.5 x 10^-4 Pa (20 °C)

refractive index 

1.4790 (estimate)

storage temp. 

APPROX 4°C

Water Solubility 

1800 mg l^-1 (20 °C)

pka

12.09±0.46(Predicted)

BRN 

2973224

CAS DataBase Reference

29973-13-5(CAS DataBase Reference)

EPA Substance Registry System

Ethiofencarb (29973-13-5)

Safety Information

Hazard Codes 

Xn,N

Risk Statements 

22-50/53

Safety Statements 

60-61

RIDADR 

2992

WGK Germany 

3

RTECS 

FC2628000

HazardClass 

6.1(b)

PackingGroup 

III

HS Code 

29309090

Hazardous Substances Data

29973-13-5(Hazardous Substances Data)

Toxicity

LC50 (96-hour) for carp 10–20 mg/L, golden orfe 8–10 mg/L, goldfish 20–40 mg/L and rudd 10–20 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats 411–499 mg/kg (Hartley and Kidd, 1987), 200 mg/kg (RTECS, 1985).

ETHIOFENCARB Usage And Synthesis

Description

Ethiofencarb, α-ethylthio o-tolyl methylcarbamate (IUPAC), C11H25N02S, MW 225.3, mp 33.4 ?C, forms colorless crystals that are moderately soluble in water, are fairly soluble in hexane, and are readily soluble in dichloromethane, isopropanol, and toluene.

Uses

Ethiofencarb is a systemic insecticide with contact and stomach action. It is used to control aphids on fruit, vegetables, ornamentals and sugar beet.

Uses

Ethiofencarb is a kind of Systemic insecticide ,used to control aphids on fruit crops.

Preparation

Ethiofencarb is produced by reaction of 2-chloromethyl phenol with sodium ethylmercaptide to form 2-ethylthio methylphenol, which in turn is reacted with methylisocyanate.

Definition

ChEBI: Ethiofencarb is a carbamate ester. It has a role as a carbamate insecticide, an EC 3.1.1.7 (acetylcholinesterase) inhibitor and an agrochemical. It is functionally related to a methylcarbamic acid and a 2-[(ethylsulfanyl)methyl]phenol.

Environmental Fate

Plant. Degrades in plants to the sulfone and sulfoxide (Hartley and Kidd, 1987).

Metabolic pathway

Ethiofencarb is metabolised by rapid oxidation at sulfur, hydrolysis of the carbamate group to give phenols, hydroxylation of the N-methyl moiety and conjugation.

Degradation

Ethiofencarb is stable in neutral and acidic but is hydrolysed under basic conditions. DT₅₀ values at pH 7 and 11.4 (37 °C) were 450 hours and 5 minutes, respectively. The kinetics of hydrolysis of ethiofencarb in pure water and in aqueous solutions at pH 2,6,9,12 and at temperatures in the range 4-50°C were studied. No acid hydrolysis was observed. Ethiofencarb was rapidly hydrolysed at pH 9 and 12. Ethiofencarb in pure water at room temperature reached an equilibrium with 80% remaining undegraded (Sanz-Asensio et al., 1997).
Photodegradation of aqueous solutions in sunlight is rapid (PM). The oxidative photodegradation of ethofencarb was studied in aqueous acetonitrile using anthraquinone to mimic natural photosensitisers. Solutions were irradiated with a Hg lamp (400 W) for 48 minutes. The emission spectrum of the lamp was not described. Reaction products were identified by GC-MS methods. The main products were 2- hydroxybenzaldehyde (2) and 3-methylbenzo[e-1,3]oxazine-2,4-dione(3) (see Scheme 1). Products resulted from photocleavage of the CH,-S bond and/or the C-O bond followed by hydrogen atom abstraction and photo-oxidation. An electron-acceptor photosensitiser may increase rates of photodegradation (Galadi and Julliard, 1996). Solutions of ethiofencarb in cyclohexane, cyclohexene or isopropanol were irradiated with a high pressure Hg lamp (cut-off filter <280 nm) or natural sunlight (Germany, May-July). Analysis was by HPLC with diode-array detection, NMR, IR and MS. Half-lives of photodegradation were in the range 20 minutes to more than 20 hours. The predominant reaction (Scheme 1) was photo-oxidation of ethiofencarb to its sulfoxide (4). The cyclic dione (3) was a product of oxidation at the benzylic position. Ethiofencarb was photo-oxidised in cyclohexane to the sulfoxide (4) and the sulfone (5) and their corresponding phenols (8 and 9), the latter being a minor product. Subsequently the cyclised dione (3) was formed. In isopropanol, reaction with solvent gave addition products (6 and 7) and an unusual bis-diethylthio compound (10) (Kopf and Schwack, 1995).

ETHIOFENCARB(29973-13-5)Related Product Information

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• BENDIOCARB
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• (-)-MENTHYL CHLOROFORMATE
• ETHIOFENCARB-SULFONE
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