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Home > Encyclopedia > Propetamphos

Propetamphos

Propetamphos structure

Propetamphos 

structure
  • CAS No:

    31218-83-4

  • Formula:

    C10H20NO4PS

  • Chemical Name:

    Propetamphos

  • Synonyms:

    2-Butenoic acid,3-[[(ethylamino)methoxyphosphinothioyl]oxy]-,1-methylethyl ester,(2E)-;Crotonic acid,3-hydroxy-,isopropyl ester,O-ester with O-methyl ethylphosphoramidothioate,(E)-;2-Butenoic acid,3-[[(ethylamino)methoxyphosphinothioyl]oxy]-,1-methylethyl ester,(E)-;Blotic;SAN 322I;Propetamphos;VEL 4283;SAN 322;Safrotin S 200;Ectomort Jetting Fluid and Sheep Dip;Deadmag;Ectomort Jetting Fluid;Magget;Mules-n-Mark II;E-Propetamphos;Ectomort Centenary;Young's Summer Dip;Safrotin MC;Safrotin;Safrotin Brush-on Bait

  • Categories:

    Agrochemicals  >  Insecticides

Description

Propetamphos technical is a yellowish, oily liquid at room temperature and a moderately toxic acaricide and insecticide. It is sparingly soluble in water, but very soluble in acetone, chloroform, ethanol, and hexane. The US EPA has classifi ed propetamphos as a GUP and RUP, indicating that its handling should be done by certifi ed, qualifi ed applicators. Propetamphos is used for the control of cockroaches, fl ies, ants, ticks, moths, fl eas, and mosquitoes in households and where vector eradic

Propetamphos Basic Attributes

281.31

281.31

250-517-2

2931900090

Characteristics

88.9

3.82

1.1294 g/cm3 @ Temp: 20 °C

<25 °C

87-89 °C @ Press: 5 x 10-3 Torr

148.0±28.4 °C

1.495

In water, 1.10X10+2 mg/l @ 24 deg C

APPROX 4°C

1.9×10 -3 Pa (20°C)

LD50 orally in male rats: 82 mg/kg (Berg, Gothe)

Safety Information

II

6.1(b)

3018

3

25-50/53

37-45-60-61

GQ4750000

T,N

Stable during storage (shelf life > or = 2 yr at 20 deg C) & to light. Stable in aqueous soln (5 ppm level) in sunlight; no degradation during 70 hr.

P260-P273-P280-P284-P301 + P310 + P330-P304 + P340 + P310

H301 + H311-H330-H410

Propetamphos Use and Manufacturing

Methods of Manufacturing

In the presence of a catalyst and an acid-binding agent, the intermediate obtained from the reaction of isopropyl 3-hydroxybutenoate with thiophosphoryl chloride is then condensed with methanol and ethylamine to produce dimethoate. In industrial production, add tributylamine to the mixture of isopropyl acetoacetate and thiophosphoryl chloride. Stir and cool at -3°C when feeding, continue to stir at 0-3°C for 4.5h, separate the viscous oily liquid, add toluene, Petroleum ether, filtered off tributylammonium chloride, the filtrate was concentrated in vacuo at a bath temperature of 30 ℃, methanol was added to the residue, as quickly as possible to 0 ℃, stirred for 4h, then add 70% ethylamine in water, feed Temperature -5℃, mix at 0℃ and stir for 4.5h. The reaction mixture was extracted twice with about 10% hydrochloric acid solution. Petroleum ether was added during the second extraction to facilitate extraction. The petroleum ether was washed with water and alkali, dried over anhydrous sodium sulfate, and the solvent was removed to obtain methoprene. Raw material consumption quota: 670kg/t of tributylamine, 520kg/t of isopropyl acetoacetate, 650kg/t of thiophosphoryl chloride, 470kg/t of methanol, and 820kg/t of ethylamine (70%).

Uses

Insecticide.

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