Propetamphos

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Structural formula
Structural formula of Propetamphos
General
Surname Propetamphos
other names
  • O - (2- (Isopropoxycarbonyl) -1-methyl) vinyl- O -methyl- (ethylamido) thiophosphate
  • Safrotine
  • Seraphos (?)
Molecular formula C 10 H 20 NO 4 PS
Brief description

yellowish, oily liquid

External identifiers / databases
CAS number 31218-83-4
EC number 250-517-2
ECHA InfoCard 100.045.910
PubChem 5372405
Wikidata Q18629963
properties
Molar mass 281.31 g mol −1
Physical state

liquid

density

1.1294 g cm −3

boiling point

87-89 ° C (0.007 hPa )

solubility

very heavy in water (0.11 g l −1 at 24 ° C)

Refractive index

1.495

safety instructions
GHS hazard labeling from  Regulation (EC) No. 1272/2008 (CLP) , expanded if necessary
06 - Toxic or very toxic 09 - Dangerous for the environment

danger

H and P phrases H: 301-410
P: 273-301 + 310-501
Toxicological data
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Propetamphos is a chemical compound from the group of thiophosphoric acid esters . The compound has been used as an insecticide against hygiene pests.

Extraction and presentation

Propetamphos can be prepared from isopropyl acetoacetate and thiophosphoryl trichloride . Their product reacts with methanol and ethylamine to form the end product.

Individual evidence

  1. a b Crop Protection Handbook 2014 . 100th edition. MeisterPro, Willoughby, Ohio 2014, pp. 491 .
  2. a b c d e f Entry on Propetamphos in the GESTIS substance database of the IFA , accessed on February 1, 2016(JavaScript required) .
  3. Metabolic Pathways of Agrochemicals, p. 462.
  4. Entry on trans-isopropyl-3 - [[(ethylamino) methoxyfosfinothioyl] oxy] crotonate Template: Linktext-Check / Escaped in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
  5. Thomas A. Unger: Pesticide Synthesis Handbook . William Andrew, 1996, ISBN 0-8155-1853-6 , pp. 381 ( limited preview in Google Book Search).