Prometon

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Structural formula
Prometon structural formula
General
Surname Prometon
other names

2,4-bis (isopropylamino) -6-methoxy-1,3,5-triazine

Molecular formula C 10 H 19 N 5 O
Brief description

white solid

External identifiers / databases
CAS number 1610-18-0
EC number 216-548-0
ECHA InfoCard 100.015.044
PubChem 4928
Wikidata Q7249739
properties
Molar mass 225.29 g mol −1
Physical state

firmly

density

1.088 g cm −3

Melting point

91-92 ° C

solubility

very sparingly soluble in water (750 mg l −1 at 20 ° C)

safety instructions
GHS labeling of hazardous substances
07 - Warning

Caution

H and P phrases H: 302-315-319-335
P: 261-305 + 351 + 338
Toxicological data
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Prometon is a chemical compound belonging to the methoxy triazine group .

Extraction and presentation

Prometon can be obtained by reacting propazine with methanol in the presence of sodium hydroxide or by reacting propazine with sodium methoxide .

Prometon synthesis.svg

properties

Prometon is a white, flammable solid that is very sparingly soluble in water.

use

Prometon is used as a herbicide against perennial grasses and leaf weeds. It works by inhibiting photosynthesis and influences photosystem II by competing with plastoquinone and thus disrupting electron transport processes. It was first approved in the United States in May 1959.

Admission

Prometon is not included in the list of active ingredients of plant protection products permitted in the European Union. In Germany, Austria and Switzerland, no pesticides with this active ingredient are permitted.

Individual evidence

  1. a b c d e f g h i j Entry for CAS no. 1610-18-0 in the GESTIS substance database of the IFA , accessed on July 12, 2013(JavaScript required) .
  2. a b c EPA: Reregistration Eligibility Decision for Prometon (PDF; 616 kB), March 25, 2008.
  3. ^ Entry on Prometon in the Hazardous Substances Data Bank , accessed July 12, 2013.
  4. Thomas A. Unger: Pesticide synthesis handbook . 1996, ISBN 978-0-8155-1401-5 ( limited preview in Google Book Search).
  5. ^ Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national registers of plant protection products in Switzerland , Austria and Germany ; Retrieved February 19, 2016.