Simazine

Last updated
Simazine
Simazine.svg
Simazine-3D-spacefill.png
Names
Preferred IUPAC name
6-Chloro-N2,N4-diethyl-1,3,5-triazine-2,4-diamine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.004.124 OOjs UI icon edit-ltr-progressive.svg
KEGG
PubChem CID
UNII
  • InChI=1S/C7H12ClN5/c1-3-9-6-11-5(8)12-7(13-6)10-4-2/h3-4H2,1-2H3,(H2,9,10,11,12,13) Yes check.svgY
    Key: ODCWYMIRDDJXKW-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C7H12ClN5/c1-3-9-6-11-5(8)12-7(13-6)10-4-2/h3-4H2,1-2H3,(H2,9,10,11,12,13)
    Key: ODCWYMIRDDJXKW-UHFFFAOYAN
  • Clc1nc(nc(n1)NCC)NCC
Properties
C7H12ClN5
Molar mass 201.66 g·mol−1
AppearanceWhite crystalline powder
Density 1.3 g/cm3
Melting point 225–227 °C (437–441 °F; 498–500 K)
5 mg/L
Solubility in other solventsSoluble in methanol, chloroform, and diethyl ether; slightly soluble in pentane
log P 1.9600
Vapor pressure 0.000810 mPa at 20 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Simazine is an herbicide of the triazine class. The compound is used to control broad-leaved weeds and annual grasses.

Contents

Preparation

Simazine may be prepared from cyanuric chloride and a concentrated solution of ethyl amine (at least 50 percent by number) in water. [1] The reaction is highly exothermic and is therefore best carried out in an ice bath below 10 °C. It is also essential to carry out the synthesis in a fume hood since cyanuric chloride decomposes at high temperatures into hydrogen chloride and hydrogen cyanide, both of which are highly toxic by inhalation.

Properties and uses

Simazine is an off-white crystalline compound which is sparingly soluble in water. It is a member of the triazine-derivative herbicides, and was widely used as a residual non-selective herbicide, but is now banned in European Union states. [2] Like atrazine, a related triazine herbicide, it acts by inhibiting photosynthesis. It remains active in the soil for two to seven months or longer after application.

See also

Related Research Articles

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References

  1. "Simazine: Methods of Manufacturing". PubChem.
  2. "EU directive 91/414/EEC".