Sesamex

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Structural formula
Structure of sesoxane
Structural formula without stereochemistry
General
Surname Sesamex
other names
  • ( RS ) -5- [1- [2- (2-ethoxyethoxy) ethoxy] ethoxy] -1,3-benzodioxole
  • ( RS ) -5- (3,6,9-trioxa-2-undecyloxy) benzo [ d ] -1,3-dioxolane
  • (±) -5- [1- [2- (2-ethoxyethoxy) ethoxy] ethoxy] -1,3-benzodioxole
  • (±) -5- (3,6,9-Trioxa-2-undecyloxy) benzo [ d ] -1,3-dioxolane
  • 5- [1- [2- (2-ethoxyethoxy) ethoxy] ethoxy] -1,3-benzodioxole
  • 5- (3,6,9-trioxa-2-undecyloxy) benzo [ d ] -1,3-dioxolane
  • Sesoxane
  • SES
Molecular formula C 15 H 22 O 6
Brief description

straw yellow liquid

External identifiers / databases
CAS number 51-14-9
ECHA InfoCard 100.149.223
PubChem 5796
Wikidata Q2800151
properties
Molar mass 298.33 g mol −1
Physical state

liquid

solubility

very sparingly soluble in water: 0.155 g l −1 (20 ° C)

safety instructions
GHS hazard labeling from  Regulation (EC) No. 1272/2008 (CLP) , expanded if necessary
07 - Warning

Caution

H and P phrases H: 302
P: ?
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Sesamex ( Sesoxan ) acts as a synergist and strengthens the insecticidal effect of other insecticides such as pyrethrins , pyrethroids or carbamates . Taken by itself, it has no effect on insects. It was developed in 1950 by Morten Beroza from the Agricultural Research Service based on sesamol .

Admission

Sesamex is not approved as a crop protection agent in the European Union or Switzerland .

Individual evidence

  1. ↑ NP Cheremisinoff, JA King: Toxic Properties of Pesticides . Marcel Dekker Inc, 1994 ( limited preview in Google Book Search).
  2. ↑ Entry on Sesamex in the Pesticide Properties DataBase (PPDB) of the University of Hertfordshire , accessed on May 6, 2014.
  3. ↑ Entry on 5- (3,6,9-Trioxa-2-undecyloxy) benzo (d) -1,3-dioxolane in the GESTIS substance database of the IFA , accessed on July 10, 2016(JavaScript required) .
  4. ↑ Entry on 5- (3,6,9-trioxa-2-undecyloxy) benzo (d) -1,3-dioxolane in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Distributors can expand the harmonized classification and labeling .
  5. ↑ Patent US2832792 : 3,4-methylenedioxyphenyl acetals as synergists for pyrethrins. Registered on June 15, 1955 , published April 29, 1958 , inventor: Morten Beroza. ‌
  6. ^ Directorate-General for Health and Food Safety of the European Commission: EU pesticide database ; Entry in the national directory of plant protection products in Switzerland ; Retrieved June 25, 2016.