Divinylbenzenes

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Divinylbenzenes
Surname o -divinylbenzene m -divinylbenzene p -divinylbenzene
other names 1,2-divinylbenzene,
1,2-diethenylbenzene
1,3-divinylbenzene,
1,3-diethenylbenzene
1,4-divinylbenzene,
1,4-diethenylbenzene
Structural formula Structure of 1,2-divinylbenzene Structure of 1,3-divinylbenzene Structure of 1,4-divinylbenzene
CAS number 91-14-5 108-57-6 105-06-6
1321-74-0 (mixture of isomers)
PubChem 66666 7941 66041
Molecular formula C 10 H 10
Molar mass 130.19 g mol −1
Physical state liquid firmly
Brief description water-clear, irritating to the mucous membranes,
easily polymerizable, flammable liquid
combustible solid
Melting point −67 ° C −67 ° C 31 ° C
boiling point 200 ° C 200 ° C 95–96 ° C (24 hPa )
solubility - 52 mg / l (25 ° C) practically insoluble in water
GHS
labeling
07 - Warning 09 - Dangerous for the environment
Caution
no classification available
07 - Warning 09 - Dangerous for the environment
Caution
H and P phrases 315-319-335-411 see above 315-319-335-411
no EUH phrases see above no EUH phrases
273-302 + 352-304 + 340
305 + 351 + 338
see above 273-302 + 352-304 + 340
305 + 351 + 338

The divinylbenzenes are aromatic hydrocarbons having the general formula C 10 H 10 . They consist of a benzene ring with two vinyl groups  (–CH = CH 2 ) as substituents . Their different arrangement ( ortho , meta or para ) result in three constitutional isomers . Technical divinylbenzene is a mixture of the ortho , meta and para isomers (1,2-, 1,3- and 1,4-divinylbenzene).

properties

o - and m -Divinylbenzene are water-clear, mucous membrane-irritating, easily polymerizable, flammable liquids. The p -divinylbenzene, which has the highest symmetry, has the highest melting point and is a solid. They are insoluble in water.

use

Divinylbenzenes are mainly used as crosslinkers in the production of styrene copolymers , which results in reduced solubility in most organic solvents , improved heat resistance, higher hardness and strength without affecting the appearance or optical and electrical properties. By far the largest amount is consumed in the production of copolymers with styrene derivatives for use as ion exchange material . As a rule, technical mixtures are polymerized with a proportion of 55% or 80%.

Individual evidence

  1. Entry for CAS no. 1321-74-0 in the GESTIS substance database of the IFA , accessed on March 13, 2017(JavaScript required) .
  2. a b c d Entry on 1,2-divinylbenzene in the GESTIS substance database of the IFA , accessed on March 13, 2017(JavaScript required) .
  3. a b c Entry on 1,3-divinylbenzene in the GESTIS substance database of the IFA , accessed on March 13, 2017(JavaScript required) .
  4. a b c d Entry on 1,4-divinylbenzene in the GESTIS substance database of the IFA , accessed on March 13, 2017(JavaScript required) .