Ipsdienol

from Wikipedia, the free encyclopedia
Structural formula
Ipsdienol
Ipsdienol without specifying the stereochemistry
General
Surname Ipsdienol
other names

2-methyl-6-methylene-2,7-octadien-4-ol

Molecular formula C 10 H 16 O
Brief description

oil

External identifiers / databases
CAS number
  • 14434-41-4 (unspec.)
  • 60894-97-5 [( R ) -Ipsdienol]
  • 35628-00-3 [( S ) -Ipsdienol]
EC number 238-408-8
ECHA InfoCard 100.034.901
PubChem 85734
Wikidata Q55756695
properties
Molar mass 152.23 g mol −1
Physical state

liquid

safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Ipsdienol is a chemical compound from the group of terpene alcohols and a pheromone of various bark beetle species of the genus Ips .

Isomers

Ipsdienol has a stereogenic center on the carbon atom in position 4 and thus occurs in the form of two enantiomers : ( R ) - (-) - Ipsdienol and ( S ) - (+) - Ipsdienol.

Isomers of Ipsdienol
Surname ( S ) -Ipsdienol ( R ) -Ipsdienol
other names (+) - Ipsdienol (-) - Ipsdienol
Structural formula (S) -Ipsdienol Structural Formula.svg (R) -Ipsdienol Structural Formula.svg
CAS number 35628-00-3 60894-97-5
14434-41-4 (unspec.)
EC number 609-154-9 -
238-408-8 (unspec.)
ECHA info card 100.128.974 -
100.034.901 (unspec.)
PubChem 92301 181296
85734 (unspec.)
Wikidata Q13422964 Q27158231
Q55756695 (unspec.)

Occurrence

The ( R ) - enantiomer is from Ips confusus used, a pest of ponderosa pine , while the ( S ) -enantiomer of a pheromone Ips paraconfusus is.

Individual evidence

  1. a b Entry on Ipsdienol. In: Römpp Online . Georg Thieme Verlag, accessed on February 11, 2015.
  2. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  3. Jean Pierre Vité , Wittko Francke : Forest protection against bark beetles: From the catch tree to the trap . In: Chemistry in Our Time . tape  19 , no. 1 , February 1985, p. 11–21 , doi : 10.1002 / ciuz.19850190103 ( PDF ).