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The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Ecotoxicological information

Biological effects monitoring

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Administrative data

Endpoint:
biological effects monitoring
Type of information:
other: synthesis of data
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: No experimental results but is a good synthesis on the natural occurrence and effects of salicylic acid and derivatives.

Data source

Reference
Reference Type:
review article or handbook
Title:
The natural history of salicylic acid, plant product and animal medicine.
Author:
Pierpoint W.S.
Year:
1997
Bibliographic source:
Interdisciplinary Science Rev. 22 :45-52

Materials and methods

Test material

Constituent 1
Chemical structure
Reference substance name:
Salicylic acid
EC Number:
200-712-3
EC Name:
Salicylic acid
Cas Number:
69-72-7
Molecular formula:
C7H6O3
IUPAC Name:
2-hydroxybenzoic acid

Results and discussion

Any other information on results incl. tables

Memo: influence of salicin in leaves on potential predators on these leaves.

The presence of salicin in willow leaves along with more complex  compounds that can be hydrolysed to it would be expected to influence  potential 

predators on these leaves. 

A number of studies have emphasised  the ecological effects of these compounds and have suggested that they do help determine the feeding 

preferences of such herbivores as the New  Zealand opossum, Arctic snowshoe hares, and a range of insects including  moths, butterflies, 

weevils, and sawflies. Most usually they act as  feeding deterrents although somme studies suggest more complex effects on  host-herbivore interactions. 

Thus salicin and populin appear to stimulate  the feeding of 2 beetles, Chrysomela vigintipunctata costella and  Plagiodera versicolora distincta. 

Chrysomelid beetles are believed to  hydrolyse salicin derivatives, oxidise the salicyl alcohol, 

and store or  secrete this as a deterrent aldehyde against ants and other arthropod  predators.

Applicant's summary and conclusion