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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

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

Administrative data

Endpoint:
basic toxicokinetics
Type of information:
other: Expert review
Adequacy of study:
key study
Study period:
April 2014
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Referenceopen allclose all

Reference Type:
other:
Title:
Unnamed
Year:
2014
Report date:
2014
Reference Type:
publication
Title:
A toxicological and dermatologic assessment of salicylates when used as fragrance ingredients
Author:
Belsito, D., Bickers, D., Bruze, M., Calow, P., Greim, H., Hanifin, J.M., Rogers, A.E., Saurat, J.H., Sipes, I.G., and Tagami, H.
Year:
2007
Bibliographic source:
Food and Chemical Toxicology 45:S318-S361
Reference Type:
publication
Title:
SIDS Initial Assessment Profile: Long Chain Alcohols (C6-C22 primary aliphatic alcohols)
Author:
OECD
Year:
2006
Bibliographic source:
SIAM 22, April 18-21

Materials and methods

Objective of study:
other: Expert review and summary of available information
Principles of method if other than guideline:
Expert review of the toxicokinetic properties of the subject material based on physical-chemical parameters and available published information.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
431-090-3
EC Name:
-
Cas Number:
190085-41-7
Molecular formula:
C19 H30 O3
IUPAC Name:
2-butyloctyl 2-hydroxybenzoate
Radiolabelling:
no

Test animals

Species:
other: not applicable

Administration / exposure

Route of administration:
other: oral, dermal and inhalation
Details on exposure:
See information in this endpoint summary

Results and discussion

Applicant's summary and conclusion

Conclusions:
Once absorbed from the GI tract, lungs or skin, the subject material is expected to be rapidly metabolized and eliminated predominantly through the urine. As conservative estimates, oral and inhalation bioavailability are presumed to be 100%. Based on the physical-chemical properties of the subject material as well as on data for similar salicylate esters, dermal absorption through human skin should be minimal. A conservative estimate of 10% dermal absorption is assigned.