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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Skin sensitisation

Currently viewing:

Administrative data

Endpoint:
skin sensitisation: in vivo (LLNA)
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2010
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2010
Report date:
2010

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
GLP compliance:
yes
Type of study:
mouse local lymph node assay (LLNA)

Test material

Constituent 1
Chemical structure
Reference substance name:
Triisotridecyl phosphite
EC Number:
278-758-9
EC Name:
Triisotridecyl phosphite
Cas Number:
77745-66-5
Molecular formula:
C39H81O3P
IUPAC Name:
tris(2-methylnonacosyl) phosphite

In vivo test system

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified

Study design: in vivo (LLNA)

Vehicle:
acetone/olive oil (4:1 v/v)
Concentration:
25%, 50%, 100%
No. of animals per dose:
3
Statistics:
EC3= 92.1%

Results and discussion

In vivo (LLNA)

Resultsopen allclose all
Parameter:
SI
Value:
1.25
Test group / Remarks:
25% concentration
Parameter:
SI
Value:
2.31
Test group / Remarks:
50% concentration
Parameter:
SI
Value:
3.13
Test group / Remarks:
100% concentration

Any other information on results incl. tables

Concentration

dpm/node

Test / Control Ratio

Vehicle (acetone/olive oil 4:1)

756.88

N/A

25%

942.43

1.25

50%

1746.07

2.31

100%

2367.08

3.13

EC3= 92.1%

Applicant's summary and conclusion

Interpretation of results:
sensitising
Remarks:
Migrated informationweak
Conclusions:
Test substance was only postive (ratio >3) at a concentration of 100%, with an EC3 of 92.1%. While this substance is classifiable as a skin sensitiser based on these results, it would only be a weak sensitiser.
Executive summary:

TiTDP was test using the LLNA assay at concentrations of 25%, 50%, and 100%. It was only just barely positive at the 100% concentration. The calculated EC3 value is 92.1%. The results suggest that while TiTDP will be classified as a skin sensitiser (since there is only one category for skin sensitisers) it is expected to be only a weak skin sensitiser.