Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: EC Method B.6. (Guinea Pig Maximisation Test) OECD Guideline No. 406
GLP compliance:
yes

In vivo test system

Test animals

Species:
other: Guinea pigs, albino BFA strain.

Study design: in vivo (non-LLNA)

Induction
Concentration / amount:
Concentration of test material and vehicle used at induction:
Intradermal injection: 20 % test substance in olive oil -
this concentration caused irritation in a preliminary
experiment - and additionally 20 % test substance in a 1+1
mixture of olive oil and Freund's Complete Adjuvans.

Topical: 50 % test substance in vaseline (white petrolatum)
- this concentration caused irritation in a preliminary
experiment.

Concentration of test material and vehicle used for each challenge:
Topical: 0.5 % test substance in vaseline (white
petrolatum).
Challenge
Concentration / amount:
Concentration of test material and vehicle used at induction:
Intradermal injection: 20 % test substance in olive oil -
this concentration caused irritation in a preliminary
experiment - and additionally 20 % test substance in a 1+1
mixture of olive oil and Freund's Complete Adjuvans.

Topical: 50 % test substance in vaseline (white petrolatum)
- this concentration caused irritation in a preliminary
experiment.

Concentration of test material and vehicle used for each challenge:
Topical: 0.5 % test substance in vaseline (white
petrolatum).
No. of animals per dose:
Number of animals in test group: 10
Number of animals in negative control group: 5

Results and discussion

In vivo (non-LLNA)

Resultsopen allclose all
Reading:
1st reading
Hours after challenge:
24
Group:
test chemical
Dose level:
.5 %
No. with + reactions:
0
Total no. in group:
10
Remarks on result:
other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: .5 %. No with. + reactions: 0.0. Total no. in groups: 10.0.
Reading:
2nd reading
Hours after challenge:
48
Group:
test chemical
Dose level:
.5 %
No. with + reactions:
0
Total no. in group:
10
Remarks on result:
other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: .5 %. No with. + reactions: 0.0. Total no. in groups: 10.0.
Reading:
1st reading
Hours after challenge:
24
Group:
negative control
Dose level:
.5 %
No. with + reactions:
0
Total no. in group:
5
Remarks on result:
other: Reading: 1st reading. . Hours after challenge: 24.0. Group: negative control. Dose level: .5 %. No with. + reactions: 0.0. Total no. in groups: 5.0.
Reading:
2nd reading
Hours after challenge:
48
Group:
negative control
Dose level:
.5 %
No. with + reactions:
0
Total no. in group:
5
Remarks on result:
other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: negative control. Dose level: .5 %. No with. + reactions: 0.0. Total no. in groups: 5.0.

Any other information on results incl. tables

Maximum concentration not causing irritating effects in preliminary test: 1 %

Signs of irritation during induction:
Discrete grade I erythema was observed following intradermal
and topical exposure in all test animals.

Evidence of sensitisation of each challenge concentration:
No skin reactions were observed after challenge exposure.

Other observations:
No toxic signs other than local effects were observed.

Applicant's summary and conclusion

Interpretation of results:
other: not classified