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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
review article or handbook
Title:
Final Report on the Safety Assessment of Tocopherol, TocopherylAcetate, TocopherylLinoleate, TocopherylLinoleate/Oleate, TocopherylNicotinate, TocopherylSuccinate, DioleylTocopherylMethylsilanol, Potassium Ascorbyl Tocopheryl Phosphate, Tocophersolan
Author:
Monice Zondlo Fiume
Year:
2002
Bibliographic source:
International Journal of Toxicology, 21 (Suppl. 3): 51-116, 2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
α-tocopherol
EC Number:
200-412-2
EC Name:
α-tocopherol
Cas Number:
59-02-9
Molecular formula:
C29H50O2
IUPAC Name:
(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol
Test material form:
liquid: viscous

Test animals

Species:
rabbit
Strain:
other: Japanese white

Test system

Type of coverage:
occlusive
Preparation of test site:
other: The backs of the animals were clipped free of hair 1 day prior to dosing, and the skin on the backs of four of the animals was abraded.
Vehicle:
other: 1.0% Tocopherol in "paraffinum liquidum"
Amount / concentration applied:
0.3 ml
Duration of treatment / exposure:
24 h
Observation period:
72 h
Number of animals:
8
Details on study design:
TEST SITE
- Area of exposure: The backs of the animals were clipped free of hair 1 day prior to dosing, and the skin on the backs of four of the animals was abraded. The test material, 0.3 ml, was applied to the back of each animal under an occlusive patch (using "patch-test plaster") for 24 hours. The test sites were scored for irritation 24 and 72 hours after application of the test material.

OBSERVATION TIME POINTS : 24 and 72 hours

SCORING SYSTEM:
- Method of calculation: Draize scoring system

Results and discussion

In vivo

Results
Irritation parameter:
other: primary irritation index (PII) according to Draize scoring system
Basis:
mean
Time point:
other: 24 and 72 hours
Score:
0.13
Max. score:
8
Remarks on result:
probability of weak irritation

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Tocopherol, 1.0%, was a weak primary skin irritant.