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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: No deviation from OECD-404 guideline, GLP.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2005

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Remarks:
GLP Certificate as an annexe in the study report.

Test material

Constituent 1
Reference substance name:
-
EC Number:
483-960-7
EC Name:
-
IUPAC Name:
D-pentose and D-glucose, oligomeric, C8 and C10 alkyl glycosides

Test animals

Species:
rabbit
Strain:
New Zealand White

Test system

Type of coverage:
semiocclusive
Preparation of test site:
abraded
Vehicle:
unchanged (no vehicle)
Controls:
yes
Duration of treatment / exposure:
72h
Observation period:
1, 24, 48 and 72 hours.
Number of animals:
3 animals per dose
Details on study design:
The test product was applied, after being heated at 80°C, at a dose of 0.5 ml/L, on an undamaded skin area of the right flank of the animal. On the left flank an untreated area was served as the control.

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 72h
Score:
ca. 0
Max. score:
0
Reversibility:
other: not relevant as no effect
Remarks on result:
other: no erythema & eschar, no oedema at all time points of the study

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
No erythema & eschar, no oedema at all time points of the study, primary irritation score is 0.0. It can be concluded that APP-6781 is not irritant to skin and that no classification is needed for this endpoint.
Executive summary:

The susbtance APP-6781 (TA 8/10) was applied, after being heated, under semi-occlusive dressing during 4 hours on an undameded skin area of three New Zealand rabbits at the dose of 0.5 ml, according to OECD-404 guideline. No cutaneous reactions, erythema and oedema, were observed whatever the examination time. Results enabled to conclude that the substance is not a skin irritant and doesn't need any classification for this endpoint.