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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
April 2007 - May 2007
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP-guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2007
Report date:
2007

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
1,1'-(1,3-Phenylenedicarbonyl)diazepan-2-one
EC Number:
616-020-3
Cas Number:
7381-13-7
Molecular formula:
C20H24N2O4
IUPAC Name:
1,1'-(1,3-Phenylenedicarbonyl)diazepan-2-one
Details on test material:
none

Test animals

Species:
rabbit
Strain:
other: New Zealand
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Elevage de Gerome (Quartier Labaste - F40260 Linxe)
- Weight during the test: 2.23 kg .- 2.92 kg
- Housing: Each animal was kept in an individual box installed in conventional air conditioned animal husbanding.
- Acclimation period: 5-day

ENVIRONMENTAL CONDITIONS
- Temperature (°C): between 19°C and 22°C
- Humidity (%): between 40% and 70%
- conventional air conditioned

Test system

Type of coverage:
semiocclusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): dose of 0.5 g

Duration of treatment / exposure:
4 hours
Observation period:
The skin reactions were appreciated I hour and then 24, 48 and 72 hours after removal of the patch.
If no reaction is observed 72 hours after the treatment the study is terminated
Number of animals:
3 female rabbits
Details on study design:
TEST SITE
- Area of exposure: on an undamaged skin area of one flank of each animal
- Type of wrap if used: strip of surgieal adhesive tape.

REMOVAL OF TEST SUBSTANCE
- Washing (if done): rinsing with distilled water
- Time after start of exposure:

SCORING SYSTEM:

Erythema and Eschar formation:
0 ...... No erythema
1 ...... Very slight erythema (barely perceptible)
2 ...... Well defined erythema
3 ...... Moderate to severe erythema
4 ... ... Severe erythema (beef redness) with eschars formation preventing grading of erythema

Oedema:
0 ....... No oedema
1 ....... Very slight oedema (barely perceptible)
2 ....... Slight oedema (contour clearly defined)
3 ....... Moderate oedema (raised approx. 1 mm)
4 ...... Severe oedema (raised more than 1mm, and extending beyond area of exposure)

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
other: Erythema and eschar
Basis:
animal: #1,#2,#3
Time point:
other: 1,24,48,72 hours
Score:
0
Max. score:
4
Reversibility:
other: No cutaneous reactions
Irritation parameter:
edema score
Basis:
animal: #1,#2,#3
Time point:
other: 1,24,48,72 hours
Score:
0
Max. score:
4
Reversibility:
other: No cutaneous reactions
Irritant / corrosive response data:
- Raw data for each individual animal at each observation time up to removal of each animal from the test: data are given in above block of fields
'Irritation / corrosion results'.
Other effects:
none

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
not to be classified
Executive summary:

The test item was applied, as supplied, at the dose of 0.5 g, under semi-occlusive dressing

during 4 hours on an undamaged skin area of three New Zealand rabbits.

No cutaneous reactions (el)'thema and oedema) were observed whatever the examination time (1, 24, 48 and 72 hours).