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Diss Factsheets

Toxicological information

Skin irritation / corrosion

Currently viewing:

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
other: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study
Remarks:
Test substance is equal to one component of the UVCB substance under registration and it only slightly differs from the other main identified components. Details on the read-across are available in section 13. Source study has reliability 1.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1994
Report date:
1994

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Qualifier:
according to guideline
Guideline:
EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
Reactive Red 272 - ELINCS
IUPAC Name:
Reactive Red 272 - ELINCS

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Dr. K. Thomae GmbH, Chemisch-pharmazeutische Fabrik, D-88397 Biberach
- Weight at study initiation: 2670-2810 g
- Housing: individually in metal cages
- Diet: ad libitum standard rabbit pellet - Nafag No.814, Gossau, Switzerland
- Water: drinking water, ad libitum
- Acclimation period: at least 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ± 3
- Humidity (%): 30 - 70
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Type of coverage:
semiocclusive
Preparation of test site:
shaved
Vehicle:
water
Remarks:
moistened
Controls:
no
Amount / concentration applied:
0.5 g
Duration of treatment / exposure:
4 hours
Observation period:
7 days
Number of animals:
3 male rabbits
Details on study design:
An area of at least 36 cm2 was shaved on both flanks of the animals approximately 24 hours before treatment. A gauze patch (approx. 12-16 cm2) bearing 0.5 g of test substance was applied to the right flank of each animal.
The skin area exposed directly to the test article was approx. 6 cm2. A control gauze patch was applied to the contralateral flank. Before application both patches were moistened with distilled water. The patches were loosely covered with an aluminum foil (approx. 36 cm2) and held in place for 4 hours by an adhesive tape (Isoplast, Isoplast AG, CH-5200 Brugg).
The animals were checked daily for systemic symptoms and mortality.
The skin reactions were evaluated 1, 24, 48, and 72 hours after removing the gauze patches.

SCORING SYSTEM: Draize J.H 1959
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 (beet redness) to slight eschar formation (injuries in depth)

Edema formation
0 no edema
1 very slight edema (barely perceptible)
2 slight edema (edges of area well defined by definite raising)
3 moderate edema (raised approximately 1 mm)
4 severe edema (raised more than 1 mm and extending beyond area of exposure)

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
other: 7 days
Score:
0
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 1 hour
Score:
2
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 24 hours
Score:
1.67
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 48 hours
Score:
1
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 72 hours
Score:
0.66
Max. score:
4
Irritation parameter:
edema score
Basis:
mean
Time point:
other: 7 days
Score:
0
Max. score:
4
Irritant / corrosive response data:
- Because of the red staining by the test article the evaluation of possible erythema reactions was impeded up to 72 hours after aplication in all animals. Therefore the mean values 24-72 hours for erythema reactios could not be calculated.
- Slight edema reactions were observed within 72 hours after removing the bandages.
- No signs of skin irritation was observed at the termination of the test on day 7.
Other effects:
- In 2 animals a slight loss of weight was observed on day 3 of the test.

Any other information on results incl. tables

animal no. erythema edema
445/M 497/M 491/M 445/M 497/M 491/M
1h * * * 2 2 2
24 h * * * 2 2 1
48 h * * * 1 1 1
72 h * * * 1 0 1
mean 24-72 h * * * 1.33 1 1
7 d 0 0 0 0 0 0

* erythema not evaluable, red staining

Applicant's summary and conclusion

Interpretation of results:
other: not classified according to the CLP Regulation (EC 1272/2008)
Conclusions:
Under experimental conditions, test substance was found to be not irritant or corrosive.
Executive summary:

Method

In a skin irritation study, according to OECD guideline 404, semi-occlusive application of test substance (moistened, 0.5 g) to the skin of three New Zealand White rabbits for 4 hours was done.

Results

The erythema score could not be determined due to the red color of test substance. However, after 7 days no erythema was observed. An edema score of 1.67, 1, and 0.66 was observed at 24, 48, 72 hours, respectively. Edema was fully reversible after 7 days. Under test conditions, test substance was found to be not irritating or corrosive.