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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1997

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3,10-bis[(2-aminopropyl)amino]-6,13-dichloro-5,12-dioxa-7,14-diazapentacene-4,11-disulfonic acid
EC Number:
692-514-2
Cas Number:
133047-57-1
Molecular formula:
C24H24Cl2N6O8S2
IUPAC Name:
3,10-bis[(2-aminopropyl)amino]-6,13-dichloro-5,12-dioxa-7,14-diazapentacene-4,11-disulfonic acid

Test animals

Species:
rabbit
Strain:
New Zealand White

Test system

Number of animals:
1 male and 2 females
Details on study design:
The primary skin irritation potential of the test article was investigated by topical application
of 0.5 g to 6 cm2 intact dorsal skin of each of three young adult New Zealand rabbits. The
scoring of skin reactions was performed 1, 24, 48 and 72 hours after removal of the dressing.
The scores of each animal at the following reading times (24, 48, 72 hours) were used in
calculating the respective mean values for each type of lesion.

Results and discussion

Any other information on results incl. tables

RESULTS

VIABILITY/MORTALITY AND CLINICAL SIGNS

No clinical signs of systemic toxicity were observed in the animals during the test and

observation period, and no mortality occurred.

IRRITATION

Application of the test article to healthy intact rabbit skin resulted in a primary irritation score

of 0.00.

Local signs (mean values from 24 to 72 hours) consisted of grade 0.00 erythema and grade

0.00 edema.

COLORATION

Light violet or violet staining by the test article of the treated skin was observed.

CORROSION

No irreversible alterations of the treated skin were observed nor were corrosive effects

evident on the skin.

Applicant's summary and conclusion

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

not irritating