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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
Study period:
1994-05-05 - 1994-06-30
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The GLP study was conducted according to an internationally accepted guideline (OECD 404). All study parameters are based on the specific guideline.

Data source

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

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
1,3,5-Triazine-2,4,6-triamine, deammoniated
EC Number:
272-034-6
EC Name:
1,3,5-Triazine-2,4,6-triamine, deammoniated
Cas Number:
68649-66-1
Molecular formula:
see structural formula below
IUPAC Name:
1,3,5-Triazine-2,4,6-triamine, deammoniated

Test animals

Species:
rabbit
Strain:
other: White russian (Albino)

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
water
Controls:
not required
Amount / concentration applied:
0.5 g
Duration of treatment / exposure:
4 hours
Observation period:
3 days
Number of animals:
2 males, 1 female
Details on study design:
One day before treatment the dorsal skin area between shoulder and sacrum was clipped free of hair. To ensure a tight contact with the skin 0.5 g of the test substance was grinded in a ball mill and moistened with 0.5 ml demineralized water and was given on the left site of the vertebral column. The site of application was covered with a patch (6.25 cm2).
The opposite area of the dorsal skin was treated in the same way but without test substance (control site). A bandage wrapped several times around the trunk (Acrylastic, No. 2408, width 8 cm; supplied by P. Beiersdorf and Co.AG, D-20245 Hamburg) provided a complete occlusion. After the end of the exposition time remaining test material was gently washed off as far as possible.
The treated skin area was assessed qualitatively (erythema/eschar resp. edema) and quantitatively (values 0 - 4) using the Draize method (1, 2, 4, 5). In addition, attention was paid to the occurrence of further reactions on the skin (e.g. corrosive effects) and to clinical symptoms (systemic toxic effects).

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 72 hours
Score:
0
Max. score:
8
Reversibility:
no data
Irritation parameter:
erythema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
not specified
Irritation parameter:
edema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
not specified

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Durferrit REG 1 was tested for skin corrosive/irritating properties on the skin of rabbits. Neither erythema nor edema could be detected. REG 1 is non-irritant to the skin of rabbits.
Executive summary:

Durferrit REG 1 was tested for skin corrosive/irritating properties on the skin of rabbits. Neither erythema nor edema could be detected. REG 1 is non-irritant to the skin of rabbits.