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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
unknow
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1993

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
not specified
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Lithium sodium (4-((5-chloro-2-hydroxyphenyl)azo)-2,4-dihydro-5-methyl-3H-pyrazol-3-onato(2-))(3-((4,5-dihydro-3-methyl-1-(4-methylphenyl)-5-oxo-1H-pyrazol-4-yl)azo)-4-hydroxy-5-nitrobenzenesulfonato(3-)) chromate(2-)
EC Number:
414-250-7
EC Name:
Lithium sodium (4-((5-chloro-2-hydroxyphenyl)azo)-2,4-dihydro-5-methyl-3H-pyrazol-3-onato(2-))(3-((4,5-dihydro-3-methyl-1-(4-methylphenyl)-5-oxo-1H-pyrazol-4-yl)azo)-4-hydroxy-5-nitrobenzenesulfonato(3-)) chromate(2-)
Cas Number:
149564-66-9
Molecular formula:
C27H19ClCrLiN9NaO9S
Specific details on test material used for the study:
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: unknown
- Stability under storage conditions: unknown
- Stability under test conditions: unknown
- Solubility and stability of the test substance in the solvent/dispersant/vehicle/test medium: the vehicle used is water – the solubility of the test material in water is >81 g/L at 26°C and pH 7
- Reactivity of the test substance with the solvent/vehicle /test medium (if applicable): unknown
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: dilution in water
- Preliminary purification step (if any): unknown
- Preparation of a nanomaterial dispersion (incl. dilution): unknown
- Final dilution of a dissolved solid, stock liquid or gel: unknown
- Final preparation of a solid: unknown

Test animals

Species:
rabbit
Strain:
New Zealand White
Remarks:
Albino

Test system

Type of coverage:
semiocclusive
Preparation of test site:
not specified
Vehicle:
water
Controls:
not specified
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 500 mg
Duration of treatment / exposure:
4 hours
Observation period:
Not specified
Number of animals:
3 Animals
Details on study design:
OBSERVATION TIME POINTS
(indicate if minutes, hours or days)
- Erythema Score: overall at 24-48 and 72 hours
- Edema Score: overall at 24-48 and 72 hours
SCORING SYSTEM:
- Method of calculation: Draize calculation method.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
edema score
Basis:
animal #1
Time point:
24/48/72 h
Score:
0
Max. score:
1
Reversibility:
not specified
Remarks on result:
other: Max. duration: 24h; Max. value at the end of observation: 0 (related to all animals)
Irritation parameter:
edema score
Basis:
animal #2
Time point:
24/48/72 h
Score:
0
Max. score:
1
Reversibility:
not specified
Remarks on result:
other: Max. duration: 24h; Max. value at the end of observation: 0 (related to all animals)
Irritation parameter:
edema score
Basis:
animal #3
Time point:
24/48/72 h
Score:
0
Max. score:
1
Reversibility:
not specified
Remarks on result:
other: Max. duration: 24h; Max. value at the end of observation: 0 (related to all animals)
Irritant / corrosive response data:
Reversibility of any observed effect: Changes fully reversible within 1 days

Any other information on results incl. tables

Results:
- Erythema: due to the red discoloration of the skin a determination was not possible.
- Oedema: max. duration: < 24 h

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
not irritant