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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
not applicable
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Well documented and scientifically good . Not according to GLP nor to specific test guidelines.
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2009
Report date:
2009

Materials and methods

Principles of method if other than guideline:
A study was conducted to evaluate the eye irritation of the test material in rabbits. The rabbits were exposed to a dose of 2.000mg/kg bw and observed during a period of 14 days
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Residues, zinc smelting
EC Number:
273-824-3
EC Name:
Residues, zinc smelting
Cas Number:
69029-83-0
Molecular formula:
Not available, UVCB substance.
IUPAC Name:
Residues, zinc melting, alloying and casting
Details on test material:
name of test substance: Cenizas de cinc de segunda fusion
origin of test substance: Befesa Zinc Amorebieta

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: firma Harlan
- Housing: individual cages
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ± 2
- Humidity (%): 30-70
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Vehicle:
unchanged (no vehicle)
Controls:
yes, concurrent no treatment
Amount / concentration applied:
no information
Duration of treatment / exposure:
up to 72 hours
Observation period (in vivo):
24, 48 and 72 hours
Number of animals or in vitro replicates:
no information
Details on study design:
none

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
other: 24, 48, 72h
Score:
0
Max. score:
4
Reversibility:
not specified
Irritation parameter:
iris score
Basis:
mean
Time point:
other: 24, 48, 72h
Score:
0
Max. score:
2
Reversibility:
not specified
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
other: 24, 48, 72h
Score:
0
Max. score:
3
Reversibility:
not specified
Irritation parameter:
chemosis score
Basis:
mean
Time point:
other: 24, 48, 72h
Score:
0
Max. score:
4
Reversibility:
not specified
Irritant / corrosive response data:
none
Other effects:
none

Any other information on results incl. tables

none

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
This study reported that the test material is not an eye irritant
Executive summary:

This study reported that the test material is not an eye irritant