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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: oral
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 acute oral toxicity of the test material in rats. The rats were exposed to a dose of 2.000mg/kg bw and observed during a period of 14 days

GLP compliance:
not specified
Test type:
acute toxic class method
Limit test:
yes

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

Species:
rat
Strain:
Wistar
Sex:
female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: firma Harlan
- Weight at study initiation: ± 190g
- Housing: individual cages
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ± 3
- Humidity (%): 30-70
- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
none
Doses:
2000mg/kg bw
No. of animals per sex per dose:
4
Control animals:
yes
Details on study design:
- Duration of observation period following administration: 14 days
Statistics:
no statistics reported

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
no deaths observed
Clinical signs:
no data
Body weight:
slight increases
Gross pathology:
no data
Other findings:
none

Any other information on results incl. tables

none       

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The sample Cenizas de cinc de segunda fusion is not harmful neither toxic via the oral route
Executive summary:

This study report demonstrated no acute oral toxicity for the sample 'Cenizas de cinc de segunda fusion'