Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute Toxicity: dermal

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
calculation (if not (Q)SAR)
Remarks:
estimated by calculation
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Automatic calculation with MeClas tool
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:
other: software
Title:
Unnamed
Year:
2014

Materials and methods

Principles of method if other than guideline:
Acute dermal toxicity potential of the UVCB substance was determined by classifying based on the Mixture rules from EU CLP (additivity formula of classified components to derive hazard class) and back calculation to the corresponding acute toxicity range estimate.
GLP compliance:
no
Remarks:
other quality assurance was applied

Test material

Constituent 1
Reference substance name:
aluminium, magnesium and silicon oxides and hydroxides from refinement of aluminium salt slag residues
Molecular formula:
UVCB
IUPAC Name:
aluminium, magnesium and silicon oxides and hydroxides from refinement of aluminium salt slag residues
Test material form:
solid: particulate/powder

Results and discussion

Effect levels
Dose descriptor:
other: acute toxicity estimate ATE
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Remarks on result:
other: prediction

Any other information on results incl. tables

According to MeClas, the substance is not classified as Acute toxicity Dermal under CLP.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Good quality, conservative estimate of the Acute Dermal Toxicity Estimate of the UVCB substance.
The substance is not classified as acute toxic - dermal.
Executive summary:

The study provided a conservative estimate, derived on basis of the classification outcome (mixture toxicity rules) from a reasonable worst-case substance representative. 


 


Validity of the model used:



  1. Defined endpoint: the endpoint is a REACH compliant defined endpoint

  2. Unambiguous algorithm: EU CLP guidance based summation formula to determine classification, followed by back-calculation to related hazard criteria

  3. Applicability domain: applicable to classify complex metal containing materials. 

  4. Mechanistic interpretation - metal species: the tool translates the elemental composition into a mineralogical composition relevant for classification.