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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
skin corrosion: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2018
Report date:
2018

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Bis(pentane-2,4-dionato-O,O')magnesium
EC Number:
237-857-7
EC Name:
Bis(pentane-2,4-dionato-O,O')magnesium
Cas Number:
14024-56-7
Molecular formula:
C10H14MgO4
IUPAC Name:
magnesium;4-oxopent-2-en-2-olate
Test material form:
solid: particulate/powder

In vitro test system

Test system:
human skin model
Source species:
human
Cell type:
non-transformed keratinocytes
Cell source:
foreskin from multiple donors
Vehicle:
unchanged (no vehicle)
Control samples:
yes, concurrent negative control
yes, concurrent positive control
Amount/concentration applied:
The test item, Magnesium Acetylacetonate/N56, was a white powder. A nominal weight of 25 mg of the test item was applied to the tissue, previously wetted with 25 μL water (and spread over the surface of the tissue if required). A 25 mg application spoon (sharp spoon, NaCl weight 25 ~ 1 mg) was used to dispense the test item. A levelled spoonful of test item was weighed prior to the test to confirm the weight of the volume used.
The controls were in liquid form. A volume of 50 μL was dispensed over each tissue using a suitable pipette.
Duration of treatment / exposure:
Duplicate tissues were dosed for three minutes and duplicate tissues dosed for one hour with test item, negative control or positive control.
Number of replicates:
2 with 3 minutes contact
2 with 1 hour contact

Results and discussion

In vitro

Resultsopen allclose all
Irritation / corrosion parameter:
% tissue viability
Run / experiment:
1 (3 minutes contact)
Value:
ca. 105.1
Vehicle controls validity:
valid
Negative controls validity:
not applicable
Positive controls validity:
valid
Remarks on result:
no indication of irritation
Irritation / corrosion parameter:
% tissue viability
Run / experiment:
2 (1 hour contact)
Value:
ca. 106.4
Vehicle controls validity:
valid
Negative controls validity:
not applicable
Positive controls validity:
valid
Remarks on result:
no indication of irritation

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Executive summary:

The skin corrosion study was performed according to the OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method).

The test item was considered as non corrosive to the skin.