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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
in vivo mammalian cell study: DNA damage and/or repair
Type of information:
experimental study planned
Justification for type of information:
CONSIDERATIONS OF ALTERNATIVE METHODS ON TESTING PROPOSALS IN YOUR REGISTRATION

Public substance name: Tris(2-hydroxyethyl) isocyanurate triacrylate
EC Number: 254-843-6
CAS Number: 40220-08-4

Date of considerations: 21 December 2018

Hazard endpoint for which vertebrate testing was proposed:
In vivo mammalian alkaline comet assay (test method: OECD TG 489)

Considerations that the general adaptation possibilities of Annex XI of the REACH Regulation were not adequate to generate the necessary information

• available GLP studies
None.

• available non-GLP studies
None.

• historical human data
None.

• (Q)SAR
No reliable QSAR model is available to replace the in vivo Comet assay in rodents.

• in vitro methods
In vitro study (Ames test) has already performed on Tris(2-hydroxyethyl) isocyanurate triacrylate. As the results is positive, an in vivo study is required to evaluate the relevance of the in vitro positive results.

• weight of evidence
No data is available which allow a weight of evidence approach.

• grouping and read-across
None

• substance-tailored exposure driven testing [if applicable]
Not applicable

• [approaches in addition to above [if applicable]
Not applicable

• other reasons [if applicable]
None


Considerations that the specific adaptation possibilities of Annexes VI to X (and column 2 thereof) were not applicable:

Test proposal is fully compliant with ECHA guidance R 7.a (2017, page 575).
No specific adaptation possibilities of Annexes VI to X (and column 2 thereof) are applicable.

According to the OECD guidance R7A, when an Ames test was positive, an in vivo study could be proposed instead of launching both in vitro tests on mammalian cells. Indeed, with one positive in vitro test, an in vivo study is required in the REACH regulation. The in vivo alkaline comet assay (OECD 489) recognises primary DNA damage that would lead to gene mutations and/or chromosome aberrations, but will also detect DNA damage that may be effectively repaired or lead to cell death. The comet assay can be applied to almost every tissue of an animal from which single cell or nuclei suspensions can be made, including specific site of contact tissues.

Data source

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 489 (In vivo Mammalian Alkaline Comet Assay)

Test material

1
Chemical structure
Reference substance name:
(2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl triacrylate
EC Number:
254-843-6
EC Name:
(2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl triacrylate
Cas Number:
40220-08-4
Molecular formula:
C18H21N3O9
IUPAC Name:
(2,4,6-trioxo-1,3,5-triazinane-1,3,5-triyl)triethane-2,1-diyl trisacrylate

Results and discussion

Applicant's summary and conclusion