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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity: in vitro

Currently viewing:

Administrative data

Endpoint:
in vitro cytogenicity / chromosome aberration study in mammalian cells
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
The EU RAR (2005) reports the findings of a number of published tests of cytogenicity / clastogenicity performed with Cr (VI) compounds and incorporates the findings of previous reviews by the UK Health & Safety Executive (HSE; 1989) and the UK Institute of Occupational Health (IOH, 1997). Individual studies are of varying reliability but the overall conclusion (weight of evidence) is considered to be reliable.
Cross-reference
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
other: review
Title:
European Union Risk Assessment Report: chromium trioxide, sodium chromate, sodium dichromate, ammonium dichromate and potassium dichromate
Author:
European Chemicals Bureau
Year:
2005
Bibliographic source:
3rd. Priority List; Volume 53

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Cytogenicity Study
Principles of method if other than guideline:
The EU RAR summarises the findings of a number of cytogenicity studies performed to various non-standard designs.
GLP compliance:
no
Remarks:
largely older, literature studies
Type of assay:
in vitro mammalian chromosome aberration test

Test material

Constituent 1
Chemical structure
Reference substance name:
Chromium trioxide
EC Number:
215-607-8
EC Name:
Chromium trioxide
Cas Number:
1333-82-0
Molecular formula:
CrO3
IUPAC Name:
Trioxochromium
Constituent 2
Chemical structure
Reference substance name:
Sodium dichromate
EC Number:
234-190-3
EC Name:
Sodium dichromate
Cas Number:
10588-01-9
Molecular formula:
Cr2Na2O7
IUPAC Name:
sodium dichromate
Constituent 3
Chemical structure
Reference substance name:
Sodium chromate
EC Number:
231-889-5
EC Name:
Sodium chromate
Cas Number:
7775-11-3
Molecular formula:
CrH2O4.2Na
IUPAC Name:
disodium dioxido(dioxo)chromium
Constituent 4
Chemical structure
Reference substance name:
Potassium dichromate
EC Number:
231-906-6
EC Name:
Potassium dichromate
Cas Number:
7778-50-9
Molecular formula:
Cr2H2O7.2K
IUPAC Name:
potassium dichromate
Details on test material:
No further details are reported

Method

Target gene:
Not applicable - cytogenicity / clastogenicity assays
Species / strain
Species / strain / cell type:
other: various
Metabolic activation:
with and without
Metabolic activation system:
various
Test concentrations with justification for top dose:
Various
Vehicle / solvent:
Not reported for individual studies
Controls
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
not specified
True negative controls:
not specified
Positive controls:
not specified
Positive control substance:
not specified
Details on test system and experimental conditions:
Not reported for individual studies
Evaluation criteria:
Not reported for individual studies
Statistics:
Not reported for individual studies

Results and discussion

Test results
Species / strain:
other: various
Metabolic activation:
with and without
Genotoxicity:
positive
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified
Additional information on results:
The results of in vitro cytogenicity /clastogenicity / chromosomal aberration tests performed with the water-soluble Cr (VI) compounds in this group are invariably positive.
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

The results of in vitro cytogenicity /clastogenicity / chromosomal aberration tests performed with the water-soluble Cr (VI) compounds in this group are invariably positive.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
positive weight of evidence

The results of numerous tests performed with water-soluble Cr (VI) compounds indicate that this group of compounds is clastogenic in vitro.
Executive summary:

There is a very large body of evidence indicating that the Cr (VI) ion in solution is directly clastogenic in vitro. This activity was diminished considerably by the presence of reducing agents, in the form of tissue S9 or S12 fractions, gastric juice or reducing agents such as glutathione, ascorbate or sulphite. These all serve to reduce Cr (VI) to Cr (III) outside the cell therefore greatly reducing entry of chromium into the cell.