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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
in vitro gene mutation study in mammalian cells
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1986
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The test was conducted with the familiar mammalian cell and with positive control and solvent control.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1988

Materials and methods

Test guideline
Qualifier:
no guideline available
Guideline:
other:
Deviations:
not specified
Principles of method if other than guideline:
The methodology was not reported.
GLP compliance:
no
Type of assay:
mammalian cell gene mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Hydroxylammonium chloride
EC Number:
226-798-2
EC Name:
Hydroxylammonium chloride
Cas Number:
5470-11-1
Molecular formula:
ClH.H3NO
IUPAC Name:
hydroxyammonium chloride
Test material form:
not specified
Details on test material:
Name: Hydroxylamine HCI

Method

Target gene:
L5178Y Mouse Lymphoma Cell
Test concentrations with justification for top dose:
No data
Evaluation criteria:
No data
Statistics:
No data

Results and discussion

Test results
Species / strain:
mouse lymphoma L5178Y cells
Metabolic activation:
not specified
Genotoxicity:
positive
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
positive

Hydroxylamine HCI induced mutagenic response in the mouse lymphoma cell mutagenesis assay. Thus, it is considered mutagenic.