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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Genetic toxicity in vitro

Description of key information
Butane-1,2-diol was not mutagenic to Salmonella typhimurium strains S. typhimurium TA 1535, TA 1537, TA 98 and TA 100 at doses up to 5,000 µg/plate with or without metabolic activation. The test substance also induced neither chromosomal aberrations nor polyploidy in Chinese hamster CHL cells at doses up to 0.9 mg/mL either with or without metabolic activation
Link to relevant study records
Reference
Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Qualifier:
according to guideline
Guideline:
JAPAN: Guidelines for Screening Mutagenicity Testing Of Chemicals
GLP compliance:
yes
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Test concentrations with justification for top dose:
Dose / Concentration: 312.5-5000 µg/ plate.
Vehicle / solvent:
DMSO
Details on test system and experimental conditions:
Exposure comments:
Doses of: 0, 312.5, 625, 1250, 2500 or 5000 micrograms of 1,2-butanediol were applied per plate in 3 plates.
Positive control:
A) S9 negative received AF-2 sodium azide or 9-aminoacridine
B) S9 positive received 2-aminoanthracene. S9 activated by phenobarbital and 5,6-benzoflavone.
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
negative

Minimum concentration of test substance at which toxicity to bacteria was observed is > 5000ug/plate with metabolic activation and 5000ug/plate without metabolic activation.

In all strains at all concentrations tested, with or without metabolic activation, the test substance did not induce any changes within the chromosomal chromatin.

Executive summary:

CAS 584-03-2 was considered as "negative" in gene mutation tests under the experimental conditions used.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

Justification for classification or non-classification