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EC number: 407-550-4 | CAS number: 69184-17-4
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
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Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Table 1: Summary of genotoxicity studies with Fluroxypyr acid
Test system |
Test object |
Conc. of Fluroxypyr* |
Batch and purity of Fluroxypyr |
Positive controls |
Results |
Reference |
Ames |
S. typhimuriumTA 98, 100, 1535, 1537 and 1538 |
10 - 10,000 |
Lot 140-75-8 |
-naphthyl-amine, |
Negative |
Hossack et al., 1979 |
In vitro CHO chromosome aberration |
Chinese hamster ovary cells |
62.5 - 1000 |
Lot 433T-1282-7 |
CPA, |
Negative |
Holmstrom & Mc Gregor, 1983a |
In vitro unscheduled DNA synthesis |
Human embryonic lung cells |
1 - 4000 |
Lot 433T-1282-7 |
EMS |
Negative |
Mc Gregor & Riach, 1983a |
In vitro CHO/ HGPRT |
Chinese hamster ovary cells (CHO-K1, CCL 61) |
500 - 2000 |
Lot433T-1282-7 |
EMS, |
Negative |
Davis, 1983 |
In vitro |
L5178Y with heterozygous, TK locus |
33.3 - 3333.3 |
Lot 433T-1282-7 |
EMS, |
Positive |
Mc Gregor & Riach, 1983b |
In vivo chromosome aberration in Chinese hamsters |
Femoral bone marrow cells |
Five daily gavage doses of 73 - 735 mg/kg |
Lot 433T-1282-7 |
CPA |
Negative |
Holmstrom & Mc Gregor, 1983a |
* The carrier was DMSO in all in vitro tests and 0.5% aqueous SCMC in the in vivo test
The only positive result obtained with Fluroxypyr acid was mutation of the thymidine kinase (TK) locus from the heterozygous TK+/- to the homozygous TK-/- condition in in vitro cultured L5178Y mouse lymphoma cells. In accordance with the evaluation criteria specified in the report, results did not indicate a significant response although the mutation frequency at the highest valid concentration of 1000 µg/ml was marginally increased (<2-fold) in the presence of S9 metabolic activation. These data indicated that any potential unequivocal response would only occur between 1000 and 3000 µg/ml; the second phase therefore employed concentrations in the range 800 - 2400 µg/ml. Results indicated weak mutagenic responses in both the presence and absence of S9-mix. The positive results were subsequently reproduced in another independent investigation, which also looked at the effect of pH on the response, as pH and osmolality changes are known to produce positive results in this type of assay. These results showed that the mutagenic activity of Fluroxypyr could be substantially reduced by maintaining pH around neutrality during the exposure period suggesting that activity is due to an ionised form of Fluroxypyr or its interaction with the test medium.
Short description of key information:
see Discussion
Endpoint Conclusion:
Justification for classification or non-classification
In conclusion, a positive result was obtained in one of five in vitro mutagenicity tests. It is likely that this represents a false positive result. All other tests, including those that, like the mouse lymphoma test, are capable of detecting point mutations, were negative. In addition, as indicated in the next section of this document 7.7. Fluroxypyr is not carcinogenic in animals at toxic and limit dosages.
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