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EC number: 203-583-1 | CAS number: 108-44-1
- 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
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- Endpoint summary
- Stability
- Biodegradation
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- 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

Additional toxicological data
Administrative data
- Endpoint:
- additional toxicological information
- Adequacy of study:
- other information
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Toxicodynamic properties of toluidines in chronic poisoning Part 1 Experiments on animals maintained on protein-rich diet
- Author:
- Malik-Brys, M., Senczuk, W.,
- Year:
- 1 995
- Bibliographic source:
- Bromatologia I Chemia|Toksykologiczna 28, 67-71
- Reference Type:
- publication
- Title:
- Toxicodynamic properties of toluidines in chronic poisoning Part II Tests on animals maintained on low-protein diet
- Author:
- Malik-Byrs M, Senczuk W
- Year:
- 1 995
- Bibliographic source:
- Bromatologia I Chemia|Toksykologiczna 28, 175-178
Materials and methods
- Type of study / information:
- Type: other: toxicodynamic properties in chronic poisoning
Test material
- Reference substance name:
- m-toluidine
- EC Number:
- 203-583-1
- EC Name:
- m-toluidine
- Cas Number:
- 108-44-1
- Molecular formula:
- C7H9N
- IUPAC Name:
- 3-methylaniline
Constituent 1
Results and discussion
Any other information on results incl. tables
Aim of study was to assess delayed toxic effects of toluidine isomers during prolonged exposure in female Wistar rats.
1) Isomers were added to food containing 24% protein. Within the dose and exposure-duration range used, o-toluidine reached highest blood and urine concentration
2) Toluidines were added to food containing 8% protein. Within the ranges of doses and exposure times used in the experimentsthe highest blood and urine concentrations were recorded for o-toluidine and the lowest for p-toluidine (from english abstract of polish paper).
Applicant's summary and conclusion
- Conclusions:
- Aim of study was to assess delayed toxic effects of toluidine isomers during prolonged exposure in female Wistar rats.
1) Isomers were added to food containing 24% protein. Within the dose and exposure-duration range used, o-toluidine reached highest blood and urine concentration
2) Toluidines were added to food containing 8% protein. Within the ranges of doses and exposure times used in the experimentsthe highest blood and urine concentrations were recorded for o-toluidine and the lowest for p-toluidine (from english abstract of polish paper).
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