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EC number: 209-057-8 | CAS number: 554-00-7
- 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
Additional information on environmental fate and behaviour
Administrative data
- Endpoint:
- additional information on environmental fate and behaviour
- Type of information:
- other: BUA report
- Adequacy of study:
- other information
- Reliability:
- other: BUA report
- Rationale for reliability incl. deficiencies:
- other: No reliability is given as this is a summary entry for the BUA report.
Data source
Referenceopen allclose all
- Reference Type:
- secondary source
- Title:
- 2,4-Dichloranilin; 2,5-Dichloranilin; 3,4-Dichloranilin
- Author:
- Beratergremium für umweltrelevante Altstoffe (BUA)
- Year:
- 1 994
- Bibliographic source:
- Wissenschaftliche Verlagsgesellschaft, BUA report 140
- Reference Type:
- publication
- Title:
- Pesticide transformations: production of chloroazobenzenes from chloroanilines
- Author:
- Bartha R, Linke HAB, Pramer D
- Year:
- 1 968
- Bibliographic source:
- Science 161, 582-583
- Reference Type:
- publication
- Title:
- Biochemical transformations of herbicide-derived anilines: requirements of molecular configuration.
- Author:
- Bordeleau LM and Bartha R
- Year:
- 1 972
- Bibliographic source:
- Can. J. Microbiol. 18, 1873 ¿ 1882
Materials and methods
- Principles of method if other than guideline:
- BUA report
- GLP compliance:
- no
Test material
- Reference substance name:
- 2,4-dichloroaniline
- EC Number:
- 209-057-8
- EC Name:
- 2,4-dichloroaniline
- Cas Number:
- 554-00-7
- Molecular formula:
- C6H5Cl2N
- IUPAC Name:
- 2,4-dichloroaniline
Constituent 1
Results and discussion
Any other information on results incl. tables
Biotransformation in soil to higher molecular weight compounds
Bordeleau and Bartha, 1972
The authors suggest that the formation of trichloroaniline in soil is catalyzed by peroxidases. In a study two enzymes, a peroxidase and an anilineoxidase, of the fungus Geotrichum candidum L-3, were tested ¿in vitro¿ for their ability to transform dichloroanilines with the help of H2O2 into higher molecular weight compounds. The peroxidase was able to transform 2,4 -, 2,5 - and 3,4-dichloroaniline into their corresponding tetrachloro-azo-compound. The anilineoxidase transformed 2,4-dichloroaniline to 2,2 '4, 4'-tetrachloroazobenzene.
Bartha et al., 1968
"Nixon soil" (pH 5.5) was mixed with 1000 mg of 2,4-dichloroaniline/kg soil (dry weight and set to 60% of its field capacity. No tetrachlorobenzene was found after 16 days of incubation at 27 °C. However other unspecified azo-compounds could be identified.
Applicant's summary and conclusion
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