Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 201-855-4 | CAS number: 88-74-4
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- methaemoglobinaemia
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Old study, but correctly discribed and important in MetHb induction comparing animals and human, and isomers for induction. Publication in french, only summary in english.
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Action Methemoglobinisante de Dérivés Trifluorométhyles de la Phenyl-3 Oxazolidinone-2.
- Author:
- Sergant M, Gouret C, Raynaud G, Delatte G
- Year:
- 1 969
- Bibliographic source:
- Proc. Eur. Soc. Study Drug Toxicity Vol. 11, pp. 212-221.
- Reference Type:
- secondary source
- Title:
- SIDS Initial Assessment Report for SIAM 13 (o-nitroaniline) November 6-9, 2001 Bern, Final July 2003.
- Author:
- OECD SIDS
- Year:
- 2 003
- Bibliographic source:
- UNEP Publications
Materials and methods
- Principles of method if other than guideline:
- The production of methemoglobin was studied in dogs with aniline, and p-,m-, and o-trifluoromethylaniline. The products were administered twice at 24-hour intervals. The levels of methemoglobin and sulfhemoglobin were measured 24 hours after the second administration.
- GLP compliance:
- no
- Type of method:
- in vivo
- Endpoint addressed:
- repeated dose toxicity: oral
Test material
- Reference substance name:
- ortho-trifluoromethyl-aniline
- IUPAC Name:
- ortho-trifluoromethyl-aniline
- Details on test material:
- no data
Constituent 1
Test animals
- Species:
- dog
- Strain:
- other: bastard
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: capsule
- Vehicle:
- not specified
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 2 oral administrations at 24 h intervals
- Frequency of treatment:
- two times
- Post exposure period:
- 72 hours
Doses / concentrations
- Remarks:
- Doses / Concentrations:
27.5, 55, and 110 mg/kg bw
Basis:
actual ingested
- No. of animals per sex per dose:
- no data
- Control animals:
- yes
Examinations
- Examinations:
- Blood was taken by punction of the cephalic vein adding heparin before administration of the products and 24 hr after the last administration.
MetHemoglobin (MetHb) and SulfHemoglobin (SHb) determination was conducted according to described methods (Evelyn & Malloy 1938, De Traverse et al 1961). MetHb was transformed in CyanHb and optical density difference was measured by suppressing the characteristic absorption of Hb at 635 μm. SulfHb was measured by residual optical density at 620 μm after conversion of Hb and MetHb in CyanHb. Total Hb was measured with Rabkin reagent following the method described by Crosby et al. (1957).
Evelyn & Malloy (1938). J. biol. Chem. 126: 655
De Traverse et al. (1961). Ann. Biol. Clin. 3-4: 303
Crosby et al. (1957). Blood 12: 1132
Results and discussion
Any other information on results incl. tables
The trifluoromethyl-aniline isomers (o-m-p TFMA) were used at 110, 55 or 27.5 mg/kg bw and aniline at doses of 15, 30, and 100 mg/kg bw in dogs, respectively.
After the first administration of para-TFMA, a rapid rise in MehHB (50% at 1h30) was observed in the test animal and the animal died within hours. Then the other isomers were only administered at 2 x 55 mg/kg bw. At this dose MetHb was: para-TFMA: 50%; meta-TFMA: 30%; ortho-TFMA: 1%.
Administration of aniline at 2 x 100 mg/kg bw resulted in 50% MetHb.
Thus, para-TFMA was a more potent MetHb inducer than aniline, while meta-TFMA was a weaker inducer and ortho-TFMA not inducing.
Applicant's summary and conclusion
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.