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EC number: 202-429-0 | CAS number: 95-53-4
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1979
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 979
- Report date:
- 1979
- Reference Type:
- publication
- Title:
- o-TOLUIDINE CAS No: 95-53-4 SIDS Initial Assessment Report.
- Author:
- OECD SIDS
- Year:
- 2 006
- Bibliographic source:
- UNEP Publications
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Draize Test according Fed. Reg, 38, No,187, §1500.41, p. 27029 (1973/sept./ 27)
- Principles of method if other than guideline:
- Draize Test according Fed. Reg, 38, No,187, §1500.41, p. 27029 (1973/sept./ 27)
- GLP compliance:
- no
- Remarks:
- GLP was not mandatory at the time of the study
Test material
- Reference substance name:
- o-toluidine
- EC Number:
- 202-429-0
- EC Name:
- o-toluidine
- Cas Number:
- 95-53-4
- Molecular formula:
- C7H9N
- IUPAC Name:
- 2-methylaniline
- Test material form:
- other: liquid
- Details on test material:
- - Name of test material (as cited in study report): o-toluidine
- Analytical purity: 99.5%
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Gaukler, Germany
- Age at study initiation: male: 3.1kg, 2.88kg, 2.71kg; female: 2.94 kg, 2.79kg, 3.17kg
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- Undiluted o-Toluidine was applied on a cotton pad (2.5cmx2.5cm) for application on the skin
- Duration of treatment / exposure:
- 24 hour(s)
- Observation period:
- After application of patch: 24h, 48h, 72h and 7 days and 8 days
- Number of animals:
- 6
- Details on study design:
- Each animal received two applications of the test material. One on the intact skin of the right flank and the other one on the scarified skin of the left flank. 24h, post application, the skin of the animals were washed with water. The assessment of the dermal changes was based on the OECD Draize scoring method. Moreover, the animals were observed for mortality and clinical signs of toxicity
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- other: 24h, 48h, 72h
- Score:
- ca. 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 1.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks:
- with 8 days
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 1.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 1.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 1.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- other: 24h, 48h, 72h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- other: 24h, 48h, 72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks:
- within 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- other: 24h, 48h, 72h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #5
- Time point:
- other: 24h, 48h, 72h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks:
- within 8 days
- Irritation parameter:
- edema score
- Basis:
- animal #6
- Time point:
- other: 24h, 48h, 72h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 8 days
- Irritant / corrosive response data:
- The treatment led to slight or moderate erythema and moderate edema in 5/6 animals up to 72h and 24h after start of the application, respectively. At 72 h after application, the same five animals exhibited scaling, which persisted till day 8 of the study. Necrosis (soft, parchment like or leathery) was observed in one animal till the termination of the study. The clinical finding of the necrosis was confirmed by macroscopic pathology.
- Other effects:
- Systematic Toxicity: No mortality occurred. There were no clinical signs of systemic toxicity from the dermal exposure
Any other information on results incl. tables
Scoring Method used: OECD Draize scores
Time (hrs) |
Individual scoring |
||||||
Animal 1 |
Animal 2 |
Animal 3 |
Animal 4 |
Animal 5 |
Animal 6 |
||
Erythema |
|||||||
24 h |
2 |
2 |
4 |
2 |
2 |
2 |
|
48 h |
2 |
2 |
4 |
2 |
2 |
2 |
|
72 h |
2 |
1 |
4 |
1 |
1 |
1 |
|
mean |
2 |
1.66 |
4 |
1.66 |
1.66 |
1.66 |
|
Edema |
|||||||
24 h |
2 |
2 |
2 |
2 |
2 |
2 |
|
48 h |
2 |
2 |
2 |
2 |
2 |
2 |
|
72 h |
0 |
0 |
2* |
0 |
0 |
0 |
|
mean |
1.33 |
1.33 |
2 |
1.33 |
1.33 |
1.33 |
Time (hrs) |
Individual scoring |
||||||||||||
Animal 1 |
Animal 2 |
Animal 3 |
Animal 4 |
Animal 5 |
Animal 6 |
||||||||
Erythema |
|
||||||||||||
8 days |
0 |
0 |
4 |
0 |
0 |
0 |
|
||||||
Edema |
|
||||||||||||
8 days |
0 |
0 |
2* |
0 |
0 |
0 |
|
*= signs extends beyond the area of exposure
Applicant's summary and conclusion
- Interpretation of results:
- Category 2 (irritant)
- Remarks:
- Migrated information Criteria used for interpretation of results: other: EU-GHS-CLP
- Executive summary:
BASF (1979)
Undiluted o-toluidine was applied to the intact and to the scarified skin of the flank of rabbits under occlusive conditions (according to Fed. Reg, 38, No, 187, §1500.41, p. 27029). Following the 24-hour treatment time the treated area was washed with water. Slight to moderate erythema and moderate edema of the intact skin were observed for 72 hours. At 72 hours these animals exhibited scaling, which was still observed on day 8. Necrosis was observed in 1/6 animals (intact skin).
Overall, o-toluidine was evaluated as skin irritating.
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