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EC number: 201-924-9 | CAS number: 89-62-3
- 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
Endpoint summary
Administrative data
Description of key information
From the available results; the chemical 2-nitro-p-toluidine, is expected to exhibit acute toxic effects in the category 4 (based upon the LD50 and LC50 values mentioned in the CLP regulation) by the oral, inhalation and dermal route.
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- (Q)SAR
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Justification for type of information:
- QSAR prediction: migrated from IUCLID 5.6
- Qualifier:
- according to guideline
- Guideline:
- other:
- Principles of method if other than guideline:
- Prediction is done using QSAR Toolbox version 2.3.
- GLP compliance:
- no
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Control animals:
- not specified
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 590.944 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: other details not available
- Interpretation of results:
- Toxicity Category IV
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The acute oral median lethal dose (LD50) of 2-nitro-p-toluidine in rat (Rattus norvegicus) was found to be 590.9436 mg/kg of body weight. Acute toxicity of 2-nitro-p-toluidine to rat by the oral route indicates that the substance exhibits acute toxicity category IV by the oral route.
- Executive summary:
The acute oral median lethal dose (LD50) of 2-nitro-p-toluidine in rat (Rattus norvegicus) was found to be 590.9436 mg/kg of body weight. Acute toxicity of 2-nitro-p-toluidine to rat by the oral route indicates that the substance shall exhibit acute toxicity in category IV by the oral route.
Reference
The prediction was based on dataset comprised from the following descriptors: LD50
Estimation method: Taking average value from the 5 nearest neighbours
Domain logical expression:Result: In Domain
((("a" and "b" ) and "c" ) and ("d" and "e" ) )
Domain logical expression index: "a"
Similarity boundary:Target: c1(N)c(N(=O)=O)cc(C)cc1
Threshold=50%,
Dice(Atom pairs)
Domain logical expression index: "b"
Referential boundary: The target chemical should be classified as High (Class III) by Toxic hazard classification by Cramer (with extension)
Domain logical expression index: "c"
Similarity boundary:Target: c1(N)c(N(=O)=O)cc(C)cc1
Threshold=60%,
Dice(Atom pairs)
Domain logical expression index: "d"
Parametric boundary:The target chemical should have a value of log Kow which is >= 1.91
Domain logical expression index: "e"
Parametric boundary:The target chemical should have a value of log Kow which is <= 3.1
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 590.944 mg/kg bw
- Quality of whole database:
- Weight of evidence approach has been used using predictions from model considered reliable by OECD and authoritattive Swedish chemical agency database.
Acute toxicity: via inhalation route
Link to relevant study records
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- (Q)SAR
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Justification for type of information:
- QSAR prediction: migrated from IUCLID 5.6
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- GLP compliance:
- no
- Test type:
- other: Acute Rodent Inhalation Toxicity Test;standard acute method
- Species:
- rat
- Strain:
- other: Wistar;CnR-CD;Sprague-Dawley;Long-Evans;no data
- Sex:
- not specified
- Route of administration:
- inhalation
- Type of inhalation exposure:
- other: Inhalation: Vapor
- Vehicle:
- not specified
- Duration of exposure:
- 4 h
- Control animals:
- not specified
- Sex:
- not specified
- Dose descriptor:
- LC50
- Effect level:
- 19.317 other: mg/L
- Based on:
- test mat.
- Exp. duration:
- 4 h
- Interpretation of results:
- Toxicity Category IV
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The 4 hr acute inhalation median lethal concentration (LC50) of 2-nitro-p-toluidine in rat was estimated to be 19.31692 mg/L. Acute inhalation toxicity of 2-nitro-p-toluidine to rat by inhalative route indicates that the substance exhibits acute toxicity Category IV type by the inhalative route.
- Executive summary:
The 4 hr acute inhalation median lethal concentration (LC50) of 2-nitro-p-toluidine in rat was estimated to be 19.31692 mg/L. Acute inhalation toxicity of 2-nitro-p-toluidine to rat by inhalative route indicates that the substance exhibits acute toxicity Category IV type by the inhalative route.
Reference
The prediction was based on dataset comprised from the following descriptors: LC50
Estimation method: Taking average value from the 5 nearest neighbours
Domain logical expression:Result: In Domain
("a" and ("b" and "c" and "d" and "e" ) )
Domain logical expression index: "a"
Similarity boundary:Target: c1(N)c(N(=O)=O)cc(C)cc1
Threshold=50%,
Dice(Atom pairs)
Domain logical expression index: "b"
Parametric boundary:The target chemical should have a value of log Kow which is >= 2.15
Domain logical expression index: "c"
Parametric boundary:The target chemical should have a value of log Kow which is <= 3.2
Domain logical expression index: "d"
Parametric boundary:The target chemical should have a value of Molecular weight which is >= 137 Da
Domain logical expression index: "e"
Parametric boundary:The target chemical should have a value of Molecular weight which is <= 168 Da
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LC50
- Value:
- 19.316
- Quality of whole database:
- Model considered reliable by OECD
Acute toxicity: via dermal route
Link to relevant study records
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Qualifier:
- according to guideline
- Guideline:
- other:
- Principles of method if other than guideline:
- Kemi-Riskline database
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Species:
- guinea pig
- Strain:
- not specified
- Sex:
- not specified
- Type of coverage:
- not specified
- Vehicle:
- not specified
- Control animals:
- not specified
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- > 1 000 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: other details not available
- Interpretation of results:
- Toxicity Category IV
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Acute dermal toxicity value of 2-nitro-p-toluidine to guinea pig is found to be LD50: > 1000 mg/kg body weight. Thus, it is assumed that the chemical could potentially exhibit dermal toxicity in acute catergory 4 as per the CLP regulation guidelines.
- Executive summary:
Acute dermal toxicity value of 2-nitro-p-toluidine to guinea pig is found to be LD50: > 1000 mg/kg body weight. Thus, it is assumed that the chemical could potentially exhibit dermal toxicity in acute catergory 4 as per the CLP regulation guidelines.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 1 000 mg/kg bw
- Quality of whole database:
- Source of information is an authoritative database.
Additional information
The summary of the weight of evidence study of the acute toxicity by the oral route is presented below
S. No |
End point |
Value in mg/kg bw |
Species |
1 |
LC50 |
590.9436 |
Rattus norvegicus |
2 |
LC50 |
175.3525 |
Mouse (Mus musculus) |
3 |
LC50 |
1132.849 |
Mouse (Peromyscus maniculatus) |
4 |
LC50 |
1903 |
Rat (Rattus norvegicus) |
5 |
LC50 |
|
|
6 |
LC50 |
|
|
Justification for selection of acute toxicity – oral endpoint
Model considered reliable by OECD
Justification for selection of acute toxicity – inhalation endpoint
Model considered reliable by OECD and prediction suggests that the chemical 2-nitro-p-toluidine shall exhibit acute toxicity by the inhalation route in the category 4 sicen the LC50 value of 19.316 mg/L has been obtained
Justification for selection of acute toxicity – dermal endpoint
Acute dermal toxicity value of 2-nitro-p-toluidine to guinea pig is found to be LD50: > 1000 mg/kg body weight. Thus, it is assumed that the chemical could potentially exhibit dermal toxicity in acute catergory 4 as per the CLP regulation guidelines.
Justification for classification or non-classification
From the available results; the chemical 2-nitro-p-toluidine, is expected to exhibit acute toxic effects in the category 4 (based upon the LD50 and LC50 values mentioned in the CLP regulation) by the oral, inhalation and dermal route.
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.
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