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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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
Reference
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





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

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.

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
Reference
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





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

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.

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
Reference
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.

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.