L-Glutamic acid, N-coco acyl derivs., compds. with triethanolamine (1:1)

Endpoint summary

Description of key information

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Link to relevant study records

Reference

Reference 1

Endpoint:

repeated dose toxicity: oral, other

Remarks:

Both subchronic and subacute data were used in the prediction. As a worst case, the prediction is submitted as subacute toxicity data.

Type of information:

(Q)SAR

Adequacy of study:

key study

Study period:

2018

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: The following prediction was performed using the OECD QSAR Toolbox using an appropriate category based on the current endpoint. The prediction was further refined using subcategories.

Justification for type of information:

The test material is a mixture of many substances. Comparison of all substances has shown that they are expected to have the same repeat dose toxicity. For the purpose of addressing the repeat dose endpoint the most concentrated component of the test material was assessed individually.

Reason / purpose for cross-reference:

other: read-across target

Qualifier:

according to guideline

Guideline:

other: REACH Guidance on QSARs R.6, May/July 2008

Principles of method if other than guideline:

The repeat dose oral toxicity of the test material was evaluated using a read-across approach. Suitable analogues were found in the OECD QSAR Toolbox using the Organic Functional Groups category, and the results were refined using relevant subcategories.

GLP compliance:

no

Remarks:

As no laboratory work took place, compliance with GLP is not required.

Limit test:

no

Specific details on test material used for the study:

SMILES: OCC[N+H](CCO)CCO.CCCCCCCC(=O)NC(CCC(O)=O)C([O-])=O

Species:

rat

Strain:

not specified

Sex:

not specified

Route of administration:

oral: unspecified

Dose descriptor:

NOEL

Effect level:

1 080 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

not specified

Basis for effect level:

other: Based on the modelled conditions

Remarks on result:

not measured/tested

Remarks:

The prediction was based on the average value from the 4 nearest neighbours compared by prediction descriptors.

Critical effects observed:

not specified

The prediction was based on dataset comprised from the following descriptors: NOEL

Estimation method: Takes average value from the 4 nearest neighbours

Domain logical expression: Result: In Domain

Substances used for the prediction should be:

Alcohol<OR>Ammonium salt<OR>Carboxylic acid<OR>Organic amide and thioamide (Organic functional groups)

Not categorized ( Repeated dose (HESS))

Alcohol; Ammonium salt; Carboxylic acid; Organic amide and thioamide (Organic functional groups)

Conclusions:

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

Executive summary:

The repeat dose oral toxicity of the test material was evaluated using a read-across approach. Suitable analogues were found in the OECD QSAR Toolbox using the Organic Functional Groups profiler, and the results were refined using relevant subcategory (repeat dose (HESS)).

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

The target chemical falls within the applicability domain of the prediction.

Reference 2

Endpoint:

repeated dose toxicity: oral, other

Remarks:

Both subchronic and subacute data were used in the prediction. As a worst case, the prediction is submitted as subacute toxicity data.

Type of information:

read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Justification for type of information:

For the justification for read-across, please refer to the read-across assessment framework report that is attached to Section 13.

Reason / purpose for cross-reference:

read-across source

Species:

rat

Strain:

not specified

Sex:

not specified

Route of administration:

oral: unspecified

Dose descriptor:

NOEL

Effect level:

1 080 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

not specified

Basis for effect level:

other: Based on the modelled conditions

Remarks on result:

not measured/tested

Remarks:

The prediction was based on the average value from the 4 nearest neighbours compared by prediction descriptors.

Critical effects observed:

not specified

Conclusions:

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

Executive summary:

The repeat dose oral toxicity of the test material was evaluated using a read-across approach. Suitable analogues were found in the OECD QSAR Toolbox using the Organic Functional Groups profiler, and the results were refined using relevant subcategory (repeat dose (HESS)).

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

The target chemical falls within the applicability domain of the prediction.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion

Endpoint conclusion:

no study available

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion

Endpoint conclusion:

no study available

Repeated dose toxicity: dermal - systemic effects

Endpoint conclusion

Endpoint conclusion:

no study available

Repeated dose toxicity: dermal - local effects

Endpoint conclusion

Endpoint conclusion:

no study available

Additional information

The repeat dose oral toxicity of the test material was evaluated using a read-across approach. Suitable analogues were found in the OECD QSAR Toolbox using the Organic Functional Groups profiler, and the results were refined using relevant subcategory (repeat dose (HESS)).

Based on the modelled conditions, the subacute NOEL of the test material in the rat was determined to be ca. 1080 mg/kg bw/day.

Justification for classification or non-classification

In accordance with the criteria for classification as defined in Annex I, Regulation (EC) No. 1272/2008 (CLP), the substance does not require classification with respect to Specific Target Organ Toxicity repeated dose (STOT RE) via the oral route.