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EC number: 200-805-9 | CAS number: 74-11-3
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in chemico
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11.05.2021 - 18.05.2021
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 021
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 442C (In Chemico Skin Sensitisation Assays addressing the Adverse Outcome Pathway key event on covalent binding to proteins)
- Version / remarks:
- Adopted: 26 June 2020
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- direct peptide reactivity assay (DPRA)
- Justification for non-LLNA method:
- approved alternative to animal testing
Test material
- Reference substance name:
- 4-chlorobenzoic acid
- EC Number:
- 200-805-9
- EC Name:
- 4-chlorobenzoic acid
- Cas Number:
- 74-11-3
- Molecular formula:
- C7H5ClO2
- IUPAC Name:
- 4-chlorobenzoic acid
- Test material form:
- solid: particulate/powder
- Details on test material:
- white to yellowish
Constituent 1
In chemico test system
- Details of test system:
- cysteine peptide, (Ac-RFAACAA-COOH)
- lysine peptide (Ac-RFAAKAACOOH)
- Details on the study design:
- The DPRA is a chemistry-based assay. Nucleophile-containing synthetic peptides (cysteine peptideAc-RFAACAA-COOH; lysine peptide- Ac-RFAAKAA-COOH) are used to screen for skin sensitisation potential by measuring peptide depletion following incubation with allergens and non-allergens.
Synthetic heptapeptides containing either cysteine or lysine are incubated with the test item at 25 °C for 24 hours. Depletion of the peptide in the reaction mixture is measured by high pressure liquid chromatography (HPLC) using UV detection. Average peptide depletion data for cysteine and lysine are then calculated. - Vehicle / solvent:
- mix DMSO:acetonitrile
- Positive control:
- cinnamic aldehyde
Results and discussion
- Positive control results:
- The mean percent peptide depletion value at 220 nm for the positive control Cinnamaldehyde is 71.0 % for the Cysteine peptide.
The mean percent peptide depletion value at 220 nm for the positive control Cinnamaldehyde is 58.6 % for the Lysine peptide.
In vitro / in chemico
Resultsopen allclose all
- Group:
- test chemical
- Run / experiment:
- run/experiment 1
- Parameter:
- cysteine depletion
- Value:
- 1.1 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Group:
- test chemical
- Run / experiment:
- run/experiment 2
- Parameter:
- cysteine depletion
- Value:
- 0.4 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Group:
- test chemical
- Run / experiment:
- run/experiment 3
- Parameter:
- cysteine depletion
- Value:
- 2.1 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Group:
- test chemical
- Run / experiment:
- mean
- Parameter:
- cysteine depletion
- Value:
- 1.2 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Group:
- test chemical
- Run / experiment:
- run/experiment 1
- Parameter:
- lysine depletion
- Value:
- 0.8 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Group:
- test chemical
- Run / experiment:
- run/experiment 2
- Parameter:
- lysine depletion
- Value:
- 0.6 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Group:
- test chemical
- Run / experiment:
- run/experiment 3
- Parameter:
- lysine depletion
- Value:
- 0.4 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Group:
- test chemical
- Run / experiment:
- mean
- Parameter:
- lysine depletion
- Value:
- 0.6 %
- At concentration:
- 100 mM
- Vehicle controls validity:
- valid
- Negative controls validity:
- valid
- Positive controls validity:
- valid
- Outcome of the prediction model:
- no or minimal reactivity [in chemico]
- Other effects / acceptance of results:
- All study acceptance criteria have been successfully met.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- 4-Chlorobenzoic acid was classified as negative in the DPRA (OECD Test 442C: In Chemico Skin Sensitisation). It was assigned to reactivity class: No or minimal reactivity.
- Executive summary:
The purpose of the test is to contribute to the evaluation of the skin sensitisation potential of 4-chlorobenzoic acid.
The test was performed according to OECD TG 442C, In Chemico Skin Sensitisation: Assays addressing the Adverse Outcome Pathway key event on covalent binding to proteins, Adopted: 26June 2020, Appendix I:The Direct Peptide Reactivity Assay (DPRA)
In the study, 4-chlorobenzoic acid was dissolved in dimethyl sulfoxide with acetonitrile, based on the results of the pre-experiments. The stock solution at concentration 100 mM was prepared based on a molecular weight of 156.56 g/mol.
The test item solutions were tested by incubating the samples with synthetic heptapeptides containing either cysteine or lysine at 25 °C for 24 ± 2 h. Depletion of the peptide in the reaction mixture was measured by HPLC with UV detection. Average peptide depletion data for cysteine and lysine were calculated. Cinnamaldehyde (100 mM) was used as a positive control and 1-butanol (100 mM) was used as a negative control. Each test chemical was prepared and analysed in triplicate for both peptides.
Samples were visually inspectedprior to the start of incubation andprior to HPLC analysis.
Immediately after addition of the Cysteine peptide to the solutions, there were any turbity or cloudiness, any colour changes in the vials. There were not any turbity or cloudiness, any colour changes in the vials after 24-hour incubation.
Immediately after addition of the Lysine peptide to the positive control, slight whitish turbidity was observed in the vial.The other vials were clear. The yellowish sediment on the bottom and on the wall of the vials with positive control was presented after 24-hour incubation. There was fine precipitate in the vials with test item.The other vials were clear with no color change, no turbidity and no precipitate in the vial. A phase separation was not observed for individual peptides.
All studyacceptance criteria have been successfully met.
The mean of Cysteine and Lysine percent depletion values is 0.9 %. Based on the obtained results, the prediction model the Cysteine 1:10/Lysine 1:50 was used for evaluation. The test item, 4-chlorobenzoic acid, has been found negative in the DPRA prediction; it was assigned to reactivity class “no or minimal reactivity”for both peptides.
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