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EC number: 203-139-7 | CAS number: 103-73-1
- 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
Skin Irritation
Administration of the test chemical to the rabbit resulted in a slight skin irritation effect which is not adequate for classification as a skin irritant. Therefore, it can be concluded that the test chemical was not irritating to skin.
Eye Irritation
By applying the weight of evidence approach, the test chemical can be estimated to be irritating to eyes. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Category 2".
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- data is from handbooks and authoritative databases
- Qualifier:
- according to guideline
- Guideline:
- other: as mentioned below
- Principles of method if other than guideline:
- To assess the dermal irritation potential of the test chemical
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): Phenetole
- Molecular Formula: C8H10O
- Molecular Weight: 122.17 g/mol
- Substance type: Organic
- Physical state: Liquid - Species:
- rabbit
- Strain:
- not specified
- Details on test animals or test system and environmental conditions:
- Not available
- Type of coverage:
- not specified
- Preparation of test site:
- not specified
- Vehicle:
- not specified
- Controls:
- not specified
- Amount / concentration applied:
- Not available
- Duration of treatment / exposure:
- Not available
- Observation period:
- Not available
- Number of animals:
- Not available
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: no data available
- Reversibility:
- not specified
- Remarks on result:
- positive indication of irritation
- Irritant / corrosive response data:
- Signs of slight irritation were observed
- Interpretation of results:
- other: not irritating
- Conclusions:
Administration of the test chemical to the rabbit resulted in a slight skin irritation effect which is not adequate for classification as a skin irritant. Therefore, it can be concluded that the test chemical was not irritating to skin.- Executive summary:
Administration of the test chemical to the rabbit resulted in a slight skin irritation effect which is not adequate for classification as a skin irritant. Therefore, it can be concluded that the test chemical was not irritating to skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Remarks:
- weight of evidence approach based on various test chemicals
- Justification for type of information:
- Weight of evidence approach based on various test chemicals
- Reason / purpose for cross-reference:
- read-across: supporting information
- Reason / purpose for cross-reference:
- read-across: supporting information
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- other: Weight of evidence approach based on various chemicals
- Principles of method if other than guideline:
- Weight of evidence approach based on various chemicals
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): Phenetole
- Molecular Formula: C8H10O
- Molecular Weight: 122.17 g/mol
- Substance type: Organic
- Physical state: Liquid - Species:
- rabbit
- Strain:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not specified
- Amount / concentration applied:
- 1. 100 mg
2. 0.1ml
3. 100 mg - Duration of treatment / exposure:
- single
- Observation period (in vivo):
- 1. 24h till 21 days
2. 24 hours
3. 24 hours - Number of animals or in vitro replicates:
- 1. 3
2. 6
3. no data available - Details on study design:
- The study is based on weight of evidence approach using various chemicals
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- 24 h
- Reversibility:
- not specified
- Remarks on result:
- positive indication of irritation
- Irritant / corrosive response data:
- Signs of irritation were observed
- Interpretation of results:
- Category 2 (irritating to eyes) based on GHS criteria
- Conclusions:
- The eye irritation potential of the test chemical was assessed based on the available results from the various test chemicals. By applying the weight of evidence approach, the test chemical can be estimated to be irritating to eyes. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Category 2".
- Executive summary:
The eye irritation potential of the test chemical was assessed based on the available results from the various test chemicals.
An ocular irritation study was conducted to determine adverse effects caused by the chemical in rabbits
100mg of the test chemical was instilled into the eyes of 3 rabbits and observed for effects from 24 hours till 21 days.
The test chemical caused corneal damage which persisted for more than 24 hours, but healed within 21 days.
Hence, the test chemical can be considered to be irritating to eyes.
This is supported by the results of an OECD 405 study performed to assess irritation potential of the other test chemical. 0.1ml undiluted test chemical was instilled into the eyes of 6 rabbits and eyes remained unwashed till 24 hours. The reactions were observed and scored according to the method of Draize.
The maximum stimulus index after 24 hours was 30/110 and the average stimulus index was 29.5/110.
Hence the test chemical was considered to be slightly irritating to the eyes and eye mucosa.
The above results are further supported by another ocular irritation performed in rabbits to assess the irritation potential of the test chemical. 100 mg of the undiluted test chemical was instilled into the eyes of the rabbits and observed for signs of irritation till 24 hours.
Moderate signs of irritation were observed. Hence, the test chemical was considered to be irritating to eyes.
By applying the weight of evidence approach, the test chemical can be estimated to be irritating to eyes. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Category 2".
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin Irritation
The skin irritation potential of the test chemical was assessed based on the available results from the various test chemicals.
Administration of the test chemical to the rabbit resulted in a slight skin irritation effect which is not adequate for classification as a skin irritant. Therefore, it can be concluded that the test chemical was not irritating to skin.
Skin irritation effects were also estimated by four different models i.e, Battery, Leadscope, SciQSAR and CASE Ultra used within Danish QSAR database for the test chemical. Based on estimation, no severe skin irritation effects were known when the test chemical was exposed to rabbit skin. Hence, the test chemical can be considered not irritating to skin.
The estimated and experimental results are in agreement with each other, indicating that the test chemical can be not irritating to skin.
The above studies are supported by the results of Repeated insult patch test performed to assess the dermal irritation of the test chemical
The test chemical (10% v/v in mineral oil) was tested for irritation and sensitization using a panel of 51 subjects (male and female), aged 16- >60. 0.3 ml Test material was applied to a patch that was then applied to the skin of the upper arm of the panelist. The patches were removed 24 hr after application.
Two panelists had reaction scores of 1 (reaction visible but mild), one after induction 3 and another after induction 5 (reactions were noted before application of patches 4 and 6). In both cases, the reaction cleared by the application of the next patch. Hence the test chemical was considered to be not irritating to humans.
These results are supported by a Draize test performed to assess the dermal irritation potential of the test chemical
Test material (0.5 ml) was held in continous 24-hour contact with the skin of rabbits under an impervious patch. Skin was abraded at one site. Irritation was observed 24 and 72 hours after removal of the patch. The primary irritation score was assessed to be 0.04.The test substance was found to be not irritating to rabbit skin.
By applying the weight of evidence approach, the test chemical can be considered to be not irritating to skin. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Not Classified".
Eye Irritation:
The eye irritation potential of the test chemical was assessed based on the available results from the various test chemicals.
An ocular irritation study was conducted to determine adverse effects caused by the chemical in rabbits
100mg of the test chemical was instilled into the eyes of 3 rabbits and observed for effects from 24 hours till 21 days.
The test chemical caused corneal damage which persisted for more than 24 hours, but healed within 21 days.
Hence, the test chemical can be considered to be irritating to eyes.
This is supported by the results of an OECD 405 study performed to assess irritation potential of the other test chemical. 0.1ml undiluted test chemical was instilled into the eyes of 6 rabbits and eyes remained unwashed till 24 hours. The reactions were observed and scored according to the method of Draize.
The maximum stimulus index after 24 hours was 30/110 and the average stimulus index was 29.5/110.
Hence the test chemical was considered to be slightly irritating to the eyes and eye mucosa.
The above results are further supported by another ocular irritation performed in rabbits to assess the irritation potential of the test chemical. 100 mg of the undiluted test chemical was instilled into the eyes of the rabbits and observed for signs of irritation till 24 hours.
Moderate signs of irritation were observed. Hence, the test chemical was considered to be irritating to eyes.
By applying the weight of evidence approach, the test chemical can be estimated to be irritating to eyes. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Category 2".
Justification for classification or non-classification
Available results for the test chemicals indicate a possibility that the test chemical can be considered to be not irritating to skin.
Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Not Classified".
By applying the weight of evidence approach, the test chemical can be estimated to be irritating to eyes. Comparing the annotations with criteria of CLP regulation, the test chemical can be classified under the category "Category 2".
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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