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EC number: 218-691-4 | CAS number: 2216-52-6
- 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:
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.
Eye Irritation:
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be not irritating to eyes.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomentholcan be classified under the category “Not Classified”.
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin 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:
- other: Weight of evidence approach based on structurally similar substances
- Justification for type of information:
- Weight of evidence approach based on structurally similar substances
- 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 structurally similar substances
- Principles of method if other than guideline:
- Weight of evidence approach based on structurally similar substances
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Name of the test chemical: (1S,2S,5R)-5-methyl-2-propan-2-ylcyclohexan-1-olCommon Name: (+)-NeomentholMolecular Formula: C10H20OMolecular Weight: 156.269 g/molSubstance Type: OrganicPhysical State: Solid
- Species:
- rabbit
- Strain:
- not specified
- Type of coverage:
- other: 1. open, 2. occlusive
- Preparation of test site:
- other: 1. hairless, 2. intact and abraded skin
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not specified
- Amount / concentration applied:
- 1. 0.05 ml2. 5 ml/kg
- Duration of treatment / exposure:
- 1.The dosing was repeated between 5 and 10 times2. 24 hours
- Observation period:
- 1. 2 weeks2. 24 hours
- Number of animals:
- 1. 52. 4
- Details on study design:
- The study is based on the weight of evidence approach based on structurally similar chemicals
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Reversibility:
- not specified
- Remarks on result:
- positive indication of irritation
- Irritant / corrosive response data:
- Signs of irritation observed
- Interpretation of results:
- Category 2 (irritant) based on GHS criteria
- Conclusions:
- Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.
- Executive summary:
Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the dermal irritation potential of (+)-Neomenthol
The dermal irritation potential of the structurally similar chemical was assessed in rabbits. Hairless sites on the skin of 5 White rabbits were intradermally injected with 0.05ml of the test chemical. The dosing was repeated between 5 and 10 times. Gross examinations were made at 24 and 48 hours, at 1 and 2 weeks and in some cases 1 month following dosing. Microscopic examination of the skin was performed after the gross examination.
Moderate reactions characterized by polymorphonucelar leukocytes, and plasma cells(without necrosis) were noted in 3 rabbits. Severe reactions as well as necrosis were noted in the other 2 rabbits.
Hence, the test chemical can be considered to be a skin irritant.
This is supported by the results of another dermal irritation study performed in rabbits to assess the irritation potential of structurally similar chemical. 5 ml/kg undiluted test chemical was applied to the intact and abraded skin of 4 rabbits under occlusive conditions for 24 hours. The readings for dermal reactions were taken after patch removal. Mild erythema was observed at 24 hours, but no edema. Hence, the test chemical can be considered to be irritating to rabbit skin.
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin Irritation:
Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the dermal irritation potential of (+)-Neomenthol
The dermal irritation potential of the structurally similar chemical was assessed in rabbits.
Hairless sites on the skin of 5 White rabbits were intradermally injected with 0.05ml of the test chemical. The dosing was repeated between 5 and 10 times. Gross examinations were made at 24 and 48 hours, at 1 and 2 weeks and in some cases 1 month following dosing. Microscopic examination of the skin was performed after the gross examination.
Moderate reactions characterized by polymorphonucelar leukocytes, and plasma cells(without necrosis) were noted in 3 rabbits. Severe reactions as well as necrosis were noted in the other 2 rabbits.
Hence, the test chemical can be considered to be a skin irritant.
This is supported by the results of another dermal irritation study performed in rabbits to assess the irritation potential of structurally similar chemical. 5 ml/kg undiluted test chemical was applied to the intact and abraded skin of 4 rabbits under occlusive conditions for 24 hours. The readings for dermal reactions were taken after patch removal. Mild erythema was observed at 24 hours, but no edema. Hence, the test chemical can be considered to be irritating to rabbit skin.
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be irritating to skin.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomenthol can be classified under the category “Category 2”.
Eye Irritation:
Based on the available studies for the structurally similar read across chemicals, weight of evidence approach was applied to assess the ocular irritation potential of (+)-Neomenthol
An eye irritation study was conducted on rabbits to assess the degree of eye irritancy caused by the structurally similar according to Draize method.
The test substance was initially applied in 10, 20 and 30 % solution. The eyes of 4 animals were rinsed 1 minute after application with physiological saline, substance remained in the eyes of 4 animals. In a second step animals were treated with concentration of 40, 50 and 60 %.
No signs of eye irritation were observed. Hence, the chemical was considered to be not irritating to the eyes of rabbits.
This is supported by the results of another ocular irritation study performed on rabbits to determine the degree of irritation caused by the structurally similar chemical.
Undiluted 0.1 ml of the test chemical was instilled in the right eye of 6 New Zealand White rabbits. The untreated left eye served as control. Reactions were scored as per the Draize method against the control, on days 1–8.
The mean irritation scores of the test group were 6.0 (24-h), 2.0 (48-h), 0.3 (96-h), and 0.0 respectively. The effects were fully reversible within 8 days.
Hence, the test chemical can be considered to be not irritating to eyes.
Based on the available data for the structurally similar read across substances and applying the weight of evidence approach, it can be concluded that the target chemical will also tend to behave in a similar that of the read across substances. Therefore, (+)-Neomenthol was estimated to be not irritating to eyes.Comparing the above annotations with the criteria of CLP regulation,(+)-Neomentholcan be classified under the category “Not Classified”.
Justification for classification or non-classification
The results of the experimental studies from the structurally similar read across substances indicate a possibility that (+)-Neomenthol can be irritating to skin but not irritating to eyes.
Hence by applying the weight of evidence approach, (+)-Neomenthol can be considered to be irritating to skin and not irritating to eyes. It can be classified under the category “Not Classified” for eye irritation and “Category 2” for skin irritation as per CLP regulation.
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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