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Diss Factsheets
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EC number: 945-149-0 | CAS number: -
- 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 irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- No data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- no details on test animals and environmental conditions; no details on patch material; observations not followed until the reversibility of the effects (only 7 days)
- Justification for type of information:
- The in vivo test was performed before the REACH regulation came into force, requesting in vitro studies. This information is used for read across to Terpene hydrocarbon alcohols
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 995
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- . There is no certificate of analysis of the test substance; no details on test animals and environmental conditions; no details on patch material; and observations are not followed until the reversibility of the effects (only 7 days).
- GLP compliance:
- yes
Test material
- Reference substance name:
- p-menth-1-en-8-ol
- EC Number:
- 202-680-6
- EC Name:
- p-menth-1-en-8-ol
- Cas Number:
- 98-55-5
- Molecular formula:
- C10H18O
- IUPAC Name:
- 2-(4-methylcyclohex-3-en-1-yl) propan-2-ol
- Test material form:
- other: liquid
- Details on test material:
- - Name of test material (as cited in study report): Terpineol alpha
- Source: Givaudan-Roure
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- other: albino
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume with unit): 0.5 mL - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 7 days
- Number of animals:
- Test 1: 3
Test 2&3: 4 - Details on study design:
- SCORING SYSTEM: Draize scoring system
- tested in a multi-patch study
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 1
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 2.44
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 1
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 2.17
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 2
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 2.58
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 2
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 1.92
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 3
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- all animals
- Time point:
- 24/48/72 h
- Score:
- 2.08
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 7 days
- Remarks on result:
- other: Test 3
- Irritant / corrosive response data:
- Test 1: Two animals showed marked desquamation at the 7 day time interval. The other animal showed thickening and marked desquamation of the skin surface at the 7 day time interval.
Test 2: One animal showed slight desquamation at the 7 day time interval. The three other animals showed marked desquamation at the 7 day time interval.
Test 3: Two animals showed slight desquamation at the 7 day time interval. One animal showed slight desquamation at the 2, 3, and 7 day time interval. One animal showed marked desquamation at the 7 day time interval
Any other information on results incl. tables
Test 1
|
1 hr |
1 day |
2 days |
3 days |
7 days |
Mean (24, 48, 72 hrs) |
Animal No. 1 |
||||||
Erythema |
0 |
1 |
2 |
2 |
1 |
1.67 |
Oedema |
1 |
2 |
2 |
2 |
1 |
2 |
Animal No. 2 |
|
|||||
Erythema |
2 |
2 |
2 |
2 |
2 |
2 |
Oedema |
2 |
3 |
2 |
2 |
1 |
2.33 |
Animal No. 3 |
|
|||||
Erythema |
2 |
2 |
2 |
3 |
3 |
2.33 |
Oedema |
2 |
3 |
3 |
3 |
3 |
3 |
Test 2
|
1 hr |
1 day |
2 days |
3 days |
7 days |
Mean (24, 48, 72 hrs) |
Animal No. 1 |
||||||
Erythema |
2 |
2 |
2 |
2 |
2 |
2 |
Oedema |
2 |
3 |
3 |
3 |
1 |
3 |
Animal No. 2 |
|
|||||
Erythema |
2 |
2 |
3 |
3 |
2 |
2.67 |
Oedema |
3 |
3 |
3 |
3 |
3 |
3 |
Animal No. 3 |
|
|||||
Erythema |
2 |
2 |
2 |
2 |
2 |
2 |
Oedema |
2 |
3 |
2 |
3 |
3 |
2.67 |
Animal No. 4 |
|
|||||
Erythema |
1 |
2 |
2 |
2 |
1 |
2 |
Oedema |
2 |
2 |
2 |
1 |
0 |
1.67 |
Test 3
|
1 hr |
1 day |
2 days |
3 days |
7 days |
Mean (24, 48, 72 hrs) |
Animal No. 1 |
||||||
Erythema |
2 |
2 |
2 |
2 |
1 |
2 |
Oedema |
2 |
3 |
3 |
2 |
0 |
2.67 |
Animal No. 2 |
|
|||||
Erythema |
2 |
2 |
2 |
2 |
2 |
2 |
Oedema |
2 |
2 |
2 |
2 |
2 |
2 |
Animal No. 3 |
|
|||||
Erythema |
1 |
2 |
2 |
1 |
0 |
1.67 |
Oedema |
0 |
1 |
1 |
0 |
0 |
0.67 |
Animal No. 4 |
|
|||||
Erythema |
2 |
2 |
2 |
2 |
1 |
2 |
Oedema |
1 |
3 |
3 |
3 |
1 |
3 |
Applicant's summary and conclusion
- Interpretation of results:
- other: Skin irritant Cat. 2
- Remarks:
- according to EU CLP (EC No. 1272/2008 and its amendments).
- Conclusions:
- Mean individual scores at 24, 48 and 72 h after exposure for the 3 animals of the first test were 1.67, 2 and 2.33 for erythema score and 2, 2.33 and 3 for edema score. For the second test the mean individual scores were 2, 2.67, 2 and 2 for erythema score and 3, 3, 2.67 and 1.67 for edema score. For the third test the mean individual scores were 2, 2, 1.67 and 2 for erythema score and 2.67, 2, 0.67 and 3 for edema score. Under the test conditions the substance is considered to be irritating to the skin because the average oedema score exceeded 2.5 (CLP) and the effects were not fully reversible within the observation period of 7 days
- Executive summary:
In three primary dermal irritation studies performed according to OECD guideline 404 and in compliance with GLP, three or four albino rabbits were dermally exposed to 0.5 mL of undiluted alpha-Terpineol under a semi-occlusive patch for 4 hours to intact skin of the flank. Animals were then observed for 7 days. Irritation was scored by the method of Draize at 1, 24, 48 and 72 hours and 7 days after exposure. Mean individual scores at 24, 48 and 72 h after exposure for the 3 animals of the first test were 1.67, 2 and 2.33 for erythema score and 2, 2.33 and 3 for edema score. For the second test the mean individual scores were 2, 2.67, 2 and 2 for erythema score and 3, 3, 2.67 and 1.67 for edema score. For the third test the mean individual scores were 2, 2, 1.67 and 2 for erythema score and 2.67, 2, 0.67 and 3 for edema score. Under the test conditions the substance is considered to be irritating to the skin because the average oedema score exceeded 2.5 and the effects were not fully reversible within the observation period of 7 days.
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