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EC number: 201-746-1 | CAS number: 87-44-5
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 19 June 2000 to 27 June 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- The standard information requirements for REACH Annex VII substances for serious eye damage/eye irritation can be satisfied by an assessment of the available in vivo data, physicochemical properties (i.e. acid or alkali reserve) or in vitro eye irritation studies. Conducted prior to the validation and regulatory acceptance of alternative methods, a reliable (Klimisch 1) and GLP compliant in vivo Draize test was available for the test substance and considered sufficient to fulfil the information requirement.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 000
- Report date:
- 2000
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- 1987
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Version / remarks:
- 1997
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Caryophyllene
- EC Number:
- 201-746-1
- EC Name:
- Caryophyllene
- Cas Number:
- 87-44-5
- Molecular formula:
- C15H24
- IUPAC Name:
- (1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- other: Chbb:HM (SPF)
- Remarks:
- albino
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 2.7 to 2.9 kg b.w.
- Housing: Caged individually in PPO cages (floor area: 2576 sq.cm) with perforated floor
- Diet: Pelleted complete rabbit diet, ad libitum (Altromin 2123)
- Water: Domestic quality drinking water acidified with hydrochloric acid to pH 2.5, ad libitum
- Acclimation period: At least one week
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ± 3°C
- Humidity (%): 55 ± 15%
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12 hours light and 12 hours darkness
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied: 0.1 mL - Duration of treatment / exposure:
- Single exposure
- Observation period (in vivo):
- At 1, 24, 48 and 72 hours and 7 days after treatment
- Number of animals or in vitro replicates:
- 4
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing: Eyes were rinsed with 20 mL 0.9% sodium chloride solution
- Time after start of exposure: Eyes were rinsed 24 hours after exposure
SCORING SYSTEM:
When Fluorescein was used the cornea reactions were scored both before and alter the instillation of Fluorescein.
Cornea - Opacity degree of density (Area most dense taken for reading)
0: No ulceration or opacity.
1: Scattered or diffuse area of opacity (other than slight dulling of normal luster), details of iris clearly visible.
2: Easily discernible translucent areas, details of iris slightly obscured.
3: Nacreous areas, no details of iris visible, size of pupil barely discernible.
4: Complete corneal opacity, iris not discernible.
Area of cornea involved
1: One quarter (or less) but not zero.
2: More than 1 quarter, but less than half.
3: More than half, but less than 3 quarters.
4: More than 3 quarters, up to whole area.
Iris
0: Normal.
1: Markedly deepened folds, congestion, swelling, moderate circumcorneal injection (any of these or combination of any thereof), iris still reacts to light (sluggish reaction is positive).
2: No reaction to light, haemorrhage, gross destruction (any or all of these).
Conjunctiva redness (refers to palpebral and bulbar conjunctivae excluding cornea and Iris)
0: Vessels normal.
1: Some vessels definitely injected.
2: Diffuse, crimson red, individual vessels not easily discernible.
3: Diffuse beefy red.
Conjunctiva chemosis:
0: No swelling.
1: Any swelling above normal (includes nictitating membrane).
2: Obvious swelling with partial eversion of lids.
3: Swelling with lids about half closed.
4: Swelling with lids more than half closed.
Conjunctiva discharge:
0: No discharge.
1: Any amount different from normal (does not include small amounts observed in inner canthus of normal animals).
2: Discharge with moistening of the lids and hairs just adjacent to lids.
3: Discharge with moistening of the lids and hairs, and considerable area around the eye.
TOOL USED TO ASSESS SCORE: fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Remarks:
- (1813)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Remarks:
- (1815)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Remarks:
- (1816)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #4
- Remarks:
- (1817)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Remarks:
- (1813)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Remarks:
- (1815)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Remarks:
- (1816)
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 1
- Reversibility:
- fully reversible
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 1
- Reversibility:
- fully reversible
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Remarks:
- (1813)
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #2
- Remarks:
- (1815)
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #3
- Remarks:
- (1816)
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- fully reversible within: 72 hours
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #4
- Remarks:
- (1817)
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1.2
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Remarks:
- (1813)
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 2
- Reversibility:
- fully reversible within: 72 hours
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Remarks:
- (1815)
- Time point:
- 24/48/72 h
- Score:
- 0.67
- Max. score:
- 2
- Reversibility:
- fully reversible within: 72 hours
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Remarks:
- (1816)
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- chemosis score
- Basis:
- animal #4
- Remarks:
- (1817)
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 2
- Reversibility:
- fully reversible within: 72 hours
- Remarks on result:
- probability of weak irritation
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.8
- Max. score:
- 2
- Reversibility:
- fully reversible within: 7 d
- Remarks on result:
- probability of weak irritation
- Irritant / corrosive response data:
- One hour following application of the test article all four animals exhibited a diffuse, crimson red conjunctiva with individual vessels not easily discernible with partial eversion of lids. Animal 1 (#1813) and Animal 4 (#1817) also presented a discharge and an iris with markedly deepened folds, congestion, swelling, moderate circumcorneal injection, respectively. The mean values for corneal opacity, iris lesions, redness of conjunctivae and oedema of conjunctivae (chemosis) were 0.0, 0.0, 1.2 and 0.8, respectively. All weak signs of irritation were reversible and 7 days after application of the test article all four animals were free of any signs of eye irritation.
Any other information on results incl. tables
Table 1. Scores for ocular lesions
Ocular lesion | Animal number | 1 h | 24 h (after Fluorescein) | 48 h | 72 h |
7 days |
Cornea opacity, degree |
1 |
0 |
0 (0) |
0 |
0 |
0 |
0 | 2 | 0 | 0 (0) | 0 | 0 | 0 |
3 | 0 | 0 (0) | 0 | 0 | 0 | |
4 | 0 | 0 (0) | 0 | 0 | 0 | |
Cornea opacity, area | 1 | 0 | 0 (0) | 0 | 0 | 0 |
2 | 0 | 0 (0) | 0 | 0 | 0 | |
3 | 0 | 0 (0) | 0 | 0 | 0 | |
4 | 0 | 0 (0) | 0 | 0 | 0 | |
Iris | 1 | 0 | 0 | 0 | 0 | 0 |
2 | 0 | 0 | 0 | 0 | 0 | |
3 | 0 | 0 | 0 | 0 | 0 | |
4 | 1 | 0 | 0 | 0 | 0 | |
Conjunctiva redness | 1 | 2 | 2 | 1 | 1 | 0 |
2 | 2 | 2 | 1 | 1 | 0 | |
3 | 2 | 2 | 1 | 0 | 0 | |
4 | 2 | 2 | 1 | 1 | 0 | |
Conjunctiva chemosis | 1 | 2 | 1 | 1 | 0 | 0 |
2 | 2 | 1 | 1 | 0 | 0 | |
3 | 2 | 1 | 1 | 1 | 0 | |
4 | 2 | 2 | 1 | 0 | 0 | |
Conjunctiva discharge | 1 | 1 | 0 | 0 | 0 | 0 |
2 | 0 | 0 | 0 | 0 | 0 | |
3 | 0 | 0 | 0 | 0 | 0 | |
4 | 0 | 0 | 0 | 0 | 0 |
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The mean values for corneal opacity, iris lesions, redness of conjunctivae and oedema of conjunctivae (chemosis) were 0.0, 0.0, 1.2 and 0.8, respectively. All weak signs of irritation were reversible and 7 days after application of the test article all four animals were free of any signs of eye irritation. The test item should not be classified as irritating to the eye, according to the directive of the EEC commission 93/21/EEC and GHS/EU CLP criteria.
- Executive summary:
The study was initiated with one rabbit, since no marked eye irritation was observed, another three rabbits were included. An aliquot of 0.1 mL test item was instilled into the conjunctival sac of one eye of each rabbit, while the other eye remained untreated and was used as the negative control. Assessments of damage/irritation (cornea opacity, iris lesion, conjunctival redness and conjunctival oedema) were made 1, 24, 48 and 72 hours, in addition to 7 days, following treatment.
Weak conjunctival inflammation, accompanied by slight swelling was observed in all four rabbits for up to 72 hours after instillation. The mean values for corneal opacity, iris lesions, redness of conjunctivae and oedema of conjunctivae (chemosis) were 0.0, 0.0, 1.2 and 0.8, respectively. All weak signs of irritation were reversible and 7 days after application of the test article all four animals were free of any signs of eye irritation. The test material should not be classified as irritating to the eye, according to the directive of the EEC commission 93/21/EEC (4 May 1993) and GHS/EU CLP criteria. Conducted according to OECD TG 405 (EU Method B.5) and GLP, the study was considered to be reliable (Klimisch 1).
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