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EC number: 413-370-7 | CAS number: 17351-75-6 RAPICURE CHVE
- 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
1,4 -bis[(vinyloxy)methyl]cyclohexane is irritating to skin but not irritating to eyes.
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:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Minor deviations to OECD Guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- abraded and non abraded skin
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: CAMM Resarch (Wayne, NJ, USA)
- Weight at study initiation: ca. 2 kg
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 4 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18,3 -23,9 °C (65 - 75 °F)
- Photoperiod (hrs dark / hrs light): 12 - Type of coverage:
- semiocclusive
- Preparation of test site:
- other: abraded and non-abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0,5 ml - Duration of treatment / exposure:
- 24 h
- Observation period:
- 72 h
- Number of animals:
- 6
- Details on study design:
- TEST SITE
- Area of exposure: 2,5 cm² (flank)
- Type of wrap if used: J&J gauze sponge, Webril pad, J&J dermicel hypo-allergenic cloth tape
REMOVAL OF TEST SUBSTANCE
- Washing (if done): water
- Time after start of exposure: 24 h
SCORING SYSTEM:Draize - Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 0.8
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 h
- Remarks on result:
- other: (non-Abraded)
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 0.7
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 h
- Remarks on result:
- other: (non-abraded)
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72
- Score:
- 2.3
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 h
- Remarks on result:
- other: (non-abraded)
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72
- Score:
- 1.8
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 72 h
- Remarks on result:
- other: (non abraded)
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 24 -72 h
- Score:
- 3.2
- Reversibility:
- not fully reversible within: 72 h
- Irritant / corrosive response data:
- Skin was discribed as bleached in 2/6 animal 24 h post application.
Skin was discribed as dry in 3/6 animal 72 h post application.
1/6 animals had a fisur 72 h post aplication.
Except edema after 72 h (score 2.7) results on abraded skin were in the same range as those on non-abraded skin. - Interpretation of results:
- irritating
- Remarks:
- Migrated information
- Executive summary:
The study is reliable with restrictions due to some deviations to the OECD Guideline. The test substance was applied on abraded and non-abraded skin of 6 rabbits. Edema (max.3 of 4 ) and Erythem (max. 4 of 4) was observed. Primary dermal irritation index was 3.2.
The study was terminated 72 h post application and effects were not fully reversible within this time.
Conclusion
1,4 -bis[(vinyloxy)methyl]cyclohexane is irritating to the skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Only study summary availiable
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- no
- Principles of method if other than guideline:
- J.H. Draize, "Dermal Toxicity", Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics, (The Association of Food and Drug Officials of the United States, (1975), pp. 52 - 54.
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: CAMM Research (Wayne, NJ, USA)
- Age at study initiation: approx. 3 month
- Weight at study initiation: approx. 2 kg
- Housing: single
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 3 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18.3 - 23,9 °C (65 - 75 ° F)
- Photoperiod (hrs dark / hrs light): 12 h - Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 ml - Duration of treatment / exposure:
- The eyes of six (6) animals remained unwashed for 24 hours; the eyes of the remaining three (3) animals were washed out 30 seconds after instillation of the test article.
- Observation period (in vivo):
- Observations of corneal opacity, iritis, conjunctivitis, and other effects were recorded 24, 48, and 72 hours after treatment, and at day 4.
- Number of animals or in vitro replicates:
- 9
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): yes
- Time after start of exposure: 30 Minutes after start of exposure 3 rabbits and 24 h after start of exposure 6 rabbits.
SCORING SYSTEM:
Draize - Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24 - 72
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- other: only unwashed eyes data
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24-72
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- other: only unwashed eyes data
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24-72
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- other: only unwashed eyes data
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 24 - 72
- Score:
- 0.2
- Max. score:
- 1
- Reversibility:
- fully reversible
- Remarks on result:
- other: only unwashed eyes data; reverible within 4 days
- Irritant / corrosive response data:
- Only minimal irritation effects were observed
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information
- Executive summary:
The study is a guideline study according to US cosmetics regulation. However, the study is reliable with restriction because there is only a summary availiable which provides poor information concerning the test substance identity.
Nine New Zealand white rabbits, free from visible ocular defects, each received a cingle intraocular application of 0.1 milliliter of the test article. The contralateral eye, remaining untreated, served as a control. The eyes of six animals remained unwashed for 24 hours; the eyes of the remaining three animals were washed out 30 seconds after instillation of the test article. Observations of corneal opacity, iritis, conjunctivitis, and other effects were recorded 24, 48, and 72 hours after treatment, and at day 4.
The instillation of 1,4 dimethylol-divinylether cyclohexane resulted in a slight erythema (mean 0.2), but no other effect was observed for the unwashed eye. Therefore 1,4 dimethylol-divinylether cyclohexane was considered not irritating to the eyes (score 0.3 of max 110) .
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
The irritation potential of 1,4 -bis[(vinyloxy)methyl]cyclohexane was examined in studies which were comparable to guideline studies.
Skin
1,4 -bis[(vinyloxy)methyl]cyclohexane was applied on abraded and non-abraded skin of 6 rabbits at semiocclusive conditions. Edema (max.3) and Erythem (max. 4) was observed. The study was terminated 72 h post application and effects were not fully reversible within this time. Primary dermal irritation index was 3.2 which is moderately irritating to the skin.
Eye
9 New Zealand white rabbits, free from visible ocular defects, received a single intraocular application of 0.1 milliliter of
1,4 -bis[(vinyloxy)methyl]cyclohexane. The contralateral eye, remaining untreated, served as a control. The eyes of six animals remained unwashed for 24 hours; the eyes of the remaining three animals were washed out 30 seconds after instillation of the test article. Observations of corneal opacity, iritis, conjunctivitis, and other effects were recorded 24, 48, and 72 hours after treatment, and at day 4. The instillation of 1,4 -bis[(vinyloxy)methyl]cyclohexane resulted in a slight erythema (mean 0.2), but no other effect was observed for the unwashed eye. Therefore, 1,4 -bis[(vinyloxy)methyl]cyclohexane is not considered irritating to the eyes (score 0.3 of max 110) .
Justification for selection of skin irritation / corrosion endpoint:
Only one study available
Justification for selection of eye irritation endpoint:
Only one study available
Effects on skin irritation/corrosion: irritating
Justification for classification or non-classification
Classification for skin irritation (cat. 2) is warranted according to the criteria of EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.
Classification for eye irritation is not warranted according to the criteria of EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.
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