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EC number: 307-301-9 | CAS number: 97593-01-6
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2002-03-13 to 2002-03-16
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable with restrictions because it was conducted according to GLP guidance.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in Section 13.
Cross-reference
- Reason / purpose for cross-reference:
- read-across: supporting information
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- GLP compliance:
- yes
Test material
- Reference substance name:
- Tetradec-1-ene
- EC Number:
- 214-306-9
- EC Name:
- Tetradec-1-ene
- Cas Number:
- 1120-36-1
- Molecular formula:
- C14H28
- IUPAC Name:
- tetradec-1-ene
- Details on test material:
- - Name of test material (as cited in study report): Amodrill 1410
- Substance type: C14 alpha olefin
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Davidson's Mill Farm, South Brunswick, NJ
- Age at study initiation: Young adult
- Housing: Housed singly in suspended steel caging with mesh floors
- Diet (e.g. ad libitum): Pelleted Purina rabbit chow, ad libitum
- Water (e.g. ad libitum): filtered tap water, ad libitum
- Acclimation period: 14 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19-21
- Photoperiod (hrs dark / hrs light): 12 hrs dark/ 12 hrs light
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not specified
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit):0.5 millilitre
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- Two males and one female
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 to 72 hours
- Score:
- 0.56
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 to 72 hours
- Score:
- 0.22
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 1, 24, 48, & 72 hours
- Score:
- ca. 1.1
- Max. score:
- 8
- Reversibility:
- fully reversible within: 72 hours
- Irritant / corrosive response data:
- At the one hour observation following patch removal, well-defined erythema was observed at the treated sites. At the 24 hours observation, very slight oedema was also evident in one of the treated rabbits. Incidence and severity of irritation decreased over time. Corrosion data was not provided
- Other effects:
- All treated animals appeared active and healthy. Apart from dermal irritation, no other signs of gross toxicity, adverse pharmacologic effect or other abnormal behaviour were reported.
Any other information on results incl. tables
Following exposure to 1-tetradecene for 4 hours, well defined erythema was observed at the treated sites at the one hour observation period. At 24 hours observation one rabbit also exhibited very slight oedema. The overall incidence and severity of irritation decreased over time with the animals displaying no dermal irritation at 72 hours. The authors calculated a primary dermal irritation (PDII) index of 1.1 using the Draize skin scoring system.
Applicant's summary and conclusion
- Interpretation of results:
- other: Not classified under OECD; not irritating
- Remarks:
- Criteria used for interpretation of results: OECD GHS
- Conclusions:
- Based on a Primary Dermal Irritation Index of 1.1, the study author considered Amodrill 1410 was considered to be slightly irritating to the skin of rabbits; however, according to OECD GHS, the test material would not be considered irritating.
- Executive summary:
In a primary dermal irritation study, young adult New Zealand rabbits (two males and one female) were dermally exposed to 0.5 millilitre of undiluted Amodrill 1410 for 4 hours to 6 square centimetre section of skin. Animals were then observed for 3 days. Irritation was scored by the Draize method.
All three rabbits exhibited well-defined erythema 1 hour following patch removal. Very slight oedema was evident in one rabbit 24 hours post exposure and all animals were free of dermal irritation by 72 hours post exposure. No signs of gross toxicity, adverse pharmacological effects or abnormal behaviour were reported. The mean erythema was 0.56 averaged over 72 hours (24, 48, and 72 hours); the mean oedema was 0.22 averaged over 72 hours (24, 48, and 72 hours). Based on a Primary Dermal Irritation Index of 1.1, the study author considered Amodrill 1410 was considered to be slightly irritating to the skin of rabbits; however, according to OECD GHS, the test material would not be considered irritating.
This study received a Klimisch score of 1 and is classified as reliable without restriction because it is GLP compliant.
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