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EC number: 410-190-0 | CAS number: 132983-41-6 MCP 968
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented study report similar or equivalent to OECD 404. GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- multiple test sites per animal, including abraded test sites and occluded sites. 4h exposure was occluded
- GLP compliance:
- yes
Test material
- Reference substance name:
- A mixture of isomers of: mono-(2-tetradecyl)naphthalenes; di-(2-tetradecyl)naphthalenes; tri-(2-tetradecyl)naphthalenes
- EC Number:
- 410-190-0
- EC Name:
- A mixture of isomers of: mono-(2-tetradecyl)naphthalenes; di-(2-tetradecyl)naphthalenes; tri-(2-tetradecyl)naphthalenes
- Cas Number:
- 132983-41-6
- Molecular formula:
- Can vary from C24H36 (mono rxn product) to C52H92 (tri rxn product)
- IUPAC Name:
- 2,3,6-tritetradecylnaphthalene; 2,3-ditetradecylnaphthalene; 2-tetradecylnaphthalene
- Details on test material:
- MCP 968 is a straw colored homogenous liquid. The MEHSL CRU number is 90163. This substance is stable for 6 month at 20C with an expiration date of 8/30/1990.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Three male and three female young adult New Zealand White rabbits obtained form Hazleton Research Products, Inc. (Denver, Pa) were used in this study. The animals were identified by individual ear tags and cage cards. The temperature of the study room was maintained at 68-71F with a relative humidity of 44-66%
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- other: intact and abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- 0.5ml
- Duration of treatment / exposure:
- 4-hour (occluded) and 24 hours (occluded and non-occluded)
- Observation period:
- Following the 4 hour exposure, the test sites were evaluated for dermal irritation at 4.5, 28, 52, and 76 hours. Following the 24 hour exposure, clinical observations were recorded at approximately 1 and 4 hours post-dosing and the sites were evaluated for dermal irritation at 26 and 72 hours post-exposure.
- Number of animals:
- 6 animals (3/sex).
- Details on study design:
- Three 1 sq. in. test sites were selected on both the left and right flank of each animal and designated as anterior (4-hour, occlusion), middle (24-hour occlusion), and posterior (24-hour, no occlusion). All sites on the right flank were abraded prior to administration prior to administration of the test substance. 0.5mls of the test substance was applied to the anterior and middle test sites under Webril patches. The patches were secured with an occlusive rubber dam followed by a non-irritating surgical tape. 0.5mls of the test substance was also applied to the posterior test sites without occlusion. Elizabethan style collars were fitted to each animal after administration of the test substance. Following a 4 hour exposure the anterior sites were unwrapped and evaluated fro dermal corrosion. The residual test substance was wiped from the test sites and the sites reevaluated fro corrosion 48 hours post-dosing. The test sites were also evaluated for dermal irritation at 4.5, 28, 52, 76 hours according to the Draize method.
Following a 24 hour exposure period the middle test sites were unwrapped and the residual test substance wiped from both the middle and posterior test sites. These sites were evaluated for dermal irritation at 26 and 72 hours according to the Draize method. Clinical observations were recorded at approximately 1 and 4 hours post-dosing and daily thereafter. T he condition of each animal (live, dead, moribund) was checked daily in the morning.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24h
- Score:
- 0
- Remarks on result:
- other: 4hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 48h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72 hrs
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Remarks:
- combined mean
- Basis:
- mean
- Time point:
- other: 24/48/72 hr average
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 hrs
- Score:
- 0.2
- Reversibility:
- fully reversible
- Remarks:
- by 48 hours
- Remarks on result:
- other: 4 hour occluded exposure
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 48 hrs
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72 hrs
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Remarks:
- combined mean
- Basis:
- mean
- Time point:
- other: 24/48/72 hr average
- Score:
- ca. 0.07
- Max. score:
- 0.2
- Reversibility:
- fully reversible within: 48 hours
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #5
- Time point:
- 24 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #6
- Time point:
- 24 h
- Score:
- 1
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #5
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #6
- Time point:
- 48 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #5
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Irritation parameter:
- edema score
- Basis:
- animal #6
- Time point:
- 72 h
- Score:
- 0
- Remarks on result:
- other: 4 hr occluded exposure
- Other effects:
- 4 hour exposure of abraded skin under occlusive conditions resulted in a combined erythema mean of 0.2 and a combined edema mean of 0.23. Evidence of erythema and edema were reported at all time points. Neither edema nor erythema were fully reversible within the 72 hour timepoint.
24 hour exposure under occluded conditions of unabraded skin resulted in erythema scores of 0.3 and 0 at 24 and 72 hours respectively, and edema scores of 0.5 and 0 at 24 and 72 hours respectively. Under semiocclusive conditions, 24 hour exposure to unabraded skin resulted in erythema and edema scores of 0 at 24 and 72 hours.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The mean erythema and edema scores for the test material were 0 and 0.07 (4 hour occluded).This finding does not warrant classification of the test material as a dermal irritant under the new Regulation (EC) 1272/2008 on classification, labeling, and packaging of substances and mixtures (CLP) nor as an R38 skin irritant under the Directive 67/518/EEC for dangerous substances and Directive 1999/45/EC for preparations.
- Executive summary:
The test material was administered to the skin of New Zealand White rabbits. Test sites were selected on both the left and right flank of each animals and designated as anterior (4-hour, occluded), middle (24-hour, occluded), and posterior (24-hour, non-occluded). All sites of the right flank were abraded. 0.5 ml of the test substance was applied to each test site. Following the 4 hour exposure, the test sites were evaluated for dermal irritation at 1/2, 24, 48, and 72 hours according to the Draize method. Following the 24 hour exposures, both test sites were evaluated at 26 and 72 hours. Clinical observations were recorded at approximately 1 and 4 hours post-dosing. Soft stool, decreased fecal output, and decreased food consumption were observed in one or more animals. The mean erythema and edema scores for the test material on unabraded skin were 0 and 0.7 (4 hour occluded), 0.15 and 0.25 (24 hour occluded), and 0 and 0 (24 hour non-occluded), respectively.This finding does not warrant classification of the test material as a dermal irritant under the new Regulation (EC) 1272/2008 on classification, labeling, and packaging of substances and mixtures (CLP) nor as an R38 skin irritant under the Directive 67/518/EEC for dangerous substances and Directive 1999/45/EC for preparations.
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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