Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 204-340-2 | CAS number: 119-64-2
- 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
Two experimental in vivo studies with rabbits reported skin irritating effects for tetrahydronaphthalene (Hüls AG 1984, Carpenter 1949) also in a dermal toxicity study a skin irritating effect was observed in rats (Clark, 1984). Two experimental studies with rabbits showed no or mild and reversible eye irritation (Hüls AG 1984; Carpenter 1949).
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:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- Smyth HF Jr, Carpenter CP (1944): The place of the range finding test in the industrial toxicology laboratory. J. Ind. Hyg. Toxicol. 26, 269-273 and subsequent updates
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- not specified
- Type of coverage:
- not specified
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Amount / concentration applied:
- ADMINISTRATION/EXPOSURE
- Total volume applied: 0.01 ml
- undiluted - Duration of treatment / exposure:
- 24 hour(s)
- Number of animals:
- 5
- Details on study design:
- ADMINISTRATION/EXPOSURE
- Area of exposure: clipped belly
EXAMINATIONS
- Scoring system: Draize et al. (1944): Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous
membranes. J. Pharmacol. Exper. Therap. 82, 377; maximum scores: 10
- Examination time points: 24 hours after application - Irritation parameter:
- erythema score
- Basis:
- mean
- Score:
- 4
- Max. score:
- 10
- Remarks on result:
- other: moderate to marked erythema
- Other effects:
- Symptoms:
Moderate to marked erythema, intensity comparable to 2-ethyl hexyl acetate Irritation index: 4/10, where 4 is a slight erythema resulting of
exposure to an undiluted sample of the test substance. - Conclusions:
- Under the conditions of the study, Tetrahydronaphthalen was irritating to the skin.
- Executive summary:
The application of 0.01 mL of the undiluted tetrahydronaphthalene to the clipped skin of the rabbit produced moderate to marked erythema of an intensity comparable to that induced by 2 ethyl-hexylacetate which is representative of grade 4 compounds.
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- Test method used as described in the publication
- GLP compliance:
- not specified
- Species:
- rat
- Strain:
- Wistar
- Details on test animals or test system and environmental conditions:
- TEST ORGANISMS:
- Weight at study initiation: 225-306 g
- Strain: COBS/Wistar
- Sex: male - Type of coverage:
- open
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Amount / concentration applied:
- ADMINISTRATION:
- undiluted
- Vehicle: none
- Total volume applied: maximum 2.0 ml per rat - Duration of treatment / exposure:
- 24 h
- Number of animals:
- 2
- Details on study design:
- ADMINISTRATION:
- Area covered: shaved, approximately 20-25 % of body surface
- Occlusion: no
-undiluted - Irritation parameter:
- other: No irritation index provided
- Other effects:
- No irritation index provided
- Conclusions:
- Mild skin irritation was reported.
- Executive summary:
In an acute dermal toxicity test two male rats each received a dermal doses of 1.8 g, 3.6 g or 7.3 g Tetrahydronaphthaline applied undiluted to the shaved skin with unoccluded dressing for 24 h.
No adverse systemic effects were noted during 14 days observation period.
Local effects were summarised as mild skin irritation.
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1984-11-13 to 1984-11-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions: In deviation from OECD TG 404 occlusive dressing was used.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- other: Small white Russian, Chbb-SPF
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS:
- Strain: Small white Russian, Chbb-SPF
- Sex: male and female
- Source: Dr. Karl Thomae GmbH, Biberach, Germany
- Weight at study initiation: 2.2-2.5 kg
- Number of animals: 3 males, 3 females - Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- ADMINISTRATION/EXPOSURE
- Vehicle: none
- Total volume applied: 0.5 ml - Duration of treatment / exposure:
- 4 hour(s)
- Observation period:
- Postexposure period: 14 days
- Number of animals:
- 3 per sex
- Details on study design:
- ADMINISTRATION/EXPOSURE
- Area of exposure: 6 cm²
- Occlusion: mull patch, polyethylene film, elastic dressing
- Postexposure period: 14 days
- Removal of test substance: washing with warm water
EXAMINATIONS
- Scoring system: according to Draize
- Examination time points: 1, 24, 48, 72 hours, 6, 9, 11, and 14 days after administration of the test substance - Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 1, 24, 48, 72 h
- Score:
- 4.55
- Max. score:
- 8
- Reversibility:
- not fully reversible within: 14 days
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24-72 h
- Score:
- 3.11
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24-72 h
- Score:
- 1.56
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 14 days
- Conclusions:
- According to the outcome of the skin irritation study tetrahydronaphthalene is moderately irritant to skin of rabbits.
- Executive summary:
In a primary skin irritation test with three male and three female rabbits tetrahydronaphthalene was applied with occlusive dressing to the shaved back skin at a dose level of 0.5 mL per animal for 4 h. Residual test substance was washed of with warm water. Skin reaction were scored according to OECD criteria at 1h, 24h, 48h, 72h and 6d, 9d, 11d and 14d after application.
Referenceopen allclose all
Mild skin irritation was reported.
AVERAGE SCORE
- Erythema: 3.11
- Edema: 1.56
- Irritation index: 4.55/8 = moderately irritant
REVERSIBILITY: not complete within 14 days
Irritant response data for each animal at each observation time
Score at time point / Reversibility |
Erythema |
Edema |
Max. score: 4 |
Max. score: 4 |
|
60 min |
2/2/2/3/2/2 |
2/2/2/2/2/2 |
24 h |
3/3/3/3/3/3 |
1/3/2/2/1/1 |
48 h |
3/4/3/3/3/3 |
1/3/1/2/1/1 |
72 h |
3/4/3/3/3/3 |
2/3/1/1/1/1 |
6 days |
3/3/2/2/2/2 |
2/3/1/1/1/1 |
9 days |
Eschar formation for all animals |
|
11 days |
Eschar formation for all animals |
|
14 days |
Eschar formation for all animals |
|
Average 24h, 48h, 72h |
3.11 |
1.56 |
Reversibility |
Not completely reversible |
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
- Study period:
- 1984-11-13 to 1984-11-19
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Guideline study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- other: Small white Russian, Chbb-SPF
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS:
- Strain: Small white Russian, Chbb-SPF
- Sex: male and female
- Source: Dr. Karl Thomae GmbH, Biberach
- Weight at study initiation: 2.2-2.7 kg
- Number of animals: 3 males, 3 females - Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- - undiluted
- Amount applied: 0.1 ml
- Controls: untreated (left) eye - Duration of treatment / exposure:
- not rinsed
- Observation period (in vivo):
- Ophtalmoscopic examination: 1, 24, 48, 72 hours, 6 days after treatment
- Number of animals or in vitro replicates:
- 6
- Details on study design:
-
EXAMINATIONS
- Ophtalmoscopic examination: 1, 24, 48, 72 hours, 6 days after treatment
- Scoring system: Draize (1959); Appendix VI of 79/831/EEC
- Tool used to assess score: Na fluorescein / ophthalmic lamp / visual inspections - Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 5.17
- Max. score:
- 110
- Reversibility:
- fully reversible within: 6 days
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24,48, 72 h
- Score:
- 0
- Max. score:
- 80
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 0
- Max. score:
- 10
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 1.33
- Reversibility:
- fully reversible within: 6 days
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24, 48, 72 h
- Score:
- 0.22
- Reversibility:
- fully reversible within: 48 h
- Conclusions:
- The rabbits In the study showed only slight to mild but also reversible conjunctival effects. Tetrahydronaphthalene was not considered to be an eye irritant.
- Executive summary:
In a primary eye irritation study 0.1 mL of undiluted tetrahydronaphthalene was instilled into the conjunctival sac of one eye of three male and three female young adult White Russian rabbits. Eyes were not rinsed. Animals were observed for 6 days.
Cornea and iris were not affected. Slight to mild and reversible conjunctival effects were observed. In this study, tetrahydronaphthalene was not an eye irritant.
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
- Principles of method if other than guideline:
- Carpenter CP, Smyth HF (1946): Chemical burns of the rabbit cornea, Am. J. Ophthalmol. 29, 1363-1372
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- other: Albino
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS:
- Strain: Albino, not specified - Vehicle:
- unchanged (no vehicle)
- Amount / concentration applied:
- ADMINISTRATION/EXPOSURE
- Exposure period: 18 - 24 h
- undiluted
- Amount applied: 0.5 ml - Number of animals or in vitro replicates:
- 5
- Details on study design:
- Comment: not rinsed
EXAMINATIONS
- Scoring system: maximum 10 scores
- Tool used to assess score: eye examined in strong diffuse daylight, then stained with fluorescein - Irritation parameter:
- overall irritation score
- Score:
- 1
- Max. score:
- 10
- Reversibility:
- not specified
- Other effects:
- - Overall irritation score: 1
"No damage" - Conclusions:
- Under conditions of this study conducted with rabbits tetrahydronaphthalene is not considered to be an eye irritant.
- Executive summary:
In a primary eye irritation study 0.5 mL of undiluted tetrahydronaphthalene was instilled into the eye of albino rabbits. Animals were observed for 3 days.
Cornea and iris were not affected. Very mild and reversible conjunctival effects were observed. In this study, tetrahydronaphthalene was not an eye irritant..
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Cited from SIAR for19 (19-22 October 2004):
Skin irritation
Studies in Animals
In a study according to OECD TG 404 with rabbits (Small white Russian), undiluted 1,2,3,4-tetrahydronaphthalene caused moderate irritation with Draize scores of 3.11 for erythema, 1.56 for edema, and 4.55 in total. Effects were not completely reversible within 14 days (Hüls AG, 1984 b).
Similar irritation intensity was observed in an early and limited study published by Smyth, Carpenter and Weil (1951) as well as by Union Carbide Corp. (1992). They report an irritation index of 4/10 in rabbits 24 hours after application of 0.01 ml 1,2,3,4-tetrahydronaphthalene to the clipped belly of rabbits (no information on occlusion).
Studies in Humans
A skin condition similar to turpentine-induced dermatitis that was eczematous in nature is reported in five painters (four males, one female) that used 1,2,3,4-tetrahydronaphthalene (1 case) or mixtures containing 1,2,3,4-tetrahydronaphthalene as substitutes for turpentine. From the rare occurrence of the symptoms, the author concluded that the persons probably had a high sensitivity (Galewsky, 1922).
Eye Irritation
Studies in Animals
In a study according to OECD TG 405 with rabbits (Small white Russian), undiluted 1,2,3,4-tetrahydronaphthalene caused no significant irritation with Draize scores of 5.17/110. Effects were completely reversible within 6 days (Hüls AG, 1984 a). Similar irritation intensity was observed in an early study published by Smyth, Carpenter and Weil (1951) as well as by Union Carbide Corp. (1992). They report an irritation index of 1/10 in rabbits 18-24 hours after application of 0.5 ml 1,2,3,4-tetrahydronaphthalene to rabbits (not rinsed).
Studies in Humans
Two painters who had been painting for three days with 1,2,3,4-tetrahydronaphthalene-containing varnishes in a poorly ventilated area complained, among others, about irritation of mucous membranes and profuse lacrimation (Arnstein, 1922).
Respiratory Tract Irritation
There were no studies available in animals or humans
Conclusion
1,2,3,4-Tetrahydronaphthalene was a moderate irritant to the skin (OECD TG 404) but not to the eye (OECD TG 405). However, high exposure from the gas phase may cause irritation of mucous membranes and profuse lacrimation in humans.
Effects on skin irritation/corrosion: irritating
Justification for classification or non-classification
All available data for skin corrosion/irritation showed that tetrahydronaphthalene has to be classified as skin irritant. Based on our study data for eye irritation, tetrahydronaphthalene does not require classification and labelling as eye irritant (Hüls AG, 1984). However, according to classification according to Annex VI of CLP regulation 1272/2008, tetrahydronaphthalene was classified as eye irritant Cat. 2.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.