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EC number: 266-019-3 | CAS number: 65996-85-2 The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.
- 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 sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study is comparable to the Buehler test described in OECD Guideline 406 (adopted 1992) with acceptable restrictions (low number of animals, no negative control, low concentration of the test substance at challenge; partly limited documentation)
Data source
Reference
- Reference Type:
- publication
- Title:
- Sensitization potency of some phenolic compounds
- Author:
- Itoh M
- Year:
- 1 982
- Bibliographic source:
- J Dermatol 9: 223-233
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- yes
- Remarks:
- (no control group)
- GLP compliance:
- not specified
- Type of study:
- other: modified Buehler test
Test material
- Reference substance name:
- Phenol
- EC Number:
- 203-632-7
- EC Name:
- Phenol
- Cas Number:
- 108-95-2
- Molecular formula:
- C6H6O
- IUPAC Name:
- phenol
- Details on test material:
- commerciaJ phenol was used; purification by fractional distillation (b.p. 8O.4°C/15 mmHg); source: Shiono Koryo Kaisha, Ltd.; purity 99.9%.
No further data available
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- Albino, 350 to 400 g body weight at initiation. No further details given.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 10% phenol in petrolatum for induction
1 and 0.1% phenol in petrolatum for challenge
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 10% phenol in petrolatum for induction
1 and 0.1% phenol in petrolatum for challenge
- No. of animals per dose:
- 10
- Details on study design:
- Pilot study for determination of irritant concentration
10 females per concentration used. Hair on the flank was shaved and about 20 mg of 10, 5, 2, 1, 0.5 and 0.2% of phenol in white petrolatum applied in Finn chambers on Scanpor tape (Epitest Co., Ltd.); Finn chambers applied to the shaved flanks and cloth tape (Dermicel) wrapped around the bodies of animals; foam pads applied over the cloth tape and secured to the animals' flanks with additional cloth tape; Forty-eight hours after application, the test materials removed; readings 1, 24 and 48 hours after the removal of test materials.
Sensitization Tests
10 females were used.
Induction: nape hair shaved and about 50 mg of 10% phenol in white petrolatum applied to round cloth (1.5 cm in diameter) of Torii's patch plaster [adhesive plaster] and applied to the napes; Dermicel cloth tape, Reston foam pads, and then Dermicel cloth tape placed over the patch plaster; test materials removed 48 hours after application (in OECD guideline 406 an exposure duration of 6 hours is recommended).
This procedure was repeated three times a week for two weeks (in OECD guideline 406 totally 3 applications in 2 weeks are recommended).
Challenge: 2 weeks after the end of the induction procedure, the flanks of the guinea pigs were shaved; 1% and 0.1% phenol (presumably both concentrations tested in the same group) in white petrolatum (presumably 50 mg) occluded with Finn chambers on Scanpor on the shaved flank areas (no further data). Further dressing in the same manner as for induction; test material removed 48 hours after application; degree of reaction determined 1, 24, 48 hours and one week after removal of the test material. - Challenge controls:
- no negative control
- Positive control substance(s):
- yes
- Remarks:
- (in parallel trials with other phenolic substances clearly positive results were obtained)
Study design: in vivo (LLNA)
- Positive control substance(s):
- other: e.g. isoeugenol
- Statistics:
- No data
Results and discussion
- Positive control results:
- isoeugenol: positive results in 16 out of 20 animals in parallel experiments
In vivo (non-LLNA)
Results
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 1 or 0.1%
- No. with + reactions:
- 0
- Total no. in group:
- 9
- Clinical observations:
- no data
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 1 or 0.1%. No with. + reactions: 0.0. Total no. in groups: 9.0. Clinical observations: no data.
Any other information on results incl. tables
Pilot test
Only 10% phenol in petrolatum (highest concentration tested) resulted in irritant effects in 9 out of 10 animals. No further details were given.
Sensitization test
Only data 24 h after removal were presented in a table. Results 1, 48 hours and one week after application were not documented but negative results are presumed.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information
- Conclusions:
- Phenol has no sensitizing properties in the modified Buehler test.
- Executive summary:
The study is comparable to the Buehler test described in OECD Guideline 406 (adopted 1992) with acceptable restrictions (low number of animals, no negative control, low concentration of the test substance at challenge; partly limited documentation).
The author used a modified Buehler test. Ten female guinea pigs received for induction semiocclusive patches with 50 mg of 10% phenol in white petrolatum (irritant concentration in a pilot study). This procedure was repeated three times a week for two weeks. Two weeks after the end of the induction procedure guinea pigs received for challenge occlusive patches with 1% and 0.1% phenol and test material was removed 48 hours after application; degree of reaction was evaluated 1, 24, 48 hours and one week after removal of the test material. No positive reaction was detected in 9 animals but in a parallel positive control group (isoeugenol: 16/20 animals positive).
Conclusion: Phenol has no sensitizing properties in the modified Buehler test.
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