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EC number: 202-653-9 | CAS number: 98-29-3
- 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:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Academic study, well documented, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Simultaneous p-tert-butylphenol-formaldehyde resin and p-tert-butylcatechol contact allergies in man and sensitizing capacities of p-tert-butylphenol and p-tert-butylcatechol in guinea pigs.
- Author:
- Zimerson E, Bruze M, Goossens A
- Year:
- 1 999
- Bibliographic source:
- J Occupational Environmental Medicine, 41(1), 23-28
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- not specified
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- This study has been performed before the LLNA study and since it is a publication it is publicly available.
Test material
- Reference substance name:
- 4-tert-butylpyrocatechol
- EC Number:
- 202-653-9
- EC Name:
- 4-tert-butylpyrocatechol
- Cas Number:
- 98-29-3
- Molecular formula:
- C10H14O2
- IUPAC Name:
- 4-tert-butylbenzene-1,2-diol
- Details on test material:
- p-tert-butylcatechol (TBC) 99%, manufactured by Acros Organics (Geel, Belgium).
TBC was showed to be of high purity, and the highest possible contamination of this substance with the monomers of PTBP-F-R, 2-MPTBP and 2,6-MPTBP, was lower than 0.02% and 0.01% w/w, respectively.
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS:
- Strain: Dunkin-Hartley
- Sex: female
- Source: J.A. Sahlin, Malmö, Sweden
- Age at study initiation: no data
- Weight at study initiation: 300-400 g
- Acclimation period: no data
- Housing: no data
- Diet: no data
- Water: no data
ENVIRONMENTAL CONDITIONS
- Temperature (degrees C): no data
- Humidity (%): no data
- Air changes: no data
- Photoperiod: no data
In life dates: no data
Study design: in vivo (non-LLNA)
Induction
- Route:
- other: intradermal and topical
- Vehicle:
- other: propylene glycol/acetone 90/10% v/v (intradermal)
Challenge
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: propylene glycol/acetone 90/10% v/v (intradermal)
- No. of animals per dose:
- 24: test group
12: control group - Details on study design:
- TOPICAL IRRITANCY:
It was studied by means of a 48-h closed patch test in 4-8 animals on the flank. Testing was performed 1 week after pretreatment of the animals with Freund's complete adjuvant (FCA).
INDUCTION / CHALLENGE SCHEDULE:
* Induction procedure:
For intradermal sensitisation, 3 injections were given in a row on each side of the shoulder: (I) 0.1 mL of FCA in water 50% v/v; (II)0.1 mL of TBC in propylene glycol/acetone 90/10% v/v; (III) 0.1 mL of a preparation consisting of a mixture of TBC and FCA in propylene glycol/acetone 90/10% v/v in which the concentration for FCA was the same as that in (I) and the concentration of TBC was the same as that in (II).
24h before the topical sensitisation, all animals were treated on 2x4 cm area on the shoulder with 200 µL of a preparation consisting of sodium lauryl sulphate 10% w/v in dimethylacetamide/acetone/ethanol 4/3/3 v/v/v.
Topical sensitisation on the same skin area was then performed with 20 µL of a solution of 16.7% TBC on a 2x4 cm patch of Munktell 1002 filter paper.
The patch was covered with overlapping, impermeable plastic adhesive tape. This in turn was firmly secured by adhesive bandage. The dressing was left in place for 48h.
* Challenge procedure:
Challenge I was performed 2 weeks after the end of the induction stage, and a 24-h occluded patch test was performed on the right flank with 25 µL of TBC 7.5% (w/v) on each of the 2 patches near the back.
The Al-test on Durapore was used for patch-testing and was firmly secured by Acrylastic and an outer layer of Durapore.
12 test animals received TBC on both patches; 6 test animals received TBC only on the cranially located patch, while the vehicle alone was applied to the other patch. 6 other test animals received the vehicle alone on the cranially located patch, while TBC was applied to the other patch.
Challenge II was performed at the same time as challenge I but on the left side of the flank. 6 patches were tested on 24 test and 12 control animals: 2 patches near the back, 2 near the abdomen, and 2 between the back and the abdomen. The animals were challenged with the sensitiser (TBC: 10%).
A challenge was performed with nonirritant solutions.
GRADING SYSTEM:
The reactions were evaluated in a blind manner 24h after the removal of the patches.
The minimal criterion of an allergic (positive) reaction was a confluent erythema. The number of positive animals in each test group was statistically compared with the number of positive animals in the corresponding control group and also with the number of positive test animals tested with the vehicle alone.
When both comparisons yielded significant values, the compound was considered to be a contact sensitiser.
For challenge II, a comparison was only made between the number of animals positive for each substance in the test and control groups. - Challenge controls:
- Challenge I & II: 12 females
no more data available - Positive control substance(s):
- yes
- Remarks:
- 2-methylol phenol
Results and discussion
- Positive control results:
- Challenge I: 3/6 positive animals
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 7.5 %
- No. with + reactions:
- 20
- Total no. in group:
- 24
- Clinical observations:
- No data
- Remarks on result:
- positive indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 10%
- No. with + reactions:
- 2
- Total no. in group:
- 12
- Clinical observations:
- No data
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- No data.
- No. with + reactions:
- 3
- Total no. in group:
- 6
- Clinical observations:
- No data
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 10%
- No. with + reactions:
- 18
- Total no. in group:
- 24
- Clinical observations:
- No data
- Remarks on result:
- positive indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- No data
- No. with + reactions:
- 1
- Total no. in group:
- 12
- Clinical observations:
- No data
Any other information on results incl. tables
CHALLENGE I:
Group Number of positive animals
Negative control/vehicle 2/12
TBC (7.5%) 20/24
CHALLENGE II:
Nb positive animals after challenge
Challenge substance TBC group (10%) Control group
TBC 18/24 1/12
Applicant's summary and conclusion
- Interpretation of results:
- Category 1 (skin sensitising) based on GHS criteria
- Conclusions:
- In this study, TBC was shown to be a potent sensitizer in guinea pigs.
EU GHS classification: skin sensitisation Category 1 (H317) - Executive summary:
In a dermal sensitization study using the method of Maximization test (Zimerson et al., 1999) with 4 -tert-butylpyrocatechol (TBC) in propylene glycol / acetone (90/10%), Dunkin-Hartley guinea pigs (24 females) were tested under test conditions similar to the guideline OECD 406. The positive control group received 2 -methylol phenol.
On day 1, three intradermal injections were performed in a row on each side of the shoulder. 24 hours before the topical sensitization (day 7), all the animals were treated on the shoulder with a preparation consisting of sodium lauryl sulphate (SLS) 10% in dimethyl acetamide/acetone/ethanol. On day 8, topical sensitization on the same skin area was then performed with a solution of the suspected sensitizer. The patch was covered by an occlusive dressing for 48 hours. On day 22 (= Challenge I), a 24 -hour occluded patch was performed on the right flank with 25µl of TBC, 2 patches near the back. Challenge II was performed at the same time as challenge I but on the left side of the flank.
The concentrations used for induction phase were 3.40% (intradermal) and 16.7% (topical) and those used for challenge phase were 7.50% (challenge I) and 10% (challenge II).
In challenge I, 20/24 treated animals showed positive reactions. In challenge II, 18/24 treated animals showed positive reactions.
In this study, 4 -tert-butylpyrocatechol was a dermal sensitizer.
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