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EC number: 203-252-1 | CAS number: 104-92-7
- 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
- Study period:
- 21 Oct. 1996 -21 Nov. 1996
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 997
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
Test material
- Reference substance name:
- 4-bromoanisole
- EC Number:
- 203-252-1
- EC Name:
- 4-bromoanisole
- Cas Number:
- 104-92-7
- Molecular formula:
- C7H7BrO
- IUPAC Name:
- 1-bromo-4-methoxybenzene
- Details on test material:
- 98.75% purity
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
- Source:David Hall Limited, Burton-on-Trent, Staffordshire, UK.
Females: nulliparous and non-pregnant.
- Age at study initiation: 8-12 weeks old.
- Weight at study initiation: 307- 379 g
- Housing: singly or in pairs in solid-floor polypropylene cages furnished with woodflakes.
- Diet : Animals had free access to food (Guinea Pig FD1 Diet, Special Diets Services Limited, Witham, Essex, UK)
- Water : Animals had free access to drinking water.
- Acclimation period: At least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18-32 ºC
- Humidity (%): 37 to 64 %
- Air changes (per hr): 15 changes per hour.
- Photoperiod (hrs dark / hrs light): 12/12
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal
- Vehicle:
- arachis oil
- Concentration / amount:
- For Intradermal induction: 1, 5, 10 and 25 % w/v (the prelimiary study).
For Topical induction: 75, 50 and 25 % v/v (the prelimiary study).
For Topical challenge: 25, 50 and 75 % v/v
Challengeopen allclose all
- Route:
- epicutaneous, occlusive
- Vehicle:
- arachis oil
- Concentration / amount:
- For Intradermal induction: 1, 5, 10 and 25 % w/v (the prelimiary study).
For Topical induction: 75, 50 and 25 % v/v (the prelimiary study).
For Topical challenge: 25, 50 and 75 % v/v
- No. of animals per dose:
- 20 test and 10 control.
- Details on study design:
- RANGE FINDING TESTS:
A preliminary test was performed to determine the concentration to be used in the main study.
By intradermal route:
Determination of Maximum Non-Irritant Concentration (M.N.I.C.)
- On day 0 before treatment, the shoulder region was clipped.
- the test substance was prepared in an appropriate vehicle,
- intradermal administration of the test substance (volume 0.1 ml) at increasing concentrations was performed in order to determine the minimum
concentration which causes mild to moderate irritation,
- evaluation of the potential cutaneous reactions, 24 and 48 hours after injection.
By topical route:
Determination of Maximum Non-Irritant Concentration (M.N.I.C.):
- Shoulder region of the animals was clipped again after 1 week (after the intradermal injection)
- Topical administration of the test substance undiluted at increasing concentrations was applied performed in order to determine the minimum
concentration which causes mild to moderate irritation undiluted was applied to a filter paper patch of approximately 40 mmx20 mm and then held in place by an occlusive dressing of strip of surgical adhesive tape covered by an overlapping length of aluminium foil that also were secured with a
strip of elastic adhesive bandage wound in a double layer around the torso of each animal for 48 hours,
- potential cutaneous reactions were evaluated 1 and 24 hours after removal of the pads.
MAIN STUDY
A. INDUCTION EXPOSURE
Intradermal route:
On day 0, intradermal injections were made into a clipped area (4 cm x 6 cm) in the shoulder region. Three injections of 0.1 ml were injected into
each side of the mid-line of animal, as follows:
Control group:
• Freund's complete adjuvant plus distilled water in the ratio 1:1
• Vehicle,
• A 50% w/v formulation of vehicle in Freund's Complete Adjuvant/distilled water 1:1
Treated group:
• Freund's complete adjuvant plus distilled water in the ratio 1:1
• A 10% w/v solution of the test substance in the vehicle,
• A 10% w/v emultion of the test material in a 1:1 preparation of Freund's Complete Adjuvant plus distilled water
Topical route:
On day 7, the shoulder area was clipped again. The test substance was held in place with a strip of surgical adhesive tape covered with an overlapping length of aluminium foil and further secured with a strip of elastic adhesive bandage wound.
Control group:
• Nothing was applied to the filter paper.
Treated group:
• Application of the undiluted test substance.
The test substance and the vehicle were prepared on a dry gauze pad, which was then applied to the region and held in place for 48 hours by means
of an adhesive dressing.
The degree of erythema and oedema was evaluated 1 and 24 hr after dressing removal.
B. CHALLENGE EXPOSURE
At the end of the test period on day 21, the test substance was applied at the Maximum Non-Irritant Concentration (M.N.I.C.) i.e.
in its original form and one lower concentration.
On day 21, 2 animals received an application of the M.N.I.C. of the test substance and one lower concentration on the clipped flanks under occlusive
dressings for an exposure period of 24 hr.
The test substance was applied on a patch, then applied to the shorn clipped area of the skin. The gauze pad was held in place with a strip of surgical adhesive tape. The patched were occluded with an overlapping bandage wound in a double layer around the torso of each animal.
After 24 hours, the dressing was cut. The chllenge sites were swabbed with cotton wool soaked in diethyl ether.
24 and 48 hours after challenge dressing removal, the degree of erythema and oedema was quantified.
Any other reactions were also recorded.
- Positive control substance(s):
- no
Study design: in vivo (LLNA)
- Statistics:
- % of animals showing a reaction Classification
0 Non-sensitiser
1-8 Weak sensitiser
9 - 28 Mild sensitiser
29 - 64 Moderate sensitiser
65 - 80 Strong sensitiser
81 - 100 Extreme sensitiser
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 50%. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 75%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 75%. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0% of test substance
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: negative control. Dose level: 0% of test substance. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 50%. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 75%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 75%. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: negative control. Dose level: 0% . No with. + reactions: 0.0. Total no. in groups: 10.0.
Any other information on results incl. tables
No skin reactions were noted at the challenge sites of the test or control group animals at the 24 or 48 -hour observations.
Applicant's summary and conclusion
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Under experimental conditions and according to the maximization method of Magnusson and Kligman, no cutaneous reactions possibly attributable
to the sensitization potential of the test substance, p-Bromoanisole, in its original form were observed in guinea-pigs - Executive summary:
A skin sensitization study according to the maximisation method of Magnusson and Kligman was performed on female Dunkin-Hartley guinea-pigs weighing 307 -379 g. The study was performed using the test substance p-Bromoanisole and in accordance with OECD 406 and to GLP standard.
No cutaneous reactions possibly attributable to the sensitization potential of the test substance were observed and the material is therefore not classified as a sensitizer.
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