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EC number: 203-733-6 | CAS number: 110-05-4
- 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: Well-conducted GLP study performed according to established protocol. Test article is well characterized and a certificate of analysis is included in the report.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 998
- Report date:
- 1998
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Di-tert-butyl peroxide
- EC Number:
- 203-733-6
- EC Name:
- Di-tert-butyl peroxide
- Cas Number:
- 110-05-4
- Molecular formula:
- C8H18O2
- IUPAC Name:
- 2-(tert-butylperoxy)-2-methylpropane
- Details on test material:
- Di-tert-butyl peroxide, lot number 990-9801-124, was provided by Elf Atochem. The material is characterized as a colorless liquid; purity is given as 99.2.%.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Three animals were used as recommended by international guidelines. Animals were identified individually with a metal tag in the ear. On the day of treatment, the animals had a mean body weight of 2.4 +/- 0.1 kg. Animals were acclimated at least 5 days before the beginning of the study. Conditions in the animal room were as follows: temperature, 18 +/- 3 °C; relative humidity, 30 to 70%; light/dark cycle, 12 hr/12 hr; ventilations, approximately 12 cycles/hour of filtered, non-recycled air. Animals were housed individually in polystyrene cages. Each cage was equipped with a food container and a water bottle. During the study, the animals had free access to 112C pelleted diet. Drinking water filtered by a FG Millipore membrane (0.22 micron) was provided ad libitum.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- Doses of 0.5 ml were placed on a 6 cm2 dry gauze pad, which was then applied to the right flank (application for 4 hours) or the left flank (application for 3 minutes) of the animals.
- Duration of treatment / exposure:
- Three minutes (one animal) or four hours (three animals).
- Observation period:
- One hour, 24, 48 and 72 hours after removal of the dressing or until reversibility of cutaneous reactions.
- Number of animals:
- Three
- Details on study design:
- The test substance was evaluated in one animal in a first assay. The duration of exposure was 3 minutes on one flank and 4 hours on the other flank. Since the test substance was not irritant in this first assay, it was then applied for 4 hours to two other animals in a second assay. The test substance was used undiluted. Doses of 0.5 ml were placed on a 6 cm2 dry gauze pad, which was then applied to the right flank (application for 4 hours) or the left flank (application for 3 minutes) of the animals. The test substance and the gauze pad were held in contact with the skin by means of an adhesive hypoallergenic aerated semi-occlusive dression and a restraining bandage. The untreated skin sered as control No residual test substance was observed on removal of the dressing.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48 h
- Score:
- 0
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 72 h
- Score:
- 1.7
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritant / corrosive response data:
- After a 3-minute exposure (one animal), no cutaneous reactions were observed. After a 4-hour exposure (three animals), a very slight erythema (grade 1) was observed in one animal on day 1. A well-defined erythema (grade 2) was observed in the second animal between days 1 and 3, then a very slight erythema (grade 1) was noted on day 4. It was replaced by dryness ofthe skin from day 5 up to day 8. No cutaneous reactions were observed in the third animal.
- Other effects:
- None recorded.
Any other information on results incl. tables
Mean scores over 24, 48 and 72 hours for each animal were 0.0, 0.0 and 1.7 for erythema and 0.0, 0.0 and 0.0 for oedema.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Under our experimental conditions, the test substance PEROXYDE DE DI-t-BUTYLE (batch No. 990-9801-124) is non-irritant when applied topically to rabbits.
- Executive summary:
The potential of the test substance PEROXYDE DE DI-t-BUTYLE (batch No. 990-9801-124) to induce skin irritation was evaluated in rabbits according to OECD (No. 404, 17th July 1992) and EC (92/69/EEC, B.4, 31st July 1992) guidelines. After a 3 -minute exposure (one animal), no cutaneous reactions were observed. After a 4-hour exposure (three animals), a very slight erythema (grade 1) was observed in one animal on day 1. A well-defined erythema (grade 2) was observed in the second animal between days 1 and 3, then a very slight erythema (grade 1) was noted on day 4. It was replaced by dryness of the skin from day 5 up to day 8. No cutaneous reactions were observed in the third animal. Under our experimental conditions, the test substance PEROXYDE DE DI-t-BUTYLE (batch No. 990-9801-124) is non-irritant when applied topically to rabbits.
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