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Diss Factsheets
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EC number: 236-050-7 | CAS number: 13122-18-4
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.2 (Acute Toxicity (Inhalation))
- GLP compliance:
- no
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Reference substance name:
- tert-butyl 3,5,5-trimethylperoxyhexanoate
- EC Number:
- 236-050-7
- EC Name:
- tert-butyl 3,5,5-trimethylperoxyhexanoate
- Cas Number:
- 13122-18-4
- Molecular formula:
- C13H26O3
- IUPAC Name:
- tert-butyl 3,5,5-trimethylhexaneperoxoate
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Central Institute for the Breeding of Laboratory Animals TNO, Zeist, The Netherlands
- Age at study initiation: Young adult
- Weight at study initiation: Males: about 235 g, females: about 160 g
- Housing: stainless steel/ glass exposure chamber; five male and five female rats in separate wire screen cages
Administration / exposure
- Route of administration:
- inhalation: mist
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: stainless steel/ glass aerodynamic nozzle nebulizer
- Exposure chamber volume: 1.5 m3
- Airflow rate: 3 m3/ h
TEST ATMOSPHERE
- Brief description of analytical method used: Samples of the atmosphere were drawn through a Bergshoeff air-sampler filled with xylene and subsequently analysed by gas-liquid chromatography with the aid of an Intersmat gaschromatograph with a QF-1 (4.8% diglycerol on a chromosorb G-AW-DMCS) stainless-steel column.
- Samples taken from breathing zone: yes - Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 4 h
- Concentrations:
- No data
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Necropsy of survivors performed: no - Statistics:
- not performed
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 0.8 mg/L air
- Exp. duration:
- 4 h
- Mortality:
- No mortality occurred
- Other findings:
- During the first half hour of the exposure period the rats were somewhat restless. This symptom gradually disappeared and after one hour all rats were asleep. This situation continued throughout the remainder of the exposure period.
Since no mortality occurred during the 4 hours of the exposure and the subsequent observation period, the 4 hour LC 50 could not be determined.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Conclusions:
- The results of the present acute inhalation study lead to the conclusion that the 4-hour LC 50 of tert-Butylperoxy-3,5,5-trimethylhexanoat is higher than 0.8 mg/L of air.
- Executive summary:
The acute inhalation toxicity of tert-Butylperoxy-3,5,5-trimethylhexanoat was studied by exposing rats for 4 hours to an aerosol of the undiluted substance at a concentration of 0.8 mg/L of air.
No mortality occurred and no signs of intoxication were observed.
It was concluded that the 4 -hour LC 50 of tert-butyl 3,5,5-trimethylperoxyhexanoate was higher than 0.8 mg/L of air.
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