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EC number: 700-954-4 | CAS number: 1338-23-4
- 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: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- Deviations:
- yes
- Remarks:
- see below
- Principles of method if other than guideline:
- Thirty male rats of Charles River CD strain, weighting 200 to 260 grams, were divided equally into 6 groups. Single, oral doses of the test material, suspended in corn oil, were administered to rats that were fasted overnight. Observations for mortality were recorded daily for 14 days.
- GLP compliance:
- not specified
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Reference substance name:
- 2-[(2-hydroperoxybutan-2-yl)peroxy]butane-2-peroxol; butane-2,2-diperoxol
- EC Number:
- 700-954-4
- Cas Number:
- 1338-23-4
- Molecular formula:
- Mixture of C4H10O4 and C8H18O6
- IUPAC Name:
- 2-[(2-hydroperoxybutan-2-yl)peroxy]butane-2-peroxol; butane-2,2-diperoxol
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Charles River CD
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 200 to 260 g
- Fasting period before study: fasting overnight
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- corn oil
- Doses:
- 508.1, 807.1, 1281, 2034, 3229, 5126 mg/kg bw
- No. of animals per sex per dose:
- 5 male rats per dose
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Necropsy of survivors performed: no
- Other examinations performed: body weight
Results and discussion
Effect levels
- Key result
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 1 017 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 879 - <= 1 175
- Mortality:
- No mortality was shown up to doses level 807.1 mg/kg bw. All other animals were dead up to days 1. Details see in the field "Any other information on results incl. tables".
Any other information on results incl. tables
Dose levels (mg/kg bw) |
Number of dead animals |
Total moralities |
hours |
days |
508.1 |
0/4 |
|
|
|
807.1 |
0/5 |
|
|
|
1281 |
0/5 |
|
|
|
2034 |
5/5 |
|
|
|
3229 |
5/5 |
|
|
|
5126 |
5/5 |
|
|
|
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- The acute oral toxicity (LD50) value for methyl-ethylketone peroxide in DMP in male albino rats was calculated to be 1017 (879 - 1175) mg/kg.
- Executive summary:
Methyl-ethylketone peroxide in DMP was tested in an acute oral toxicity study to thirty male rats of Charles River CD strain.
The thirty animals were divided equally into 6 groups. Single, oral doses of the test material, suspended in corn oil, were administered to rats that were fasted overnight. Observations for mortality were recorded daily for 14 days.
The acute oral toxicity (LD50) value for methyl-ethylketone peroxide in male albino rats was calculated to be 1017 (879 - 1175) mg/kg .
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