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EC number: 701-339-3 | CAS number: -
- 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: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Only available as a brief summary report
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- In an acute dermal toxicity study, the test material was applied to the skin of rabbits at two doses, and animals assessed for toxic symptoms.
- GLP compliance:
- not specified
- Test type:
- other:
- Limit test:
- no
Test material
- Reference substance name:
- 1,2-Benzenedicarboxylic acid, benzyl isononyl alkyl esters
- EC Number:
- 701-339-3
- Cas Number:
- 68515-40-2
- Molecular formula:
- C24H30O4
- IUPAC Name:
- 1,2-Benzenedicarboxylic acid, benzyl isononyl alkyl esters
- Details on test material:
- Name of test material (as cited in study report): Santicizer 261
- Lot/batch No.: DE 114
no further data
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 2.2-2.5 kg
no further data
Administration / exposure
- Type of coverage:
- not specified
- Vehicle:
- unchanged (no vehicle)
- Duration of exposure:
- 24 hours
- Doses:
- 5.01 and 7.94 g/kg bw
- No. of animals per sex per dose:
- One male was tested at 5.01 g/kg bw, and one male and one female at 7.94 g/kg bw
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, macroscopic evaluation
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 7 940 mg/kg bw
- Remarks on result:
- other: No deaths at 7.94 g/kg bw
- Mortality:
- All three animals survived the 14-day observation period
- Clinical signs:
- other: Reduced appetite and activity seen for one to three days (number of animals and doses not given)
- Gross pathology:
- The viscera appeared normal following macroscopic examination
Applicant's summary and conclusion
- Interpretation of results:
- other: Not classified
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- There were no deaths when three rabbits (mixed sex) were given a 24-hour skin application of undiluted Santicizer 261 at up to 7.94 g/kg bw and then observed for two weeks.
- Executive summary:
Undiluted Santicizer 261 was applied to the skin of a total of three New Zealand white rabbits. One male was dosed at each of 5.01 and 7.94 g/kg bw, and one female dosed at 7.94 g/kg bw, for an exposure period of 24 hours. The animals were assessed for toxic symptoms during the observation period, and the surviving animals sacrificed 14 days after dosing and examined macroscopically.
All three animals survived the 14-day observation period. Reduced appetite and activity was seen for one to three days (no details on number of animals or doses given). At necropsy, the viscera appeared normal. The investigators concluded that the LD50 was greater than 7.94 g/kg bw. Under the EU CLP regulations, this study would indicate that Santicizer 261 is not classified for acute dermal toxicity.
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