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EC number: 216-644-2 | CAS number: 1633-22-3
- 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
- Study period:
- 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 402 (Acute Dermal Toxicity)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Dichlorotricyclo[8.2.2.24,7]hexadeca-1(12),4,6,10,13,15-hexaene, mixed isomers
- EC Number:
- 249-236-8
- EC Name:
- Dichlorotricyclo[8.2.2.24,7]hexadeca-1(12),4,6,10,13,15-hexaene, mixed isomers
- Cas Number:
- 28804-46-8
- Molecular formula:
- C16H14Cl2
- IUPAC Name:
- Unknown constituents
- Test material form:
- solid: granular
1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- 5 males and 5 females
Administration / exposure
- Vehicle:
- other: pulverised and moistened with 0.2 mL freshly collected RO water
- Details on dermal exposure:
- The test item was held in contact with the skin using porous gauze dressing and a non-irritating tape throughout the 24 h exposure period.
- Duration of exposure:
- 24 h
- Doses:
- 2000 mg/kg bw
- No. of animals per sex per dose:
- 5 males and 5 females/2000 mg/kg bw
Results and discussion
Effect levels
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Mortality:
- No mortality was observed in rats treated with 2000 mg DPX-C (Di-Cloro-Di-p-Xililene)/kg body weight.
- Clinical signs:
- No treatment related clinical signs were observed in any of the rats treated with 2000 mg DPX-C (Di-Cloro-Di-p-Xililene)/kg body weight.
- Body weight:
- All the male rats showed no appreciable change in mean body weight while decrease in the mean body weight was observed in female rats on day 7 which was increased on day 14 when compared to day 0 mean body weight treated with 2000 mg DPX-C (Di-Cloro-Di-p-Xililene)/kg body weight.
- Gross pathology:
- External
External examination of terminally sacrificed rats did not reveal any abnormality.
Internal
Visceral examination of terminally sacrificed rats did not reveal any lesion.
In the absence of any lesion in terminally sacrificed rats, it is concluded that the test item did not produce any treatment related effect at the dose level used in the present study.
Applicant's summary and conclusion
- Interpretation of results:
- other: Category 5 or Unclassified (GHS 2015)
- Conclusions:
- No mortality was observed following dermal application of 2000 mg DPX-C (Di-Cloro-Di-p-Xililene)/kg body weight. The acute dermal LD50 of DPX-C (Di-Cloro-Di-p-Xililene) in Wistar male and female rats was found to be greater than 2000 mg/kg body weight.
- Executive summary:
In an acute dermal toxicity study, a group of 8 to 13 weeks old Wistar rats (5 males and 5 females) was dermally exposed toDPX-C (Di-Cloro-Di-p-Xililene)for 24 h following applicationat a limit dose of 2000 mg/kg body weight. The required amount (506.8 to 598.6 mg) ofDPX-C (Di-Cloro-Di-p-Xililene)(pulverised and moistened with 0.2 mL freshly collected RO water)was applied over the clipped area (approximately7 × 5 cm body surface area) and the rats were observed for a period of 14 days.
There were no treatment-related mortality, clinical signs and necropsy findings recorded.
All the male rats showed no appreciable change in mean body weight while decrease in the mean body weight was observed in female rats on day 7 which was increased on day 14 when compared to day 0 mean body weight treated with 2000 mg DPX-C (Di-Cloro-Di-p-Xililene)/kg body weight.
The acute dermal median lethal dose (LD50) ofDPX-C (Di-Cloro-Di-p-Xililene)in Wistar rats (males and females) was found to be greater than 2000 mg/kg body weight.
Based on the results of this study, an indication of the classificationforDPX-C (Di-Cloro-Di-p-Xililene)isas follows:
Globally Harmonized System of Classification and Labelling of Chemicals (GHS 2015): Category 5 or Unclassified.
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