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EC number: 204-077-3 | CAS number: 115-27-5
- 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:
- other: Study undertaken and reported scientifically but not to GLP.
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:
- OECD Guideline 433 draft (Acute Inhalation Toxicity: Fixed Concentration Procedure) (not officially approved)
- Deviations:
- not specified
- GLP compliance:
- no
- Test type:
- fixed concentration procedure
Test material
- Reference substance name:
- 1,4,5,6,7,7-hexachloro-8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride
- EC Number:
- 204-077-3
- EC Name:
- 1,4,5,6,7,7-hexachloro-8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride
- Cas Number:
- 115-27-5
- Molecular formula:
- C9H2Cl6O3
- IUPAC Name:
- 1,4,5,6,7,7-hexachloro-8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride
- Details on test material:
- - Name of test material (as cited in study report): Chlorendic anhydride- Physical state: Fine white powder containing some chunks.- Analytical purity: 93.8%- Lot/batch No.: 3-12-206
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: CD
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS- Source: Charles River- Age at study initiation: - Weight at study initiation: males, 211 to 226 g; female, 213 to 232 g- Fasting period before study: No- Housing: Wire-mesh cages.- Diet: Purina laboratory chow, ad libitum - Water: ad libitum- Acclimation period: 1 weekENVIRONMENTAL CONDITIONS- Temperature (°C): - Humidity (%): - Air changes (per hr): - Photoperiod (hrs dark / hrs light): IN-LIFE DATES: From: To:
Administration / exposure
- Route of administration:
- inhalation: dust
- Type of inhalation exposure:
- whole body
- Vehicle:
- other: unchanged (no vehicle)
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION- Exposure apparatus: Glass chamber- Exposure chamber volume: 160 litre- Method of holding animals in test chamber: Wire-mesh exposure cages.- Source and rate of air: rotary centrifugal air-pump located at the exhaust side of the chamber at 7.5 litres/min.- Method of conditioning air: - System of generating particulates/aerosols:Dispersing powder at a calculated rate.- Method of particle size determination: - Treatment of exhaust air:- Temperature, humidity, pressure in air chamber: TEST ATMOSPHERE- Brief description of analytical method used: - Samples taken from breathing zone: yes/noVEHICLE- Composition of vehicle (if applicable):- Concentration of test material in vehicle (if applicable):- Justification of choice of vehicle: - Lot/batch no. (if required): - Purity: TEST ATMOSPHERE (if not tabulated)- Particle size distribution:- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): CLASS METHOD (if applicable)- Rationale for the selection of the starting concentration:
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 1 h
- Concentrations:
- A total of 91.37 grams of the powders was disseminated during the 1 hour exposure period. The rate of powder dissemination was calculated to be 1.52 grams per minute. The rate of chamber airflow was 7.5 liters per minute and the chamber dust concentration was calculated to be 203.0 mg/l. The chamber atmosphere was extremely dusty.
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days - Frequency of observations and weighing: Twice daily - Necropsy of survivors performed: no- Other examinations performed: clinical signs, body weight
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 203 mg/L air
- Based on:
- other: Mortality
- Exp. duration:
- 1 h
- Mortality:
- None
- Clinical signs:
- other: The immediate response of the rats to the experimental atmosphere was an increase of activity in preening. After several minutes of exposure this activity decreased. After 30 minutes of exposure six rats exhibited salivation. By the end of the exposure
- Body weight:
- A slight body weight loss was observed in 6 rats for 1 day post-exposure.
- Gross pathology:
- None
Applicant's summary and conclusion
- Interpretation of results:
- relatively harmless
- Remarks:
- Migrated informationCriteria used for interpretation of results: EU
- Conclusions:
- Inhalation exposure of 10 rats for 1 hour to a dust atmosphere of Chlorendic Anhydride at a metered concentration of 203.0 mg / l resulted in salivation during the exposure. A slight body weight loss was observed in 6 rats for 1 day post-exposure.
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