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EC number: 231-195-2 | CAS number: 7446-09-5
- 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
Repeated dose toxicity: inhalation
Administrative data
- Endpoint:
- sub-chronic toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Entry adopted from the OECD SIAR on sulfur dioxide without modification.Concerning the investigated endpoints the study is comparable to a guideline study: well documented, adequate number of exposed animals, appropriate exposure and post-exposure periods; specific investigation of body and lung weight, histopathology of lung and nose and particle clearance at a single low concentration; study acceptable for assessment.
Data source
Reference
- Reference Type:
- publication
- Title:
- Effects of repeated inhalation exposures to 1-nitropyrene, benzo[a]pyrene, Ga2O3, particles and SO2 alone and in combinations on particle clearance, bronchoalveolar lavage fluid composition, and histopathology.
- Author:
- Wolff, R.K. et al.
- Year:
- 1 989
- Bibliographic source:
- J Toxicol Environ Health 27: 123 - 138.
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Concerning the investigated endpoints the study is comparable to a guideline study: well documented, adequate number of exposed animals, appropriate exposure and post-exposure periods; specific investigation of body and lung weight, histopathology of lung and nose and particle clearance at a single low concentration; study acceptable for assessment.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Sulphur dioxide
- EC Number:
- 231-195-2
- EC Name:
- Sulphur dioxide
- Cas Number:
- 7446-09-5
- Molecular formula:
- SO2
- IUPAC Name:
- Sulphur dioxide generated from sulphur by combustion
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): sulfur dioxide
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: from the Institute's breeding colony
- Age at study initiation: 7-8 weeks
- Housing: Rats were housed and maintained in two types of facilities. Before and after inhalation exposure periods they were hosed one or two per cage in polycarbonate cages with hardwood chip bedding and filter caps.
- Diet: ad libitum, Lab Blox, Allied Mills, Chicago
- Water: ad libitum
- Acclimation period: 1-2 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-22
- Humidity (%): 30-50
- Photoperiod: 12 hours dark/light cycle
No further details are given.
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- nose only
- Vehicle:
- other: air
- Remarks on MMAD:
- MMAD / GSD: no data
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Method of holding animals in test chamber: For the conduct of all inhalation exposures, rats were maintained in carcinogen exposure units, which each contained both wire mesh caging for housing up to 80 rats and an 80-port nose-only exposure chamber. For the majority of the time, rats were resident in the wire mesh cages with food available ad libitum. Water was also available, ad libitum, from automatic water valves.
- System of generating particulates/aerosols: SO2 was generated by dilution in air of 1% SO2 delivered from a compressed gas cylinder and metered by a mass flow controller.
- Method of particle size determination: Particle exposure concentrations were detremined by weighing filter samples taken throughout each 2-hour exposure.
No further details are given. - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Concentrations were monitored continuously with a Beckman SO2 analyser.
- Duration of treatment / exposure:
- 4-week exposure
- Frequency of treatment:
- 2 hours/day, 5 days/week
Doses / concentrations
- Dose / conc.:
- 5.2 ppm (analytical)
- Remarks:
- SD: ± 0.6 ppm
- No. of animals per sex per dose:
- Groups of 3 male and 3 female rats were exposed.
- Control animals:
- yes
- Details on study design:
- Groups of rats were exposed to atmospheres of pure 1-nitropyrene (NP) aerosol (7.5 mg/m^3) and to these same compounds adsorbed to Ga2O3 particles (27 mg/m^3) both with and without co-exposure to 5 ppm SO2. Rats were also exposed to SO2 alone.
There were 80 rats per exposure group (equal numbers of males and females). The SO2 concentration was set at 5 ppm. This is the short-term industrial threshold limit value (American Conference of Governmental Industrial Hygienists, 1987). - Positive control:
- no
Examinations
- Observations and examinations performed and frequency:
- CAGE SIDE OBSERVATIONS: No data
DETAILED CLINICAL OBSERVATIONS: No data
BODY WEIGHT: Yes
- Time schedule for examinations:
FOOD CONSUMPTION: No data
FOOD EFFICIENCY: No data
WATER CONSUMPTION: No data
OPHTHALMOSCOPIC EXAMINATION: No data
HAEMATOLOGY: No data
CLINICAL CHEMISTRY: No data
URINALYSIS: No data
NEUROBEHAVIOURAL EXAMINATION: No data
OTHER: Lung weight - Sacrifice and pathology:
- HISTOPATHOLOGY: Yes
Groups of rats were sacrificed for histopathologic evaluations 1 day, 2 weeks, 2 months, 6 months and 12 months after the exposure period by exsanguination while under halothane anesthesia. The right lung was examined and then taken for lung analysis of the gallium oxide burden. The left lung was intratracheally perfused to normal inflation with fixative. Nasal sections were examined because they were also an initial deposition site. Trimmed tissues were embedded in paraffin, sectioned at 5 µm, and stained with haematoxylin and eosin. Slides were examined by light microscopy. Morphologic changes were identified and graded for their severity in each rat.
GROSS PATHOLOGY: No data - Other examinations:
- no data
- Statistics:
- Analysis of variance using repeated measures and fractional factorial analysis was used to determine if there were significant effects of grouping factors of exposure to SO2 on body weight, lung weight, lung burdens or clearance of radiolabelled tracer particles..
The criterion for statistical significance was p<0.05.
Results and discussion
Results of examinations
- Clinical signs:
- not specified
- Mortality:
- not specified
- Body weight and weight changes:
- effects observed, treatment-related
- Food consumption and compound intake (if feeding study):
- not specified
- Food efficiency:
- not specified
- Water consumption and compound intake (if drinking water study):
- not specified
- Ophthalmological findings:
- not specified
- Haematological findings:
- not specified
- Clinical biochemistry findings:
- not specified
- Urinalysis findings:
- not specified
- Behaviour (functional findings):
- not specified
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Gross pathological findings:
- not specified
- Histopathological findings: non-neoplastic:
- no effects observed
- Histopathological findings: neoplastic:
- not specified
- Details on results:
- BODY WEIGHT AND WEIGHT GAIN
There was no significant difference in body weight among the groups either before or at any time after the cessation of the 4-week exposure (data not shown).
ORGAN WEIGHTS
Lung weights of exposed rats were similar to those of controls 12 months after exposure.
HISTOPATHOLOGY:
There were no significant lung lesions in any of the experimental groups at any time after exposure to SO2. No significant lesions were found in the nasal cavities of rats in any of the experimental groups.
No further details are given.
Effect levels
- Dose descriptor:
- NOAEL
- Effect level:
- 5 ppm
- Sex:
- male/female
- Basis for effect level:
- other: overall effects body weight; organ weights: liver weight; histopathology of lung and nose tissue (examination by light microscopy);
Target system / organ toxicity
- Critical effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- Subacute exposure of rats (4 weeks, 2 hours/day, 5 days/week) to 5 ppm sulfur dioxide by nose-only exposure was without any effect on body or lung weights, histopathology of lung and nose tissue (examination by light microscopy), or particle clearance.
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