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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
Direct observations: clinical cases, poisoning incidents and other
Administrative data
- Endpoint:
- direct observations: clinical cases, poisoning incidents and other
- Type of information:
- other: human case
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Entry adopted from the OECD SIAR on sulfur dioxide without modification.well ducumented study
Data source
Reference
- Reference Type:
- publication
- Title:
- Effects of inhalation of sulphur dioxide by man
- Author:
- Amdur; M.O.; et al.
- Year:
- 1 953
- Bibliographic source:
- The Lancet, Oct. 10, 1953: 758
Materials and methods
- Study type:
- study with volunteers
- Endpoint addressed:
- acute toxicity: inhalation
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Study reports exposure- related observations in human: Respiratory response of man to low concentrations of sulfur dioxide.
- GLP compliance:
- no
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
- Details on test material:
- - Name of test material (as cited in study report): sulfur dioxide
No further details are given.
Constituent 1
Method
- Type of population:
- general
- occupational
- Subjects:
- no details given
- Ethical approval:
- not specified
- Route of exposure:
- inhalation
- Reason of exposure:
- intentional
- Exposure assessment:
- measured
- Details on exposure:
- Concentrations of sulfur dioxide were established in a 2c.ft. "Lucite" chamber by metering in diluted SO2 (1% in air) from a steel cylinder. The SO2 joined the main air stream before entering the chamber. The concentrations of SO2 in the chamber were measured.
The subjects of the experiment were at rest and breathed through a face-mask. - Examinations:
- The volume of expired air was measured in a spirometer, which was read every minute. The respiratory rate and pattern were obtained with a pneumotachograph, a device for instantaneous recording of air-flow during breathing. From direct tracing the whole breathing pattern, inspiratory and expiratory flow-rates, and other breathing characteristics can be obtained.
- Medical treatment:
- no medication
Results and discussion
- Clinical signs:
- At 5 ppm most people complained of a slight feeling of dryness in the throat and upper respiratory passages, but they could not actually "smell" SO2. One person found at 5 ppm so objectionable that the exposure was stopped after 5 minutes, whereas other barely noticed it. People exposed to 6-8 ppm definitely detected SO2 in the air but said they became accustomed to it as the exposure continued.
- Results of examinations:
- 14 normal people exposed to SO2 1-8 ppm showed changes in respiration and pulse-rate. Tidal volume decreased, respiratory rate increased, minute volume remained unchanged, and pulse rate increased.
- Effectivity of medical treatment:
- no medication
Applicant's summary and conclusion
- Conclusions:
- At 5 ppm most people complained of a slight feeling of dryness in the throat and upper respiratory passages, but they could not actually "smell" SO2. One person found at 5 ppm so objectionable that the exposure was stopped after 5 minutes, whereas other barely noticed it. People exposed to 6-8 ppm definitely detected SO2 in the air but said they became accustomed to it as the exposure continued.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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