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Diss Factsheets
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EC number: 203-016-8 | CAS number: 102-24-9
- 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: Non-GLP study, no guideline followed; not single exposure but 9
Data source
Reference
- Reference Type:
- publication
- Title:
- The subacute inhalation toxicity of 109 industrial chemicals
- Author:
- Gage
- Year:
- 1 970
- Bibliographic source:
- Brlt . J. industr . Med., 1970, 27, 1-1 8
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Rats were exposed to the test substance for 6h/d nine times; in this study the effect of several chemicals following inhalation was tested
- GLP compliance:
- no
- Test type:
- other: repeated inhalation
Test material
- Reference substance name:
- Triboron trimethyl hexaoxide
- EC Number:
- 203-016-8
- EC Name:
- Triboron trimethyl hexaoxide
- Cas Number:
- 102-24-9
- Molecular formula:
- C3H9B3O6
- IUPAC Name:
- trimethoxy-1,3,5,2,4,6-trioxatriborinane
- Details on test material:
- The samples submitted by ICI Divisions were prepared in either the Research Department or an experimental plant, or were taken from full-scale production
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Alderley Park specific-pathogen-free rats
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- No details in environmental condictions given
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Details on inhalation exposure:
- Atmospheres were continuously generated and passed through the exposure chamber. The air used fot the atmospheres was filtered, dried to a
relative humidity of less than 10%, and supplied at a line pressure of 1 atm. A nearly saturated vapour obtained by passing air through a liquid contained in a bubbler with a sintered glass air-distributor disc . The volume of the liquid was usually 10-20 ml and, if the size of the sample available permitted, it was replaced daily . Unless otherwise stated, the bubbler was maintained in a water-bath at room temperature, about 20°C.
The nearly saturated concentration was estimated by weighing the sample before and after the day's run, and relating the weight loss to the volume of air passing . This concentration, expressed in milligrammes per litre, was converted to parts per million on the assumption that the sample was pure . - Analytical verification of test atmosphere concentrations:
- not specified
- Duration of exposure:
- 6 h
- Remarks on duration:
- 9 exposures
- Concentrations:
- Saturated atmosphere
- No. of animals per sex per dose:
- 3 M/ 4F
- Details on study design:
- Rats were weighed each morning, and their conditions and behaviour were recorded throughout the exposure period . Urine was collected overnight after the last exposure day for biochemical tests . The animals were left overnight with food and drink . On the following day the rats were anaesthetized with halothane and partially exsanguinated by heart puncture for haematological tests . After a gross examination of the organs, the lungs were inflated with formol-saline and immersed in the same fixative . The following organs were also taken for microscopical examination after fixation
in formol-corrosive : lungs, liver, kidneys, spleen, and adrenals ; and occasionally heart, jejunum, ileum, and thymus.
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- > 3 mg/L air
- Mortality:
- no mortalities described
- Clinical signs:
- other: slight lethargy
- Body weight:
- no data
- Gross pathology:
- Organs normal
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.