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EC number: 204-468-9 | CAS number: 121-43-7
- 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

Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Study period:
- 01/10/2009 to 07/12/2009
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: The protocol was designed based on the ASTM E981-04 (2004) method, Standard Test Method for Estimating Sensory Irritancy of Airborne Chemicals (American Society for Testing and Materials, published May, 2004).
- Deviations:
- not specified
- Principles of method if other than guideline:
- The objective of this study was to evaluate the potential for boric acid and sodium tetraborate pentahydrate to produce depression of respiratory rate resulting from airway sensory irritation when administered to male Swiss-Webster mice by whole-head (head-only) inhalation exposure. Respiratory depression may result from upper airway sensory irritation and/or pulmonary irritation.
The protocol was designed based on the ASTM E981-04 (2004) method, Standard Test Method for Estimating Sensory Irritancy of Airborne Chemicals (American Society for Testing and Materials, published May, 2004).
The respiratory depression of boric acid and sodium tetraborate pentahydrate, was evaluated in 30-minute, single-exposure study in Swiss-Webster Crl:CFW® (SW)BR mice. Boric acid was administered to several exposure levels of 4 male mice via head-only inhalation exposure as a dust aerosol at geometrically spaced concentrations. - GLP compliance:
- yes
- Type of method:
- in vivo
- Endpoint addressed:
- respiratory irritation
Test material
- Reference substance name:
- Boric acid; Sodium tetraborate pentahydrate
- IUPAC Name:
- Boric acid; Sodium tetraborate pentahydrate
- Details on test material:
- - Name of test material: Boric acid; Sodium tetraborate pentahydrate
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- Swiss Webster
- Sex:
- male
Administration / exposure
- Route of administration:
- inhalation: dust
- Vehicle:
- not specified
- No. of animals per sex per dose:
- 4 males.
Results and discussion
- Details on results:
- It was not possible to achieve an RD50 for boric acid or sodium tetraborate pentahydrate based on the results in the mouse sensory irritation model.
Respiratory depression expressed as group mean percent decrease from baseline respiratory rate was as follows for sodium tetraborate pentahydrate: 14%, 11%, 17%, 17%, 19%, 25%, 28%, and 33% for aerosol concentrations of 231, 186, 394, 681, 886, 798, 1442, and 1704 mg/m3, respectively. The highest concentration of sodium borate that was achievable with acceptable control of the aerosol concentration was 1735 mg/m3 with a %RD of 41 %.
Respiratory depression expressed as group mean percent decrease from baseline respiratory rate was as follows for boric acid: 9%, 21%, 15%, 14%, 18%, 8%, 15%, 15%, 19%, 19%, 21%,and 17% for aerosol concentrations of 221, 381, 436, 464, 528, 709, 650, 613, 762, 759, 1018, and 1174 mg/m3, respectively. The highest concentration of boric acid that was achievable with acceptable control of the aerosol concentration was 1096 mg/m3 with a %RD of 19 %.
Based on these results, the RD50 is > 1096 mg/m3 for boric acid, and > 1735 mg/m3 for sodium tetraborate pentahydrate.
Applicant's summary and conclusion
- Conclusions:
- The objective of this study was to evaluate the potential for boric acid and sodium tetraborate pentahydrate to produce depression of respiratory rate resulting from airway sensory irritation when administered to male Swiss-Webster mice by whole-head (head-only) inhalation exposure. Respiratory depression may result from upper airway sensory irritation and/or pulmonary irritation.
The protocol was designed based on the ASTM E981-04 (2004) method, Standard Test Method for Estimating Sensory Irritancy of Airborne Chemicals (American Society for Testing and Materials, published May, 2004).
The respiratory depression of boric acid and sodium tetraborate pentahydrate, was evaluated in 30-minute, single-exposure study in Swiss-Webster Crl:CFW® (SW)BR mice. Boric acid was administered to several exposure levels of 4 male mice via head-only inhalation exposure as a dust aerosol at geometrically spaced concentrations.
It was not possible to achieve an RD50 for boric acid or sodium tetraborate pentahydrate based on the results in the mouse sensory irritation model.
The highest concentration of sodium borate that was achievable with acceptable control of the aerosol concentration was 1735 mg/m3 with a %RD of 41%.
The highest concentration of boric acid that was achievable with acceptable control of the aerosol concentration was 1097 mg/m3 with a %RD of 19%.
Based on these results, the RD50 is > 1097 mg/m3 for boric acid, and > 1735 mg/m3 for sodium tetraborate pentahydrate.
The RD10 values calculated for both substances was 189 mg/m3.
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.

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