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EC number: 700-066-7 | CAS number: 1472633-72-9
- 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
Endpoint summary
Administrative data
Description of key information
A 90 day oral feed study gave a NOAEL of 230 mg/kg bw/day Disodium tetraborate decahydrate, equivalent to 26 mg B/kg bw/day.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Link to relevant study records
- Endpoint:
- sub-chronic toxicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- No data
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Meets generally accepted scientific standards with acceptable restrictions.
- Qualifier:
- according to guideline
- Guideline:
- other: No data
- Deviations:
- not specified
- Principles of method if other than guideline:
- Male and female Sprague-Dawley rats were exposed daily to the test substance in the diet, which was available ad libitum. A concurrent no treatment control group was included.
- GLP compliance:
- no
- Remarks:
- Study pre-dates GLP
- Limit test:
- no
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Route of administration:
- oral: feed
- Vehicle:
- not specified
- Analytical verification of doses or concentrations:
- not specified
- Duration of treatment / exposure:
- 90 Days
- Frequency of treatment:
- Daily; food ad lib
- Remarks:
- Doses / Concentrations:
0, 7.8, 23, 78 and 230 mg/kg bw/d, equivalent to 0, 17.5, 52.5, 175 and 525 ppm boron; equivalent boron 0, 0.88, 2.6, 8.8, and 26 mg B/kg bw/d.
Basis:
actual ingested - No. of animals per sex per dose:
- 10/sex/group
- Control animals:
- yes, concurrent no treatment
- Details on results:
- No adverse effect were observed at any dose tested.
- Dose descriptor:
- NOAEL
- Effect level:
- 230 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: No adverse effects were observed at any dose tested.
- Dose descriptor:
- NOAEL
- Effect level:
- 26 mg/kg bw/day (nominal)
- Based on:
- element
- Sex:
- male/female
- Critical effects observed:
- not specified
- Conclusions:
- No adverse effects were observed at any dose tested.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 26 mg/kg bw/day
- Study duration:
- subchronic
- Species:
- rat
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
The reference substance (BAGE) hydrolyses within less than an hour to its hydrolysis products: Boric acid and glycerol. Therefore, conducting repeat dose toxicity studies on the reference substance will give a result representative of the hydrolysis products mentioned above.
Boric acid is considered to be the hydrolysis product of main concern, due to its known toxic effects. An assessment of the repeat dose toxicity of boric acid has therefore been made based on available repeat dose study data conducted on Disodium tetraborate decahydrate.
Exposures to borates are often expressed in terms of boron (B) equivalents based on the fraction of boron in the source substance on a molecular weight basis. Only boric acid and the borate anion are present at physiologically relevant concentrations. Read- across between the different boron compounds can be done on the basis of boron (B) equivalents. It is therefore considered that the results of the study conducted on Disodium tetraborate decahydrate (expressed in boron equivalents) are appropriate in the assessment of boric acid.
Weir RJ (1963):
A 90 Day dietary administration study in rats was conducted on Disodium tetraborate decahydrate.
Male and female Sprague-Dawley rats were exposed daily to the test substance in the diet, which was available ad libitum. A concurrent no treatment control group was included.
The test concentrations were: 0, 7.8, 23, 78 and 230 mg/kg bw/d, equivalent to 0, 17.5, 52.5, 175 and 525 ppm boron; equivalent boron 0, 0.88, 2.6, 8.8, and 26 mg B/kg bw/d.
No adverse effects were observed at any dose level tested.
Therefore the NOAEL was 230 mg/kg bw/d, equivalent boron 26 mg B/kg bw/d.
Glycerol
Glycerol is the other hydrolysis product of BAGE. It is not classified for human health according to CLP or DSD and is essentially non-toxic. Further evaluation of the repeat dose toxicity of glycerol has not been assessed.
Refer to section 13, Toxicological expert report, for further details of the evalaution of the hydrolysis of BAGE and its consequences for toxicity testing.
Justification for classification or non-classification
Boric acid is not classified for repeat dose toxicity (STOT-RE).
The available 90 day oral feed study showed no adverse effects at any dose level tested (highest test concentration 230 mg/kg bw/d, equivalent to 26 mg B/kg bw/d).
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