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EC number: - | CAS number: -
- 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
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- Endpoint summary
- Stability
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- 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
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- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
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- Genetic toxicity
- Carcinogenicity
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- Specific investigations
- Exposure related observations in humans
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- Additional toxicological data

Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 017
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.1100 (Acute Oral Toxicity)
- GLP compliance:
- yes (incl. QA statement)
- Test type:
- acute toxic class method
Test material
- Reference substance name:
- Dilithium tetraborate
- EC Number:
- 234-514-3
- EC Name:
- Dilithium tetraborate
- Cas Number:
- 12007-60-2
- Molecular formula:
- B4Li2O7
- IUPAC Name:
- dilithium tetraborate
- Test material form:
- solid: bulk
Constituent 1
- Specific details on test material used for the study:
- Test item storage: At room temperature
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Deutschland, Sulzfeld, Germany
- Sex: 9 Females (nulliparous and non-pregnant). Each dose group consisted of 3 animals.
- Age at study initiation: Young adult animals (approximately 10-11 weeks old) were selected.
- Weight at study initiation: 165 to 200 g.
- Housing: polycarbonate cages (Makrolon MIV type; height 18 cm.) containing sterilized sawdust as bedding material (Lignocel S 8-15, JRS - J.Rettenmaier & Söhne GmbH + CO. KG, Rosenberg, Germany) equipped with water bottles.
- Diet: Pelleted rodent diet (SM R/M-Z from SSNIFF® Spezialdiäten GmbH, Soest, Germany) was provided ad libitum
- Water: Municipal tap-water was freely available
- Acclimation period: At least 5 days before dosing.
- Animals were deprived of food overnight (for a maximum of 20 hours) prior to dosing and until 3-4 hours after administration of the test item.
ENVIRONMENTAL CONDITIONS
- 18 to 24°C with a relative target humidity of 40 to 70%
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- other: medicinal white oil
- Details on oral exposure:
- VEHICLE
- Identification: MOL WO M46 medicinal white oil
- Justification for choice of vehicle: The vehicle was selected based on information provided by the Sponsor
- Lot/batch no. (if required): 208885/A
- Specific gravity: 0.833-0.893 g/cm3 (at 15°C)
A dose volume of 10 mL/kg body weight was used for each dose.
The oral route was selected as it is a possible route of human exposure during manufacture, handling or use of the test item.
The dose levels were based on the OECD test guidelines and were selected from the series 5 (lowest dose level), 50, 300 and 2000 (highest dose level) mg/kg body weight. - Doses:
- The first group was treated at a dose level of 2000 mg/kg. Based on the results, two additional groups were dosed at 300 mg/kg.
- No. of animals per sex per dose:
- 3 Females per dose group.
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Throughout the study, animals were observed for general health/mortality and moribundity twice daily, in the morning and at the end of the working day. Postdoes observations were performed at periodic intervals on the day of dosing (at least three times) and once daily thereafter. All the animals were examined for reaction to dosing and the onset,intensity and duration of these signs were recorded.
- All animals assigned to the study were subjected to necropsy and descriptions of all internal macroscopic abnormalities were recorded.
- The body weights of the animals were recorded individually on Day 1 (predose), 8 and 15.
Results and discussion
- Preliminary study:
- Not applicable
Effect levels
- Key result
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- 500 mg/kg bw
- Based on:
- test mat.
- Mortality:
- At 2000 mg/kg, all animals were found dead on Day 2. At 300 mg/kg, no mortality occurred.
- Clinical signs:
- other: Hunched posture, uncoordinated movements, piloerection and ptosis were noted for all animals on Day 1 at 2000 mg/kg. At 300 mg/kg, hunched posture, uncoordinated movements and piloerection were noted for all animals between Days 1 and 2.
- Gross pathology:
- Abnormalities of the stomach (gelatinous contents and/or dark red/discoloured/thickened glandular mucosa) were found in the animals that died during the study, at macroscopic post mortem examination. Macroscopic post mortem examination of the surviving animals at termination did not reveal any abnormalities.
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- The oral LD50 value of dilithium tetraborate in Wistar rats was established to be within the range of 300-2000 mg/kg body weight. According to the OECD 423 test guideline, the LD50 cut-off value was considered to be 500 mg/kg body weight.
- Executive summary:
The potential toxicity of dilithium tetraborate was investigated by administration of a single dose of the test substance by oral gavage to female rats according to OECD 423. Initially, Dilithium tetraborate was administered by oral gavage to three female Wistar rats at 2000 mg/kg body weight. At 2000 mg/kg, all animals were found dead on Day 2. Two additional groups were dosed at 300 mg/kg body weight. At this dose level, no mortalities were observed but effects including hunched posture, uncoordinated movements and piloerection were noted for all animals between Days 1 and 2. For both dose levels, the body weight gain of the surviving animals was shown to be normal over the study period.
The oral LD50 value of dilithium tetraborate in Wistar rats was therefore established to be within the range of 300-2000 mg/kg body weight. According to the OECD 423 test guideline, the LD50 cut-off value was considered to be 500 mg/kg body weight.
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