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EC number: 231-569-5 | CAS number: 7637-07-2
- 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
The LC50/4hours is 1210 mg/m3 in rats (Rusch, 1986). Animals mainly exhibited typical clinical signs of respiratory distress.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- LD50
- Value:
- 326 mg/kg bw
- Quality of whole database:
- according to a BASF study (1978) for the classification of Boron trifluoride dihydrate.
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- LC50
- Value:
- 1 210 mg/m³ air
Additional information
The LC50/4 hours was calculated to be around 1210 mg/m3 when rats were whole body exposed by inhalation to aerosols of BF3 dihydrate (Rush, 1986). The animals exhibited typical signs of respiratory distress including gasping, lacrymation, nasal and oral discharge. Quite similar range of LC50 were reported in rats : LC50/4hours of 1180 mg/m3 (Kasparov, 1972) and LC50/1 hour of 820.4 -1313 mg/m3, indicative that the substance has a high potential of acute toxicity by inhalation.
The NOAEL for respiratory irritation following a single exposure of 4 hours to low dose levels was estimated around 24.6 mg/m3 (Rush, 2008).
Justification for classification or non-classification
According to EU directive 67/548/EEC, the substance should be classified as toxic by inhalation instead of very toxic by inhalation. According to EU Regulation (EC) N0. 1272/2008 (CLP) BF3 should be classified acute toxicity category 3 regarding the LC50/4 hours of about 1000 mg/m3 for exposure to aerosols of BF3. Nevertheless, the current classification (acute toxicity category 2) is not challenged.
According to a BASF study dated 1978, a classification acute toxicity category 4 H302, EU Regulation (EC) N0. 1272/2008 (CLP) is applied for the oral route for the boron trifluoride dihydrate form.
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