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EC number: 237-509-4 | CAS number: 13821-20-0
- 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
Toxicological Summary
- Administrative data
- Workers - Hazard via inhalation route
- Workers - Hazard via dermal route
- Workers - Hazard for the eyes
- Additional information - workers
- General Population - Hazard via inhalation route
- General Population - Hazard via dermal route
- General Population - Hazard via oral route
- General Population - Hazard for the eyes
- Additional information - General Population
Administrative data
Workers - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 37.5 mg/m³
- Most sensitive endpoint:
- acute toxicity
- Route of original study:
- By inhalation
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 22.5
- Dose descriptor starting point:
- LOAEC
- Value:
- 500 mg/m³
- Modified dose descriptor starting point:
- LOAEC
- Value:
- 844.2 mg/m³
- Explanation for the modification of the dose descriptor starting point:
Remark on the starting point :
At 500 mg/m3 one female was sacrificed on day 5 but no further clinical signs were observed during exposure. After exposure, abnormal posture, hunched posture, piloerection, dehydration, lean appearance and/or ptosis were seen among the animals. The surviving animals had recovered from the symptoms by Day 11. No abnormalities were found at macroscopic examination. Therefore, 500 mg/m3 is interpreted as a LOAEC for acute effects.
The corrected inhalatory LOAEC has been calculated considering :
- the difference of exposure conditions between experimental animals and workers (4h/d and 15min/d respectively) by applying the modified Harber's law (Cn* t = k, where ‘C’ is the concentration, ‘n’ is a regression coefficient, ‘t’ is the exposure time and ‘k’ is a constant) and a default value of n=3 for extrapolating from longer to shorter exposure durations : dose at 15min = (500^3 * (240/15))^(1/3) = 1260 mg/m3
- the difference between the standard respiratory volume and the worker respiratory volume for a light activity (i.e. 6.7 m3/person and 10m3 / person respectively) by applying a factor of 0.67
- AF for dose response relationship:
- 3
- Justification:
- The starting point for the DNEL derivation is a LOAEL.
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Allometric scaling is not applicable when setting an inhalation DNEL based on an inhalation animal study (in accordance with ECHA guidance R8)
- AF for other interspecies differences:
- 2.5
- Justification:
- For inhalation studies only a factor 2.5 is used, and no correction is made for differences in body size, because extrapolation is based on toxicological equivalence of a concentration of a chemical in the air of experimental animals and humans; animals and humans breathe at a rate depending on their caloric requirements.
- AF for intraspecies differences:
- 3
- Justification:
- An overall intraspecies factor of ≤ 3 is justified for workers when local respiratory effects by inorganic metal compounds that do not undergo metabolism are considered (Hattis et al., 1987; Hattis and Silver, 1994; Renwick and Lazarus, 1998; ECETOC 2010).
- AF for the quality of the whole database:
- 1
- Justification:
- The available information fulfil the requirement of the REACH registration.
- AF for remaining uncertainties:
- 1
- Justification:
- The global assessment factor applied is considered to be sufficiently protective as it follows the ECHA guidance R8.
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 0.11 mg/m³
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 9
- Dose descriptor:
- NOAEC
- Value:
- 1.01 mg/m³
- AF for dose response relationship:
- 1
- Justification:
- The dose descriptor is a NOAEC which is considered as an appropriate starting point.
- AF for differences in duration of exposure:
- 3
- Justification:
- Local effects such as respiratory tract irritation are more driven by the concentration of the substance rather than the duration of the exposure. Furthermore human data available on cryolite (CAS: 13775-53-6) (substance which can be choosen as an analogue) give no indication for cryolite specific chronic respiratory effects after inhalation exposure (local effects). Therefore taken into account all this information, an assessment factor of 3 for the variability of the time duration appears to be enough conservative.
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- Allometric scaling should not be applied if the effects are not dependent on metabolic rate or systemic absorption, e.g. in the case of local effects. (According to ECHA guidance R8).
- AF for other interspecies differences:
- 1
- Justification:
- For respiratory (local) toxicity effects after inhalation of particles of most metal-containing substances in the respirable range, 1-5 µm, rats seem to be more susceptible to toxicity effects than primates or humans (Oberdörster, 1995; Mauderly, 1997; ILSI, 2000; Nikula et al., 2001; Greim and Ziegler-Skylakakis, 2007).
As rats are the most sensitive animal species to the inhalation effects of inorganic particulates, further toxicodynamic adjustments are not needed. - AF for intraspecies differences:
- 3
- Justification:
- An overall intraspecies factor of ≤ 3 is justified for workers when local respiratory effects by inorganic metal compounds that do not undergo metabolism are considered (Hattis et al., 1987; Hattis and Silver, 1994; Renwick and Lazarus, 1998; ECETOC 2010).
- AF for the quality of the whole database:
- 1
- Justification:
- The available information fulfil the requirement of the REACH registration.
- AF for remaining uncertainties:
- 1
- Justification:
- The global assessment factor applied is considered to be sufficiently protective as it follows the ECHA guidance R8.
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Workers - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
Workers - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- no hazard identified
Additional information - workers
General Population - Hazard via inhalation route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- DNEL (Derived No Effect Level)
- Value:
- 7 µg/m³
- Most sensitive endpoint:
- repeated dose toxicity
DNEL related information
- DNEL derivation method:
- ECHA REACH Guidance
- Overall assessment factor (AF):
- 36
- Dose descriptor:
- other: Modified NOAEC as corrected starting point : NOAEC = 1.01 mg/m3 (results of the sub-acute inhalatin toxicity study), corrected for exposure duration in study (6 hrs/day) to default population exposure (24 hrs/day).
- Value:
- 0.25 mg/m³
- AF for dose response relationship:
- 1
- Justification:
- The dose descriptor is a NOAEC which is considered as an appropriate starting point.
- AF for differences in duration of exposure:
- 6
- Justification:
- Extrapolation from sub-acute to chronic (in accordance with ECHA guidance R8)
- AF for interspecies differences (allometric scaling):
- 1
- Justification:
- No factor for allometric scaling is needed in case of inhalation exposure.
- AF for other interspecies differences:
- 1
- Justification:
- For respiratory (local) toxicity effects after inhalation of particles of most metal-containing substances in the respirable range, 1-5 µm, rats seem to be more susceptible to toxicity effects than primates or humans (Oberdörster, 1995; Mauderly, 1997; ILSI, 2000; Nikula et al., 2001; Greim and Ziegler-Skylakakis, 2007).
As rats are the most sensitive animal species to the inhalation effects of inorganic particulates, further toxicodynamic adjustments are not needed. - AF for intraspecies differences:
- 6
- Justification:
- The critical effect is a direct local effect that is hardly if at all, mainly determined by toxicodynamics and kinetics. Absorption, distribution and elimination play no/a minor role.
An overall intraspecies factor of ≤ 3 is justified for workers when local respiratory effects by inorganic metal compounds that do not undergo metabolism are considered (Hattis et al., 1987; Hattis and Silver, 1994; Renwick and Lazarus, 1998; ECETOC 2010). Using a reduced factor of 6 is therefore justified for general population. - AF for the quality of the whole database:
- 1
- Justification:
- The available information fulfil the requirement of the REACH registration.
- AF for remaining uncertainties:
- 1
- Justification:
- The global assessment factor applied is considered to be sufficiently protective as it follows the ECHA guidance R8.
Acute/short term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
DNEL related information
General Population - Hazard via dermal route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
DNEL related information
Local effects
Long term exposure
- Hazard assessment conclusion:
- no hazard identified
Acute/short term exposure
- Hazard assessment conclusion:
- no hazard identified
General Population - Hazard via oral route
Systemic effects
Long term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
DNEL related information
- Explanation for the modification of the dose descriptor starting point:
The oral route is not relevant for the exposure of lithium cryolite.
Acute/short term exposure
- Hazard assessment conclusion:
- low hazard (no threshold derived)
DNEL related information
General Population - Hazard for the eyes
Local effects
- Hazard assessment conclusion:
- low hazard (no threshold derived)
Additional information - General Population
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.
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