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EC number: 215-183-4 | CAS number: 1310-65-2
- 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

Repeated dose toxicity: oral
Administrative data
- Endpoint:
- chronic toxicity: oral
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Justification for type of information:
- HYPOTHESIS FOR THE ANALOGUE APPROACH
Lithium hydroxide completely dissociates in water forming lithium cation and the corresponding hydroxide anion. Thus, lithium salts with different anion moieties and hydroxide compounds were found to be suitable candidates for read-across. (Eco)toxicological properties were extrapolated to different endpoints by using the lowest effect concentration.
For further information, please refer to the read-across justification in chapter 13.
Cross-reference
- Reason / purpose for cross-reference:
- read-across source
Reference
- Endpoint:
- chronic toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 1958, 1995, 2002
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: publication
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 452 (Chronic Toxicity Studies)
- Principles of method if other than guideline:
- No data
- GLP compliance:
- not specified
- Remarks:
- study was published in 1958
- Species:
- rat
- Strain:
- other: albino Wistar
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight:
females: 0.14 kg - 0.18 kg
males: 0.2 - 0.27 kg - Route of administration:
- oral: drinking water
- Vehicle:
- water
- Details on oral exposure:
- 10-12 g/0.1 kg/bw /day
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 84.8 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: Worst case NOAEL Lithium chloride intake
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 13.9 mg/kg bw/day (nominal)
- Based on:
- other: Lithium content of test material
- Sex:
- male/female
- Basis for effect level:
- other: Worst case Lithium intake
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 2 other: mmol/kg bw/day
- Based on:
- other: Lithium content of test material
- Sex:
- male/female
- Basis for effect level:
- other: Worst case Lithium intake
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 138.07 mg/kg bw/day (nominal)
- Based on:
- other: Based on lithium content of test material and calculated for LiNO3
- Sex:
- male/female
- Basis for effect level:
- other: Worst case Lithium intake
- Critical effects observed:
- not specified
- Conclusions:
- In a 2-year study in rats ingesting drinking water containing lithium chloride in a concentration of 20 mmol no effects on health or behaviour were found, except slight, transitory initial disturbances. When a concentration of 50 mmol LiCl/L was administered, food and water intake was decreased within a few days, and the rats became progressively drowsy and asocial on the 3rd to 5th day. Their gait was staggering, and they had a fine muscular tremor. Simultaneously their weight began to drop. The deterioration progressed to stupor and death within 2-3 weeks.
Plasma levels at dose level 20 mmol/L: 1.5 - 2 mmol
Lithium Plasma levels at dose level 50 mmol/L: 3 (behavioural changes) - 8 (death) mmol Lithium.
The Lithium concentration of 20 mmol/L used in this chronic drinking water study, is comparable to the highest doses given temporarily to hospitalised patients (plasma lithium level about 2 mmol/L).
The daily water intake was 0.010 - 0.012 kg / 0.1 kg bw.
For worst case considerations, the daily Lithium intake in rat is 2.0 mmol/kg bw/day which is equivalent to 13.881 Lithium mg/kg bw/ day.
Thus, a worst case NO(A)EL of 13.9 mg Lithium/kg bw/ day can be derived. - Executive summary:
In a 2-year study in rats ingesting drinking water containing lithium chloride in a concentration of 20 mmol no effects on health or behaviour were found, except slight, transitory initial disturbances. When a concentration of 50 mmol LiCl/L was administered, food and water intake was decreased within a few days, and the rats became progressively drowsy and asocial on the 3rd to 5th day. Their gait was staggering, and they had a fine muscular tremor. Simultaneously their weight began to drop. The deterioration progressed to stupor and death within 2-3 weeks. Plasma levels at dose level 20 mmol/L: 1.5 - 2 mmol lithium plasma levels at dose level 50 mmol/L: 3 (behavioural changes) - 8 (death) mmol lithium. Based on the result, a worst case NOAEL of 2.0 mmol lithium /kg bw/day, corresponding to 13.9 mg lithium /kg bw/ day was derived and calculated to be 138 mg/kg bw/day for lithium nitrate.
Dose level 20 mmol lithium chloride / L:
This dose was just subtoxic; apart from slight initial disturbances, it caused no effects on health or behaviour in the adult animals over a period of up to two years.
Plasma levels: 1.5 - 2 mmol lithium
Dose level 50 mmol lithium chloride / L:
The animals appeared to be unchanged in aspect and behaviour for 3 to 5 days. Then they became progressively drowsy and asocial. They were difficult to rouse; when roused, their gait was staggering and hesitant and they rested again as soon as possible. When resting they showed fine muscular tremor and trembling; usually they sat for long periods by themselves anywhere in the box. A few days later they became unresponsive and were stuporous, with dull eyes and slightly erected, untidy and unkempt fur. They were visibly ill and emaciated. Death occurred within 2 to 3 weeks.
Plasma levels: 3 (behavioural changes) - 8 (death) mmol lithium
Data source
Materials and methods
Test material
- Reference substance name:
- Lithium hydroxide
- EC Number:
- 215-183-4
- EC Name:
- Lithium hydroxide
- Cas Number:
- 1310-65-2
- Molecular formula:
- HLiO
- IUPAC Name:
- lithium hydroxide
- Test material form:
- solid
Constituent 1
Results and discussion
Effect levels
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 47.97 mg/kg bw/day (nominal)
- Based on:
- other: recalculated for LiOH
- Sex:
- male/female
- Remarks on result:
- other: based on LiCl (Trautner, 1958)
Target system / organ toxicity
- Key result
- Critical effects observed:
- no
Applicant's summary and conclusion
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