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Diss Factsheets
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EC number: 233-797-0 | CAS number: 10361-82-7
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Guidelines of the Department of Transportation (D.O.T.), Code of Federal Regulations, Title 49, Part 173
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Lanthanum chloride trihydrate
- IUPAC Name:
- Lanthanum chloride trihydrate
- Details on test material:
- - Name of test material (as cited in study report): Rare Earth Solution Code #1455
- Molecular formula (if other than submission substance): LaCl3*3(H2O)
- Physical state: amber liquid
- Concentration of solution: 100%
- Analytical purity: no data
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Taconic Farms Inc.
- Weight at study initiation: 100 - 150 g
- Fasting period before study: overnight
- Housing: 5 per wire mesh suspended cage
- Diet (Purina Laboratory Chow) and water ad libitum
- Acclimation period: 7 d
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Details on oral exposure:
- MAXIMUM DOSE VOLUME APPLIED: 0.9 mL
RANGE FINDING STUDY
- Concentrations tested: 3980, 6320, and 10000 mg/kg
- 2 animals per concentration
- result: No. dead/No. dosed: 10000 mg/kg: 2/2; 6320 mg/kg: 2/2; 3980 mg/kg: 1/2 - Doses:
- 2820, 3550 and 4470 mg/kg bw
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 48 hours
- Frequency of observations and weighing: clinical signs were noted immediately after dosing and at 4, 24, and 48 hours; body weights were recorded at dosing and at 48 hours for the survivors.
- Animals found dead or terminated after 48 hours were subjected to a macroscopic examination of the viscera. - Statistics:
- LD50 was calculated according to the method of: Litchfield and Wilcoxon, Pharmacol. and Exp. Ther. 96(99): 1499
Results and discussion
Effect levelsopen allclose all
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 3 200 mg/kg bw
- 95% CL:
- > 2 883 - < 3 552
- Remarks on result:
- other: 48 hours; Test substance: Rare Earth Solution Code #1455
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 2 621 mg/kg bw
- 95% CL:
- > 2 361 - < 2 909
- Remarks on result:
- other: 48 hours; Test substance: Lanthanum chloride, anhydrous
- Mortality:
- 4470 mg/kg: 8 out of 10 died within 24 h, 1 out of 10 died within 48 h
3550 mg/kg: 6 out of 10 died within 24 h, 2 out of 10 died within 48 h
2820 mg/kg: 2 out of 10 died within 24 h, no further deaths within 48 h - Clinical signs:
- other: 4470 mg/kg: all animals were prostate after dosing and at 4 h. 3550 mg/kg: all animals were lethargic after dosing and didn´t recover until they died or were sacrificed. 2820 mg/kg: all animals were lethargic after dosing and at 4 h; after 24 h 2 animals
- Gross pathology:
- 4470 mg/kg: dead animals: test solution in stomach and intestine; sacrificed animal: no gross pathology - Diarrhea
3550 mg/kg: dead animals: test solution in stomach and intestine; sacrificed animals: no gross pathology - Diarrhea
2820 mg/kg: dead animals: test solution in stomach and intestine; sacrificed animals: no gross pathology (3 animals) or distended stomachs (5 animals)
No gross pathology was performed with surviving animals.
Any other information on results incl. tables
Mortality:
Concentration (mg/kg) |
Mortality: No. Dead / No. Dosed |
||
4 h |
24 h |
48 h |
|
males |
|
|
|
4480 |
0/5 |
4/5 |
1/5 |
3550 |
0/5 |
4/5 |
0/5 |
2820 |
0/5 |
2/5 |
0/5 |
females |
|
|
|
4480 |
0/5 |
4/5 |
0/5 |
3550 |
0/5 |
2/5 |
2/5 |
2820 |
0/5 |
0/5 |
0/5 |
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.