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Diss Factsheets
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EC number: 231-198-9 | CAS number: 7446-14-2
- 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
Neurotoxicity
Administrative data
- Endpoint:
- neurotoxicity: chronic oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented publication which meets basic scientific principles
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 984
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Eight-month-old dogs maintained on a high-fat-low-calcium diet were administred a mixture of lead chloride, lead bromide and lead sulphte for prolonged periods at 4 different dose levels. The distribution of the neurological lesions of experimental lead toxicity in dogs was recorded and the associated light and electron microscopic changes were described.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Automatically generated during migration to IUCLID 6, no data available
- IUPAC Name:
- Automatically generated during migration to IUCLID 6, no data available
- Details on test material:
- The lead salt mixture consisited of lead chloride, lead bromide and lead sulphate in the proportions 1:1:2 respectively. These lead compounds in approximately similar proportions are the major by-products in the exhaust emission of internal combustion engines which utilize leaded petrol (bloom, 1979, pers. comm.). All dogs were weighed once a week and the dose of lead salt mixture was calculated.
Constituent 1
Test animals
- Species:
- dog
- Strain:
- other: Kelpie-cross
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: capsule
- Vehicle:
- other: gelatin
- Duration of treatment / exposure:
- From 14 days to 152 days
- Frequency of treatment:
- Daily
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
0 mg/kg (bw)
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
5 mg/kg (bw)
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
15 mg/kg (bw)
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
30 mg/kg (bw)
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
60 mg/kg (bw)
Basis:
nominal conc.
- No. of animals per sex per dose:
- The dogs were divided into 5 groups of 2 dogs except group 5 (60mg/kg bw) which had 3 dogs.
- Control animals:
- yes
Results and discussion
Effect levels
- Dose descriptor:
- conc. level:
- Basis for effect level:
- other: neuropathology :
- Remarks on result:
- not measured/tested
- Remarks:
- Effect level not specified
Any other information on results incl. tables
Dogs H176 and H179 first developped nervous signs on days 24 and 57 respectively, and died on days 50 and 72. Both dogs had convulsive episodes but in H179, the signs were milder than in dog H176.
The lead content of the frontal lobe of the cerebrum was high in dogs with brain lesions. Dog H180 on 30mg/kg/day of the lead salt mixture also had a high brain lead burden but neuropathological changes were not evident on examination by light microscopy.
Neither experimental nor control dogs showed macroscopic neuropathological changes. 7 of the 9 dogs in the experiment had brain lesions which were apparent under light microscope.
Applicant's summary and conclusion
- Conclusions:
- The brain lead content is not a reliable indicator of lead intoxication in dogs. Furthermore, the severity and the extent of histologically detectable brain lesions did not bear a consitent relationship to the clinical manifestations of lead neuropathy.
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