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Diss Factsheets
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EC number: 215-687-4 | CAS number: 1344-09-8
- 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

Toxicity to terrestrial arthropods
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to terrestrial arthropods: short-term
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 June - 09 August 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline study
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 850.3020 (Honey Bee Acute Contact Toxicity)
- Deviations:
- no
- GLP compliance:
- yes
- Remarks:
- no attest of authority; California Agricultural Research Inc., Kerman, CA, USA
- Application method:
- contact
- Analytical monitoring:
- no
- Vehicle:
- yes
- Details on preparation and application of test substrate:
- - Method of test material application: single topical dose
- Body part: thorax or abdomen
- Volume of test solution applied: 5 µL
- Controls: untreated and with 5 µL sterile water
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): sterile water - Test organisms (species):
- Apis mellifera
- Animal group:
- Hymenoptera (honeybees)
- Details on test organisms:
- TEST ORGANISM
- Common name: honey bee, Italien strain
- Source: California Agricultural Reserach (CAR) Inc. bee yard (hives originally created in 2000 from packaged bees shipped by Bear River Honey Company, Wheatland, CA.)
- Age at test initiation (mean and range, SD): 1 to 5 days
- Cultural background (if honeybees):
- Disease free: yes
- Kept according to standard practices: yes
ACCLIMATION
- Acclimation: CAR bee yard; prior to study start all hives were inventoried for their general health, vigor, and brood conditions
- Health during acclimation (any mortality observed): no - Study type:
- laboratory study
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- 4, 6, 24, and 48 h
- Test temperature:
- 26.73° to 35.79°C
- Humidity:
- 31% - 74%
- Details on test conditions:
- TEST SYSTEM
- Test container (material, size): cube-shaped, wire mesh cages, appr. 12.7 cm to a side, constructed of 3.2 mesh/cm2 hardware cloth
- Amount of soil or substrate:
- No. of organisms per container (treatment): 40 - 45
- No. of replicates per treatment group: 4
- No. of replicates per control: 4
- No. of replicates per vehicle control: 4
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : mortality
VEHICLE CONTROL PERFORMED: yes - Nominal and measured concentrations:
- 25 µL a.i./bee
- Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- LD0
- Effect conc.:
- 25 µg per animal
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- LD50
- Effect conc.:
- > 25 µg per animal
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Details on results:
- - Mortality at end of exposure period: zero
- Morphological abnormalities: none
- Behavioural abnormalities: none - Endpoint:
- toxicity to terrestrial arthropods: short-term
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Justification for type of information:
- Refer to category justification provided in IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Application method:
- contact
- Duration:
- 48 h
- Dose descriptor:
- LD0
- Effect conc.:
- 25 µg per animal
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Remarks on result:
- other:
- Remarks:
- Source, key, 1312-76-1, Richards 2006
- Duration:
- 48 h
- Dose descriptor:
- LD50
- Effect conc.:
- > 25 µg per animal
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Remarks on result:
- other:
- Remarks:
- Source, key, 1312-76-1, Richards 2006
Referenceopen allclose all
Under the conditions of this study, there was no evidence of harmful effects or increased mortality caused by acute contact with AgSil ¿ 25.
Description of key information
Key value for chemical safety assessment
Additional information
No test available on sodium silicate. Data considered here is read-across from potassium silicate based on an analogue-approach. In a GLP guideline study with honey bees by Richards (2006), following EPA OPPTS 850.3020 (Honey Bee Acute Contact Toxicity), for a potassium silicate solution (29.1 wt %) the 48 h LD0 and L50 were determined to be 25 ug and > 25 ug active matter per animal, respectively.
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