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EC number: 232-038-0 | CAS number: 7783-96-2
- 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
Endpoint summary
Administrative data
Description of key information
There is no acute toxicity data available for silver iodide. Read-across is applied to other comparable silver substance.
The most comparable compounds is AgCl, a LD50 oral of > 5110 mg/kg bw (equivalent to 8370.6 mg/kg bw of silver iodide) has been determined. it is noted that the solubility of AgI (30µg/L) is even lower than for AgCl (1.9 mg/L). Testing for acute oral toxicity for AgI is thus not considered to be scientifically justified.
Note: Acute toxicity study via dermal and inhalation route are not a requirement under Annex VII of Regulation 1907/2006.
Key value for chemical safety assessment
Acute toxicity: via oral route
Link to relevant study records
- Endpoint:
- acute toxicity: oral
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- Substance considered to fall within the scope of the read-across: justification of a read-across approach for human health hazard endpoint (document attached in IUCLID section 13).
- Reason / purpose for cross-reference:
- read-across source
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 8 370.6 mg/kg bw
- Remarks on result:
- other: 5110 mg of silver chloride is equivalent to 8370.6 mg of silver iodide
- Mortality:
- Deaths did not occur.
- Clinical signs:
- other: The signs of toxicity were slight to moderate hypokinesia, stilted gait, piloerection, sunken sides, vocalization on handling, red crusted noses, and diarrhea with black discoloured feces. Individual rats additionally showed chromodacryorrhea and strenuou
- Gross pathology:
- At necropsy no changes were recorded.
Brain and spinal cord of the female rat that did not recover completely were examined microscopically, but changes could not be detected. - Other findings:
- Diarrhea was caused by the vehicle alone, too.
- Interpretation of results:
- GHS criteria not met
- Remarks:
- Silver iodide is not toxic
- Conclusions:
- The LD 50 values for silver chloride (silver iodide) tested in a single dose were above 5110 (8370.6) mg/kg for male and female rats (limit test).
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- > 8 370.6 mg/kg bw
- Quality of whole database:
- reliable database
Additional information
Justification for classification or non-classification
- Zechel et al 1989 performed a reliable in-vivo acute toxicity study performed via oral route (OECD 401 – GLP) with solid powder (purity 75% of Ag). The study concluded that silver chloride is not acute toxic via oral route. The LD50 was defined by the author at > 5110 mg/kg bw. It then concluded that silver iodide is not acute toxic via oral route.
There is no reliable and relevant data available for silver iodide (AgI). A read-across with silver chloride (AgCl) is applied. It is noted that the solubility of AgI (30 µg/L) is even lower than AgCl (1.9 mg/L).
In consequence, silver iodide does not require classification for acute toxicity endpoints.
Note: Acute toxicity study via dermal and inhalation route are not a requirement under Annex VII of Regulation 1907/2006.
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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