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EC number: 221-435-4 | CAS number: 3091-25-6
- 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

Immunotoxicity
Administrative data
- Endpoint:
- immunotoxicity: sub-chronic oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Data originally provided for the HPV programme, but study report it no longer available. Study summary provided for information purposes only.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 981
- Report date:
- 1981
Materials and methods
- Principles of method if other than guideline:
- Male and female rats were dosed in feed for 3 months with monooctyltin trichloride at 3, 10, 30, and 100 ppm.
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- Trichlorooctylstannane
- EC Number:
- 221-435-4
- EC Name:
- Trichlorooctylstannane
- Cas Number:
- 3091-25-6
- Molecular formula:
- C8H17Cl3Sn
- IUPAC Name:
- trichlorooctylstannane
- Details on test material:
- Monooctyltin Trichloride [CAS No. 3091-25-6]:Dioctyltin Dichloride [CAS No. 3542-36-7] (65:35% mixture)
Constituent 1
Test animals
- Species:
- rat
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- not specified
Doses / concentrations
- Remarks:
- Doses / Concentrations:
3, 10, 30, and 100 ppm
Basis:
no data
Results and discussion
Results of examinations
- Gross pathological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- ignificant reduction in thymus weight observed in males and females in the 100 ppm dose group. Marginal decrease observed at 30 ppm. No histopathological changes were observed in the thymic tissue.
- Details on results:
- GROSS PATHOLOGY
Significant reduction in thymus weight observed in males and females in the 100 ppm dose group. Marginal decrease observed at 30 ppm. No histopathological changes were observed in the thymic tissue.
Effect levels
open allclose all
- Dose descriptor:
- NOEL
- Effect level:
- 0.87 mg/kg bw/day
- Based on:
- not specified
- Sex:
- male
- Dose descriptor:
- NOEL
- Effect level:
- 0.88 mg/kg bw/day
- Based on:
- not specified
- Sex:
- female
Applicant's summary and conclusion
- Conclusions:
- A significant reduction in thymus weight was observed in males and females in the 100 ppm dose group with less apparent decrease in the 30 ppm group. No histopathological changes were observed in the thymic tissue.
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