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EC number: 212-039-2 | CAS number: 753-73-1
- 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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- not reported
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted in accordance with generally accepted scientific principles, possibly with incomplete reporting or methodological deficiencies, which do not affect the quality of the relevant results.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 977
- Report date:
- 1977
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 403 (Acute Inhalation Toxicity)
- Principles of method if other than guideline:
- The test was carried out in accordance with the below method.
K. Sachsse, L. Ullmann, G. Voss and R. Hess: Measurement of inhalation toxicity of aerosols in small laboratory animals. In: Proceedings of the Europ. Soc. for the Study of Drug Toxicity. Vol. XV, pp. 239-251, Zurich, June 1973. - GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Dimethyltin dichloride
- EC Number:
- 212-039-2
- EC Name:
- Dimethyltin dichloride
- Cas Number:
- 753-73-1
- Molecular formula:
- C2H6Cl2Sn
- IUPAC Name:
- dimethyltin dichloride
- Test material form:
- solid: crystalline
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Tif: RAIf (SPF)
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Raised on testing lab premises
- Weight at study initiation: 170 to 200 g
- Housing: Macrolon cages, type 4, (10 animals to a cage).
- Diet (e.g. ad libitum): NAFAG, Gossau SG ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: minimum of 4 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ± 1
- Humidity (%): 55 ± 5
- Photoperiod: 14 hrs dark / 10 hrs light
Administration / exposure
- Route of administration:
- inhalation: aerosol
- Type of inhalation exposure:
- nose only
- Vehicle:
- air
- Details on inhalation exposure:
- For inhalation the rats were kept on separate PVC tubes positioned radially around the exposure chamber such that snout and nostrils of the animals only were exposed to the aerosol.
The aerosol was generated by injecting a 50 % aqua test solution of the test material at a rate of 12, 30 and 60 ml/hour into an air stream which was discharged into the exposure chamber through a spray nozzle under a pressure of 2 atm. at a rate of 10 l/min.
The concentration and the particle size distribution of the aerosol in the vicinity of the animals was monitored at 1 hour intervals throughout the aerosol exposure. The concentration was determined gravimetrically by sampling the test atmosphere through a selectron filter of 50 mm diameter and with a pore size of 0.2 µm at an air flow rate of 10 l/min. The size distribution of the aerosol particles was measured with a Cascade Impactor with selectron filters of 25 mm diameter and with a pore size of 0.2 µm at an air flow rate of 17.5 l/min. - Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- 4 h
- Concentrations:
- 44 ± 6, 90 ± 7, 121 ± 3 and 167 ± 23 mg/m³.
Average concentration, gravimetrically determined. - No. of animals per sex per dose:
- 10 males, 10 females
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Other examinations performed: physical condition and incidence of death - Statistics:
- LC 50 including 95 % confidence limits was calculated by probit analysis method.
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- 115 mg/m³ air (analytical)
- Based on:
- act. ingr.
- 95% CL:
- 105 - 126
- Exp. duration:
- 4 h
- Mortality:
- 44 ± 6 mg/m³ : 0/10 males, 0/10 females within 14 days
90 ± 7 mg/m³ : 3/10 males, 1/10 females within 14 days
121 ± 3 mg/m³ : 5/10 males, 4/10 females within 14 days
167 ± 23 mg/m³ : 10/10 males, 10/10 females within 14 days - Clinical signs:
- other: Within 2 hours after starting the exposure the animals in concentrations where mortalities occurred showed dyspnoea, ventral position, tremor and ruffled fur. These symptoms became more accentuated as the concentration was increased. After the 4 hour expo
- Body weight:
- NDA
- Gross pathology:
- Dead Animals: Hemorrhages in the lungs were observed.
Sacrificed Animals: No substance related gross organ changes were seen.
Applicant's summary and conclusion
- Interpretation of results:
- other: Category 2: Fatal if inhaled
- Remarks:
- Criteria used for interpretation of results: EU
- Conclusions:
- Under the conditions of the test, the LC50 of a 4 hour aerosol exposure for rats of both sexes is 115 (105-126) mg/m³ air when evaluated for a 14 day post-treatment observation period.
- Executive summary:
The acute inhalation toxicity of dimethyltin dichloride was examined in a 4 hour study using male and female Tif: RAIf (SPF) rats, in a procedure similar to OECD 403.
Clinical observations included dyspnoea, ventral position, tremor and ruffled fur. These symptoms became more accentuated as the concentration was increased.
Hemorrhages in the lungs were observed in animals which died during the study, but not in those who survived.
The gravimetrically determined average concentrations used were 44 ± 6, 90 ± 7, 121 ± 3 and 167 ± 23 mg/m³.
The LC50 of a 4 hour aerosol exposure for rats of both sexes is 115 (105-126) mg/cm3 air, when evaluated for a 14 day post-treatment observation period.
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