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EC number: 201-039-8 | CAS number: 77-58-7
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Not stated
- 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:
- 2 004
- Report date:
- 2004
Materials and methods
- Objective of study:
- other: to simulate the hydrolytic action by mammalian gastric contents and to determine if the tin-ligand bond breaks, leading to formation of the corresponding alkyltin chloride and release of the ligand.
- Principles of method if other than guideline:
- No further information required.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Dibutyltin dilaurate
- EC Number:
- 201-039-8
- EC Name:
- Dibutyltin dilaurate
- Cas Number:
- 77-58-7
- Molecular formula:
- C32H64O4Sn
- IUPAC Name:
- dibutyltin dilaurate
- Details on test material:
- - Name of test material (as cited in study report): Dibutyltin dilaurate (DBTL)
- Molecular formula (if other than submission substance): (C4H9)2S(C12H23O2)2
- Molecular weight (if other than submission substance): 631.55
- Analytical purity: 98.2%
- Lot No: 0020
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- other: No species were used - simulated gastric hydrolysis
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- DBTL was tested under low pH (~1-2) conditions (0.07 N HCl) at 37 degrees Celsius in order to simulate they hydrolytic action by mammalian gastric contents. The degree of hydroloysis for the test substance was studied by determination of the amount of DBTC formed after 0.5, 1, 2, and 4 hours, uusing GC-FPD.
Administration / exposure
- Route of administration:
- other: test to simulate mammalian gastric contents
- Vehicle:
- other: insoluble in solvent; 'diluted' by thoroughly mixing with 811.17 mg of lactose
- Details on exposure:
- No information available.
- Duration and frequency of treatment / exposure:
- No information available.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
50 ul of the stock solution of DBTL (5.15 mg/ml) was added to 25 ml of 0.07 N HCl.
- No. of animals per sex per dose / concentration:
- No information available.
- Control animals:
- no
- Positive control reference chemical:
- No further information required.
- Details on study design:
- Into a series of 4 polypropylene vessels, 50 ul of the stock solution of DBTL (5.15 mg/ml) was added to 25 ml of 0.07 N HCl (already at 37 degrees Celsius). In this way, the concentration of DBTL in the final 0.07 N HCl solution was 10.31 mg/L. The solution was stirred for predetermined 37 degrees C, and the temperature was maintained using an oven.
- Details on dosing and sampling:
- A sample was taken from one of the Teflon vessels after 0.5, 1, 2, and 4 hours. Once a vessel was sampled, no other sample was collected from that vessel. Experiments were performed in duplicate.
- Statistics:
- The percentage of hydrolyzed organotin test substance based on the DBTC measurement was calculated as follows: The total amount of DBTC in solution that can be formed upon complete hydrolysis of the test substance was approximately 4.96 mg/l. This level was calculated using the following formula:
50 (ul) * 5.15 (mg/ml)/25 ml * Mw(DBTC)/Mw(DBTL).
Results and discussion
- Preliminary studies:
- The mean percentage of hydrolysis of DBTL is summarized in Table 6 (see below). Under chemical conditions intended to simulate mammalian gastric contents, as described in this report, DBTL to DBTC was rapid. The percentage of hydrolysis was 87.8% after 2 hours. The half-life was < 0.5 hours
Toxicokinetic / pharmacokinetic studies
- Details on absorption:
- No information available.
- Details on distribution in tissues:
- No information available.
- Details on excretion:
- No information available.
Toxicokinetic parameters
- Toxicokinetic parameters:
- half-life 1st: <0.5 hours
Metabolite characterisation studies
- Metabolites identified:
- yes
- Details on metabolites:
- The percentage of hydrolyzed organotin test substance was determined. Most of the DBTL was hydrolyzed to DBTC in 2 hours.
Any other information on results incl. tables
Table 6: summary of the results of the simulated gastric hydrolysis
Time (h) | Mean % of hydrolysis (DBTC values) (%) | Mean % of hydrolysis (Lauric acid values) (%) |
0.5 | 82.3 | 21.5 |
1 | 77.9 | 7.4 |
2 | 87.8 | 11.2 |
4 | 87.1 | 23.4 |
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): other: DBTL may be hydrolyzed to a great extent in simulated mammalian gastric contents
Under chemical conditions intended to simulate mammalian gastric contents, for DBTL the percent hydrolysis was 87.8% after two hours and the half life was < 0.5 hours. - Executive summary:
Dibutyltin laurate was tested under pH 1 -2 conditions (0.07 N HCl) at 37 degrees C in order to simulate the hydrolytic action by mammalian gastic contents. The hypothesis was that in the hdrochloric acid solution, the tin-ligand bond breaks, leading to formation of the corresponding alkyltin chloride and simultaneous liberation of the ligand. The degree of hydrolysis was tested by GC-FPD. Where possible, the ligand was also analyzed. The ligand was analysed by GC-MS. DBTL was hydrolysed to DBTC by 87.8% after 2 hours. The half-life was <0.5 hours.
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