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EC number: 231-748-8 | CAS number: 7719-09-7
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP guideline stuy
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 013
- Report date:
- 2013
Materials and methods
- Objective of study:
- other: hydrolysis study
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OECD TG 111
- Principles of method if other than guideline:
- The test was performed according to the OECD Guidelines for Testing of Chemicals, Section 1 – Physical-Chemical Properties, OECD TG 111 (2004). As the hydrolysis was known to occur rapidly, hydrolysis behaviour of the test item in aqueous solutions was investigated in a Tier 1 test at room temperature instead of 50 °C, at pH 4, pH 7 and pH 9.
The hydrolysis behaviour was monitored by ion chromatography analysis with conductivity detection.
For further details see study endpoint summary of this study in IUCLID chapter 5.1.2.: hydrolysis. - GLP compliance:
- yes
Test material
- Reference substance name:
- Thionyl dichloride
- EC Number:
- 231-748-8
- EC Name:
- Thionyl dichloride
- Cas Number:
- 7719-09-7
- Molecular formula:
- Cl2OS
- IUPAC Name:
- thionyl dichloride
- Test material form:
- other: liquid
- Details on test material:
- purity: 99.6%
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- other: not applicable - hydrolysis study
- Strain:
- other: not applicable - hydrolysis study
Administration / exposure
- Route of administration:
- other: not applicable - hydrolysis study
- Vehicle:
- other: not applicable - hydrolysis study
- Duration and frequency of treatment / exposure:
- not applicable - hydrolysis study
Doses / concentrations
- Remarks:
- Doses / Concentrations:
not applicable - hydrolysis study
- No. of animals per sex per dose / concentration:
- not applicable - hydrolysis study
- Control animals:
- other: not applicable - hydrolysis study
Results and discussion
Main ADME results
- Type:
- other: hydrolysis study in aqueous solution;
- Results:
- The hydrolysis half time (t 1/2) of thionyl dichloride is < 2 minutes at 23°C and different pH (4, 7 or 9)
Toxicokinetic / pharmacokinetic studies
- Details on absorption:
- not applicable - hydrolysis study
- Details on distribution in tissues:
- not applicable - hydrolysis study
- Details on excretion:
- not applicable - hydrolysis study
Bioaccessibility (or Bioavailability)
- Bioaccessibility (or Bioavailability) testing results:
- not applicable - hydrolysis study
Any other information on results incl. tables
Theoretical hydrolysis of Thionylchlorid:
SOCl2 + H2O -> 2 HCl + SO2
In the hydrolysis test solutions chloride and the water adduct / oxidation products sulfite and sulfate of the hydrolysis product sulfur dioxide were determined by ion chromatography.
Sulfur dioxide could not be detected by ion chromatography.
The test item shows rapid hydrolysis at pH 4, pH 7 and pH 9 within a few minutes.
Chloride, sulfite and sulfate as the only by ion chromatography detectable hydrolysis products were identified by comparison with the retention time of the calibration substances.
The concentrations of the formed chloride in the hydrolysis test solutions were determined by external calibration method and correspond to the theoretical values assuming a complete degradation of the test item (recovery 99.1 to 102.4 %). Sulfite and sulfate were quantified accordingly. Recoveries were in the range of 80 to 95 %.
Losses of sulphur might be explained by the evaporation of gaseous sulphur dioxide.
Due to the observed immediately and complete degradation (100 %) of the test item between sample preparation time and injection time by ion chromatography, the following half-life time and hydrolysis rate was calculated at 23 °C (room temperature) and pH 4, pH 7 and pH 9.
Test at 23 °C and pH 4: Half-life-time: t(1/2) = 72 seconds
Hydrolysis rate constant: k = 9.59410 x 10E-3 per sec
The half-life time is set to: t ½ < 2 minutes
Test at 23 °C and pH 7: Half-life-time: t(1/2) = 72 seconds
Hydrolysis rate constant: k = 9.59410 x 10E-3 per sec
The half-life time is set to: t ½ < 2 minutes
Test at 23 °C and pH 9: Half-life-time: t(1/2) = 54 seconds
Hydrolysis rate constant: k = 1.27921 x 10E-2 per sec
The half-life time is set to: t ½ < 2 minutes
Applicant's summary and conclusion
- Executive summary:
The test was performed according to the OECD Guidelines for Testing of Chemicals, Section 1 – Physical-Chemical Properties, OECD TG 111 (2004). As the hydrolysis was known to occur rapidly, hydrolysis behaviour of the test item in aqueous solutions was investigated in a Tier 1 test at room temperature instead of 50 °C, at pH 4, pH 7 and pH 9.
The hydrolysis behaviour was monitored by ion chromatography analysis with conductivity detection.
The hydrolysis half time (t 1/2) at 23°C and pH 4, pH 7, and pH 9 is < 2 minutes
For further details see study endpoint summary of this study in IUCLID chapter 5.1.2.: hydrolysis.
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