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EC number: 200-854-6 | CAS number: 75-25-2
- 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

Hydrolysis
Administrative data
Link to relevant study record(s)
- Endpoint:
- hydrolysis
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Experimental Phase: 08 January 2018 to 29 June 2018. Report Issued: 28 August 2018.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- Duplicate sample solutions were taken initially and from the water bath samples at various time points. The pH of each solution was recorded. The concentration of test substance in the sample solutions was determined by high pressure liquid chromatography (HPLC). An aliquot of each sample solution was analysed as received.
Standards
Standard solutions of test item were prepared in acetonitrile : relevant pH buffer solution (1:99 v/v) to cover a nominal concentration range of 25 to 125 mg/L, with a duplicate at nominally 100 mg/L.
Matrix blank
Acetonitrile: relevant pH buffer solution (1:99 v/v). - Preliminary study:
- The extent of hydrolysis at pH 9 and 50 °C after 120 hours indicated that in accordance with the test guideline a further test (Tier 2) was required to estimate the rate constant and half-life at 25 °C.
- Transformation products:
- not measured
- Details on hydrolysis and appearance of transformation product(s):
- As the test item is bromoform, the hydrolysis products were considered to be dibromomethanol (CAS number: 166600-78-8) and aqueous hydrobromic acid (CAS number: 10035-10-6).
- Key result
- pH:
- 4
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Key result
- pH:
- 7
- Temp.:
- 25 °C
- DT50:
- > 1 yr
- Key result
- pH:
- 9
- Temp.:
- 25 °C
- Hydrolysis rate constant:
- 0 h-1
- DT50:
- > 1 yr
- Validity criteria fulfilled:
- yes
- Conclusions:
- The estimated half-life of the test substance at a pH of 4 or 7 is > 1 year at 25 °C. At pH 9 the test substance estimated rate constant and half-life at 25 °C is > 1 year.
- Executive summary:
Introduction
The study was conducted to determine the hydrolytic stability of the test substance at three pH’s. The method used was designed to be compatible with Method 111 of the OECD Guidelines for Testing of Chemicals, 13 April 2004.
Method
The test system consisted of buffer solutions at pH’s 4, 7 and 9. A preliminary test was performed where test substance solutions at pH 4, 7 and 9 were maintained at 50.0 ± 0.5 °C for a period of at least 240 hours.
Results from the Preliminary Test showed it was necessary to undertake further testing (Tier 2) at pH 9. for this further test solutions were maintained at 50.0 ± 0.5 °C, 60.0 ± 0.5 °C and 70.0 ± 0.5 °C for a period of at least 72 hours.
Results
The results were as follows:
pH Rate Constant (hr-1) Estimated half-life at 25 °C 4 - >1 year 7 - >1 year 9 7.96 x 10-6 > 1 year Conclusion
The estimated half-life of the test substance at a pH of 4 or 7 is > 1 year at 25 °C. At pH 9 the test substance estimated rate constant and half-life at 25 °C is > 1 year.
Reference
Description of key information
Hydrolytic stability of the test substance.
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1 yr
- at the temperature of:
- 25 °C
Additional information
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