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EC number: 221-110-7 | CAS number: 3006-82-4
- 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:
- 2010-05-21 to 2010-08-04
- 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)
- Version / remarks:
- 2004
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.7 (Degradation: Abiotic Degradation: Hydrolysis as a Function of pH)
- Version / remarks:
- 2008
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- The samples were measured by the previously validated reverse phase HPLC method using UV detection .
- Buffers:
- - pH 4: 3 mL 0.2 M Sodium hydroxide and 375 mL 0.2 M Potassium hydrogen phthalate were diluted to 1500 mL with ultra-pure water,
- pH 7: 221.7 mL 0.2 M Sodium hydroxide and 375 mL 0.2 M Potassium dihydrogen phosphate were diluted to 1500 mL with ultra-pure water,
- pH 9: 160.5 mL 0.2 M Sodium hydroxide and 375 mL 0.2 M Boric acid and Potassium chloride were diluted to 1500 mL with ultra-pure water. - Details on test conditions:
- TEST SYSTEM
- Measures taken to avoid photolytic effects: The hydrolysis reaction was carried out using a dark thermostat to avoid photolytic effects.
- Measures to exclude oxygen: Nitrogen was bubbled into the water for five minutes before the preparation of the solutions in order to exclude oxygen.
TEST SOLUTION
Stock solution (~5 mg/mL): ca.50 mg of the test item was dissolved in acetonitrile to a total volume of 10 mL. The test solutions were prepared by dilution of the “stock solutions for the hydrolysis test” with the corresponding buffer solutions, just before analysis and start of the storage. 1500 mL sterile solutions were prepared at pH 4, 7 and 9. Solutions were transferred into ~22 mL screw-cap glass tubes with PTFE septa. The solution was analysed at the start of the tests and then at appropriate time intervals: in order to get at least six other data points in the range of 10 to 90 % hydrolysis. The test solutions were prepared by five-hundred fold dilution of the “stock solutions for the hydrolysis test” with the corresponding buffer solutions. - Duration:
- 5 d
- pH:
- 4
- Initial conc. measured:
- ca. 22 mg/L
- Duration:
- 5 d
- pH:
- 7
- Initial conc. measured:
- ca. 22 mg/L
- Duration:
- 5 d
- pH:
- 9
- Initial conc. measured:
- ca. 22 mg/L
- Number of replicates:
- 2
- Negative controls:
- yes
- Remarks:
- control buffer
- Statistical methods:
- No statistical method performed.
- Preliminary study:
- Based on the results of the preliminary test the hydrolysis rate of TBPEH was found to be 70 % at pH 4 and 75 % at pH 7 and 84 % at pH 9 after 5 days at 50 degree C.
- Transformation products:
- no
- Details on hydrolysis and appearance of transformation product(s):
- The decomposition of the substance was monitored by HPLC-UV. The decomposition of the test substance TBPEH is well known and results in the formation of tert-butanol and 2-ethylhexanoic acid as the main compounds. However, these degradation products can not be detected under the given validated test method neither from the decomposition chromatograms nor by using the corresponding reference substances.
The LCQ analyse of the decomposition solution did not provide any additional information on the degradation products. - % Recovery:
- 87
- pH:
- 4
- Temp.:
- 25 °C
- Duration:
- 5 d
- % Recovery:
- 85
- pH:
- 7
- Temp.:
- 25 °C
- Duration:
- 5 d
- % Recovery:
- 92
- pH:
- 9
- Temp.:
- 25 °C
- Duration:
- 5 d
- Key result
- pH:
- 4
- Temp.:
- 15 °C
- Hydrolysis rate constant:
- 0.007 h-1
- DT50:
- 104 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 4
- Temp.:
- 37 °C
- Hydrolysis rate constant:
- 0.017 h-1
- DT50:
- 41 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 4
- Temp.:
- 60 °C
- Hydrolysis rate constant:
- 0.042 h-1
- DT50:
- 17 h
- Type:
- (pseudo-)first order (= half-life)
- Key result
- pH:
- 7
- Temp.:
- 15 °C
- Hydrolysis rate constant:
- 0.008 h-1
- DT50:
- 86 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 7
- Temp.:
- 37 °C
- Hydrolysis rate constant:
- 0.012 h-1
- DT50:
- 60 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 7
- Temp.:
- 60 °C
- Hydrolysis rate constant:
- 0.041 h-1
- DT50:
- 17 h
- Type:
- (pseudo-)first order (= half-life)
- Key result
- pH:
- 9
- Temp.:
- 15 °C
- Hydrolysis rate constant:
- 0.005 h-1
- DT50:
- 152 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 9
- Temp.:
- 37 °C
- Hydrolysis rate constant:
- 0.008 h-1
- DT50:
- 84 h
- Type:
- (pseudo-)first order (= half-life)
- pH:
- 9
- Temp.:
- 60 °C
- Hydrolysis rate constant:
- 0.061 h-1
- DT50:
- 11 h
- Type:
- (pseudo-)first order (= half-life)
- Details on results:
- No further details
- Validity criteria fulfilled:
- yes
- Conclusions:
- The calculated half lives of the hydrolysis reactions at pH 4, pH 7 and pH 9 are as follows:
t 1/2 at pH4 and 15 degree C: 104 h, 37 degree C: 41 h, 60 degree C: 17 h;
t 1/2 at ph7 and 15 degree C: 86 h, 37 degree C: 60 h, 60 degree C: 17 h;
t 1/2 at pH9 and 15 degree C: 152 h, 37 degree C: 84 h, 60 degree C: 11 h.
Based on the results obtained, test substance tert.-Butylperoxy- 2-ethylhexanoat is hydrolytically unstable at pH 4, pH 7 and pH 9 under the conditions investigated. - Executive summary:
The hydrolysis of tert.-Butylperoxy- 2-ethylhexanoat in different pH buffer solutions was investigated according to OECD Guideline No. 111 and EU method C.7. The analysis of tert.-Butylperoxy- 2-ethylhexanoat was carried out with a HPLC method using UV detection. Sterile aqueous buffer solutions of different pH values (pH 4, 7, 9) were prepared with the test substance solutions and buffer solutions. The hydrolysis of TBPEH was examined at pH 4, 7 and 9 at three temperatures: 15 ± 0.5 degree C, 37 ± 0.5 degree C and 60 ± 0.5 degree C. TBPEH concentrations in the buffer solutions were: ca. 22 mg/L (ca. 0.1 mM). The calculated half lives of the hydrolysis reactions at pH 4, pH 7 and pH 9 are given in the following table:
Buffer solution
Temperature, °C
t1/2, hours
pH 4
15
104
25
67
37
41
60
17
pH 7
15
86
25
67
37
60
60
17
pH 9
15
152
25
103
37
84
60
11
Based on the results obtained, test substance tert.-Butylperoxy- 2-ethylhexanoat hydrolytically unstable at pH 4, pH 7 and pH 9 under the conditions investigated.
Reference
No other information
Description of key information
The hydrolysis of TBPEH was determined at various pH values and temperatures. The rate of hydrolysis decreased with increasing pH and temperature. Hydrolysis increased with temperature and decreasing pH. From values obtained in the key study, the environmentally relevant rate of hydrolysis at pH 7 and 12 °C was calculated using the Arrhenius equation and resulted in a hydrolysis rate of 1.84E 03 h 1 and a DT50 of 376.3 h (15.68 days).
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 15.8 d
- at the temperature of:
- 12 °C
Additional information
The hydrolysis behaviour of TBPEH was assessed in two studies according to EU method C.7 and OECD guideline no. 111. From values obtained in the key study, the environmentally relevant rate of hydrolysis at pH 7 and 12 °C was calculated using the Arrhenius equation and resulted in a hydrolysis rate of 1.84E 03 h 1 and a DT50 of 376.3 h (15.68 days).
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