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EC number: 257-581-0 | CAS number: 51988-14-8
- 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:
- until 08 May 2017
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 111 (Hydrolysis as a Function of pH)
- Deviations:
- yes
- Remarks:
- No buffer solution has been used and the test was performed without pH control and at room temperature.
- GLP compliance:
- no
- Remarks:
- Test was performed scientifically reasonable and was well-documented, and the sponsor is considered most suitable to perform this test due to the extensive knowledge of the substance, although not having GLP-status.
- Radiolabelling:
- no
- Analytical monitoring:
- yes
- Details on sampling:
- - Sampling intervals for the parent/transformation products / Sampling method: 10 mg of the test substance were dissolved in 2 mL THF and filled up to 100 mL with methanol. 10 mL of this stock solution were transferred into a 1 L volumetric flask and filled up to 1 L with water (c = 1 ppm). This test solution was directly subjected to HPLC measurements about every 20 min in order to follow hydrolysis.
- Buffers:
- none
- Details on test conditions:
- TEST SYSTEM
- Type, material and volume of test flasks, other equipment used: 10 mg of the test substance were dissolved in 2 mL THF and filled up to 100 mL with methanol. 10 mL of this stock solution were transferred into a 1 L volumetric flask and filled up to 1 L with water (c = 1 ppm). This test solution was directly subjected to HPLC measurements about every 20 min in order to follow hydrolysis. - Duration:
- 12.85 h
- Temp.:
- 20 °C
- Initial conc. measured:
- 1 mg/L
- Remarks:
- Since the instability of the test substance in water is known a preliminary test was omitted. The test was performed at T = 20 ± 2 °C. The pH value of the test solution was not determined.
- Number of replicates:
- 1
- Positive controls:
- no
- Negative controls:
- no
- Statistical methods:
- In order to determine half-life the logarithmic peak areas normalised to the initial peak area were plotted against time. The quantification was done by area normalisation.
- Test performance:
- The HPLC chromatograms showed rapid degradation of the substance in water at room temperature. 1,3,4-Dimercaptothiadiazol (DMTD) and benzoic acid were identified as degradation products as expected by hydrolytical cleavage of the thioester group. The identification of the degradation products was done by diode array detector and comparison of the obtained UV spectra with a spectral library.
For testing of pseudo-first order kinetics the logarithm of the normalised peak area was plotted against time. A linear relationship was obtained (Coefficient of correlation R² = 0.9791). The half-life time of the test item was determined according to the model for pseudo-first order reaction. The slope of the linear regression was constructed excluding the last data points at t = 10.33 min and following. - Transformation products:
- yes
- No.:
- #1
- No.:
- #2
- Details on hydrolysis and appearance of transformation product(s):
- The hydrolytic degradation of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate can be described as a pseudo-first order kinetic and the half-life of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate was determined to be 1.91 h. 1,3,4-Dimercapto-thiadiazol (DMTD, CAS 1072-71-5) and benzoic acid (CAS 65-85-0) were identified as degradation products as expected by hydrolytical cleavage of the thioester group. No further assessment of the hydrolysis of benzoic acid and DMTD has been conducted because these substances are known to be hydrolytically stable.
- Key result
- Temp.:
- 20 °C
- Hydrolysis rate constant:
- 0.36 h-1
- DT50:
- 1.91 h
- Type:
- (pseudo-)first order (= half-life)
- Details on results:
- The HPLC chromatograms showed rapid degradation of the substance in water at room temperature. 1,3,4-Dimercaptothiadiazol (DMTD) and benzoic acid were identified as degradation products as expected by hydrolytical cleavage of the thioester group. The identification of the degradation products was done by diode array detector and comparison of the obtained UV spectra with a spectral library.
For testing of pseudo-first order kinetics the logarithm of the normalised peak area was plotted against time. A linear relationship was obtained (Coefficient of correlation R² = 0.9791). The half-life time of the test item was determined according to the model for pseudo-first order reaction. The slope of the linear regression was constructed excluding the last data points at t = 10.33 min and following. - Validity criteria fulfilled:
- not specified
- Conclusions:
- The study was conducted scientifically reasonable according to OECD TG 111 with minor deviations and is sufficiently documented. Hence, it is sufficiently reliable to assess the hydrolysis behaviour of 5-Mercapto-1,3,4-thiadiazole-2-thiol-benzoate in unbuffered water. The hydrolytic degradation of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate can be described as a pseudo-first order kinetic and the half-life of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate was determined to be 1.91 h. 1,3,4-Dimercapto-thiadiazol (DMTD, CAS 1072-71-5) and benzoic acid (CAS 65-85-0) were identified as degradation products as expected by hydrolytical cleavage of the thioester group. No further assessment of the hydrolysis of benzoic acid and DMTD needed to be conducted because these substances are known to be hydrolytically stable.
It can be concluded that the substance hydrolyzes very rapidly in water, i.e. the half life is max. 1/25 of the test duration when put into aqueous test systems, e.g. daphnia or algae acute toxicity tests. Hence, the substance as such does not need to be tested in those systems, it is sufficient for hazard assessment to use data gained with 1,3,4-Dimercapto-thiadiazol (DMTD, CAS 1072-71-5) and benzoic acid (CAS 65-85-0). - Executive summary:
The substance 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate is known to hydrolyse in aqueous solutions. Thus, a hydrolysis test was performed and hydrolysis products were identified. The test design was according to the principles of the guideline OECD 111. No buffer solution has been used and the test was performed without pH control and at room temperature.
The hydrolytic degradation of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate can be described as a pseudo-first order kinetic and the half-life of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate was determined to be 1.91 h. 1,3,4-Dimercapto-thiadiazol (DMTD, CAS 1072-71-5) and benzoic acid (CAS 65-85-0) were identified as degradation products as expected by hydrolytical cleavage of the thioester group. No further assessment of the hydrolysis of benzoic acid and DMTD has been conducted because these substances are known to be hydrolytically stable.
Reference
Description of key information
Hydrolysis: OECD 111, half life: 1.19h at 20 °C
Key value for chemical safety assessment
- Half-life for hydrolysis:
- 1.91 h
- at the temperature of:
- 20 °C
Additional information
The substance 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate is known to hydrolyse in aqueous solutions. Thus, a hydrolysis test was performed and hydrolysis products were identified. The test design was according to the principles of the guideline OECD 111. No buffer solution has been used and the test was performed without pH control and at room temperature.
The hydrolytic degradation of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate can be described as a pseudo-first order kinetic and the half-life of 5-mercapto-1,3,4-thiadiazole-2-thiol-benzoate was determined to be 1.91 h. 1,3,4-Dimercapto-thiadiazol (DMTD, CAS 1072-71-5) and benzoic acid (CAS 65-85-0) were identified as degradation products as expected by hydrolytical cleavage of the thioester group. No further assessment of the hydrolysis of benzoic acid and DMTD has been conducted because these substances are known to be hydrolytically stable.
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