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EC number: 240-474-8 | CAS number: 16423-68-0
- 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
Endpoint summary
Administrative data
Description of key information
Biodegradation in water:
28-days Manometric respirometry test was conducted following the OECD guideline 301F to determine the ready biodegradability of the test chemical. The study was performed at a temperature of 20 ± 1°C. Mixture of domestic waste water, surface soil and soil samples was used as a test inoculum for the study. This inoculum was collected and were mixed to get diluted suspension. The inoculum was kept aerobic until being used for experiment by supplying organic and inorganic sources required by micro flora to sustain at controlled laboratory conditions. This gave the bacterial count as 107to 108 CFU/ml. At the regular interval microbial plating was also performed on agar to confirm the vitality and CFU count of microorganism. OECD mineral medium was used for the study. The test system included control, test item and reference item. The concentration of test and reference item (Sodium Benzoate) chosen for both the study was 100mg/L, while that of inoculum was 10ml/l. ThOD (Theoretical oxygen demand) of test and reference item was determined by calculation. % Degradation was calculated using the values of BOD and ThOD for test chemical and reference chemical. The % degradation of procedure control (reference item) was also calculated using BOD & ThOD and was found to be 77.36%. The mean BOD values (mg O2/l) in control on 28th day was 28.2 mg O2/l, thereby fulfilling the control validity criteria (i.e., the oxygen consumption of the inoculum blank is normally 20-30 mg O2/l and should not be greater than 60 mg/l in 28 days). Degradation of Sodium Benzoate exceeds 60% after 14 days. The activity of the inoculums is thus verified and the test can be considered as valid. The BOD28 value of test chemical was observed to be 0.058 mgO2/mg. ThOD was calculated as 0.709 mgO2/mg. Accordingly, the % degradation of the test chemical after 28 days of incubation at 20 ± 1°C according to manometric respirometry test was determined to be 8.18%. Thus, the test chemical can be considered as not readily biodegradable.
Biodegradation in water: Simulation test:
Estimation Programs Interface prediction model was run to predict the half-life in water for the test chemical. If released in to the environment, 4.74 % of the chemical will partition into water according to the Mackay fugacity model level III and the half-life period of test chemical in water is estimated to be 180 days (4320 hrs). The half-life 180 days estimated by EPI suite indicates that the chemical is persistent in water and the exposure risk to aquatic animals is moderate to high.
Biodegradation in sediment: Simulation test:
Estimation Programs Interface prediction model was run to predict the half-life in sediment for the test chemical. If released in to the environment, 9.39 % of the chemical will partition into sediment according to the Mackay fugacity model level III and the half-life period of test chemical in sediment is estimated to be 1620.8 days (38900 hrs). The half-life 1620.8 days estimated by EPI suite indicates that the chemical is persistent in sediment and the exposure risk to aquatic animals is moderate to high.
Biodegradation in soil:
The half-life period of test chemical in soil was estimated using Level III Fugacity Model by EPI Suite version 4.1 estimation database (EPI suite). If released into the environment, 85.8 % of the chemical will partition into soil according to the Mackay fugacity model level III. The half-life period of test chemical in soil is estimated to be 360 days (8640 hrs). Based on this half-life value of test chemical, it is concluded that the chemical is persistent in the soil environment and the exposure risk to soil dwelling animals is moderate to high.
Additional information
Biodegradation in water:
28-days Manometric respirometry test was conducted following the OECD guideline 301F to determine the ready biodegradability of the test chemical. The study was performed at a temperature of 20 ± 1°C. Mixture of domestic waste water, surface soil and soil samples was used as a test inoculum for the study. This inoculum was collected and were mixed to get diluted suspension. The inoculum was kept aerobic until being used for experiment by supplying organic and inorganic sources required by micro flora to sustain at controlled laboratory conditions. This gave the bacterial count as 107to 108 CFU/ml. At the regular interval microbial plating was also performed on agar to confirm the vitality and CFU count of microorganism. OECD mineral medium was used for the study. The test system included control, test item and reference item. The concentration of test and reference item (Sodium Benzoate) chosen for both the study was 100mg/L, while that of inoculum was 10ml/l. ThOD (Theoretical oxygen demand) of test and reference item was determined by calculation. % Degradation was calculated using the values of BOD and ThOD for test chemical and reference chemical. The % degradation of procedure control (reference item) was also calculated using BOD & ThOD and was found to be 77.36%. The mean BOD values (mg O2/l) in control on 28th day was 28.2 mg O2/l, thereby fulfilling the control validity criteria (i.e., the oxygen consumption of the inoculum blank is normally 20-30 mg O2/l and should not be greater than 60 mg/l in 28 days). Degradation of Sodium Benzoate exceeds 60% after 14 days. The activity of the inoculums is thus verified and the test can be considered as valid. The BOD28 value of test chemical was observed to be 0.058 mgO2/mg. ThOD was calculated as 0.709 mgO2/mg. Accordingly, the % degradation of the test chemical after 28 days of incubation at 20 ± 1°C according to manometric respirometry test was determined to be 8.18%. Thus, the test chemical can be considered as not readily biodegradable.
Biodegradation in water: Simulation test:
Estimation Programs Interface prediction model was run to predict the half-life in water for the test chemical. If released in to the environment, 4.74 % of the chemical will partition into water according to the Mackay fugacity model level III and the half-life period of test chemical in water is estimated to be 180 days (4320 hrs). The half-life 180 days estimated by EPI suite indicates that the chemical is persistent in water and the exposure risk to aquatic animals is moderate to high.
Biodegradation in sediment: Simulation test:
Estimation Programs Interface prediction model was run to predict the half-life in sediment for the test chemical. If released in to the environment, 9.39 % of the chemical will partition into sediment according to the Mackay fugacity model level III and the half-life period of test chemical in sediment is estimated to be 1620.8 days (38900 hrs). The half-life 1620.8 days estimated by EPI suite indicates that the chemical is persistent in sediment and the exposure risk to aquatic animals is moderate to high.
Biodegradation in soil:
The half-life period of test chemical in soil was estimated using Level III Fugacity Model by EPI Suite version 4.1 estimation database (EPI suite). If released into the environment, 85.8 % of the chemical will partition into soil according to the Mackay fugacity model level III. The half-life period of test chemical in soil is estimated to be 360 days (8640 hrs). Based on this half-life value of test chemical, it is concluded that the chemical is persistent in the soil environment and the exposure risk to soil dwelling animals is moderate to high.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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