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EC number: 293-316-5 | CAS number: 91053-50-8
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Elkton, Maryland (U.S.A.) Publically Owned Treatment Works (POTW)
- Storage conditions: glass containers under aerobic conditions in the period between sampling and application on return to the laboratory
To each of the test vessels needed to conduct the study, a total volume of 3 L was added as follows: 1) Test water: 2861 mL; 2) Solution A: 30 mL; 3) Solution B, C, and D: 3 mL; 4) Inoculum: 17.00 mL. This mixture was aerated with CO2-free air for one day to purge the system of carbon dioxide. After the aeration period, test and reference substances were added using the final 83.0 mL of test water for quantitative transfer of the test and reference substances to bring the final volume to 3 litres. The 83.0 mL of test water was also added to the inoculum control blanks. Three CO2 gas diffusion bottles were filled with 100 mL of 0.0125 M Ba(OH)2 solution and connected in series to the exit air line of each 4 L vessel. The pH of each test vessel was measured and recorded. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 20 other: mg C/L
- Parameter followed for biodegradation estimation:
- CO2 evolution
- Details on study design:
- TEST CONDITIONS
- Composition of medium: 20 mg C/L
- pH: measured on days 0 and 25
TEST SYSTEM
- Reference Substance Name: Benzoic acid, sodium salt, purity: 99.9%
- Mineral Media Stock Solutions: 1) Mineral Medium Stock Solution A: 4.25 g KH2PO4 + 10.88 g K2HPO4 + 16.70 g Na2HPO4•2H2O + 0.25 g NH4Cl added to 0.5L-1 of water, 2) Mineral Medium Stock Solution B: 13.75g CaCl2 added to 0.5 L-1 of water, 3) Mineral Medium Stock Solution C: 11.25 g MgSO4.7H2O added to 0.5 L-1 of water, 4) Mineral Medium Stock Solution D: 0.25 g FeCl3•6H2O added to 1.0 L-1 of water.
The biological system used was secondary activated sludge from the Elkton, Maryland (U.S.A) Publicly-Owned Treatment Works (POTW). The biodegradation process was monitored on days 1, 4, 6, 8, 12, 18 and 25 when carbon dioxide (CO2) trapped in barium hydroxide was measured by titration of the residual hydroxide. Additionally, traps were titrated on day 26 to quantify any remaining CO2 after acidifying the test systems on day 25. The amount of CO2 produced from the test substance (corrected for that from the Inoculum Control Blank) is expressed as a percentage of the total CO2 that the test substance could have theoretically produced (ThCO2) based on the measured total carbon (TC) content of the test substance. - Reference substance:
- benzoic acid, sodium salt
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 72.5
- Sampling time:
- 25 d
- Parameter:
- % degradation (CO2 evolution)
- Value:
- 60
- Sampling time:
- 12 d
- Details on results:
- The ThCO2 produced by the test and reference substances was determined to be 2.55 and 2.14 mg CO2/mg substance, respectively (see Table 1). The value for the test substance was determined by measuring its total carbon content. The value for the reference substance was determined using its molecular formula and the purity because the composition was known.
In the test, the following results (see Table 2) were observed: 1) the test substance reached a final biodegradability of 72.5% on day 25. Since biodegradability was >60% by day 12 and reached this level within 10 days of reaching 10%, this chemical is considered “Ready Biodegradable”, and 2) Sodium benzoate (the reference substance) was greater than 60% biodegradable within 14 days confirming that the inoculum was viable.
In the Toxicity Control, which included the test and reference substances in the same vessel, biodegradation was greater than 25% within 14 days. Therefore the test substance was not inhibitory to microorganisms in the inoculum.
The lag phase of the test substance was from the start of the test until about day two. The lag phase is the period from inoculation until the degradation percentage has increased to 10%. There was a well-defined degradation phase from day 2 to day 12. The degradation phase is from 10% biodegradation until biodegradation reaches greater than 60% degradation. The pH of the solutions with the test and reference substances and the Inoculum control blank solutions on day 25 varied by 0.5 pH units or less from that on day 0 (see Table 3). The total CO2 evolution in the inoculum control blanks at the end of the test averaged 42.9 mg CO2, which is equivalent to 14.3 mg CO2/L (Table 2). The difference of extremes of replicate values of the test substance at the end of the test was less than 20% (Table 2). - Results with reference substance:
- Sodium benzoate (the reference substance) was greater than 60% biodegradable within 14 days confirming that the inoculum was viable.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test substance met the criteria for “Ready Biodegradable” under conditions of this test and was not inhibitory to microorganisms in the inoculum. The test was valid.
- Executive summary:
The test substance was tested for ready biodegradability using the 28-day CO2 Evolution test for “Ready Biodegradation” according to OECD Guideline 301B in the version dated July 17, 1992. This test is also known as the Modified Sturm Test. The biological system used was secondary activated sludge from the Elkton, Maryland (U.S.A) Publicly-Owned Treatment Works (POTW). The biodegradation process was monitored on days 1, 4, 6, 8, 12, 18 and 25 when carbon dioxide (CO2) trapped in barium hydroxide was measured by titration of the residual hydroxide. Additionally, traps were titrated on day 26 to quantify any remaining CO2 after acidifying the test systems on day 25. The amount of CO2 produced from the test substance (corrected for that from the Inoculum Control Blank) is expressed as a percentage of the total CO2 that the test substance could have theoretically produced (ThCO2) based on the measured total carbon (TC) content of the test substance.
Findings:
- the test substance reached a maximum biodegradability of 72.5 % by Day 26;
- greater than 60% biodegradability was reached by day 12 and was within 10 days of exceeding 10% biodegradation.
- the toxicity control, which included both the test substance and the reference substance in the same vessel, attained greater than 25% biodegradation within 14 days.
- the reference substance attained a biodegradation level of greater than 60% within 14 days.
Reference
Table 1. Descriptions of Inoculum Control Blank and Test and Reference Substances |
||
Substance Test Systems |
Initial Amount of Substance (mg) |
ThCO2 (mg THCO2/ mg substance) |
Inoculum Control Blank Rep 1 |
NA* |
NA |
Inoculum Control Blank Rep 2 |
NA |
NA |
Inoculum Control Blank Rep Avg |
NA |
NA |
Test Substance Rep 1 |
90.3 |
218 |
Test Substance Rep 2 |
91.6 |
221 |
Test Substance Avg |
90.95 |
219.5 |
Test Substance TOX |
91.1mg test substance +102.0 mg reference substance 102 mg Ref. sub. |
438 |
Reference Substance, Substance Benzoate |
102.9 |
220 |
*Not Applicable |
Table 2. Cumulative CO2 Production in the Inoculum Control Blank and Test Substance, Toxicity Control and Reference Substance Biodegradation |
||||
Days |
Inoculum Control Blank (mg CO2) |
Test Substance Avg Biodegradation(%) |
Toxicity Control (%) |
Reference Substance (%) |
0 |
0.0 |
0 |
0.0 |
0.0 |
1 |
2.9 |
1.9 |
2.2 |
0.4 |
4 |
17.9 |
40.5 |
32.4 |
49.5 |
6 |
19.8 |
45.2 |
37.7 |
54.7 |
8 |
23.5 |
50.3 |
43.6 |
59.6 |
12 |
28.7 |
62.2 |
54.2 |
68.6 |
18 |
35.2 |
64.9 |
55.5 |
70.1 |
25 |
42.0 |
68.4 |
58.0 |
72.5 |
26 |
42.9 |
72.5 |
60.6 |
75.9 |
Table 3. pH Values on Days 2 and 25 |
||||
Substance |
Day 0, Rep 1 |
Day 0, Rep 2 |
Day 2, Rep 1 |
Day 25, Rep 2 |
Test Substance |
7.07 |
7.09 |
6.80 |
6.81 |
Toxicity Control |
7.11 |
NA* |
6.93 |
NA |
Inoculum Control Blank |
7.18 |
7.13 |
7.02 |
6.94 |
Reference Substance |
7.12 |
NA* |
6.97 |
NA |
*Not Applicable – these two substances were not replicated. |
Description of key information
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
The test substance was found to fulfil the criteria for readily biodegradable in a GLP-compliant OECD 301B guideline test.
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