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EC number: 212-379-1 | CAS number: 812-00-0
- 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
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
- Study period:
- 27 February to 25 July 2018
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-D (Determination of the "Ready" Biodegradability - Manometric Respirometry Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Batch 34448
Purity 67.9 - 71.2 % Methyl dihyrdogen phosphate
Expiry 30 March 2022 - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- Activated sludge from a biologic sewage treatment plant was used. The chosen plant is treating mostly household sewage.
The sludge was taken from the activation basin of the sewage treatment plant in D-67480 Edenkoben.
Date of collection: 28. Feb. 2018
Batch no: 20180228.
The sludge was filtrated, washed with medium 2x, and re-suspended in test medium. It was then aerated. The dry matter was determined as 4520 mg suspended solids/L. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 264 mg/L
- Based on:
- test mat.
- Initial conc.:
- 100.06 mg/L
- Based on:
- ThOD
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- Preparation
The medium was prepared using the stock solutions. The dry matter of the inoculum was determined. A sufficient number of test vessels was provided. The stock solution the positive control was freshly prepared. The test item was pipetted directly into the test vessels. Before the start of the test, the cartridge of the measuring heads was filled with soda lime and the program parameters (duration of the test, volume of the test flasks and volume of the test solution) were selected.
Experimental Parameters
Test item concentration: 264 mg test item/L
ThOD concentration test item: 100.06 mg ThOD /L
Positive control concentration: 60 mg sodium benzoate/L (corresponding to 100.08 mg/L ThOD)
Number of control flasks: 3 (medium and inoculum)
Number of positive control flasks: 3 (sodium benzoate, medium and inoculum)
Number of test vessels: 3 (test item, medium and inoculum)
Abiotic control: 1 (test item and 10 mL 1% HgCl2 solution/L)
Toxicity control: 1 (200.14 mg/L ThOD)
Volume of test vessels: 500 mL (590 mL total volume including measuring head)
Volume test solution: 250 mL (toxicity flask 125 mL)
Concentration of suspended solids 25.0 mg/L
Temperature: 20.7 – 21.1 °C 21.4 – 22.2 °C (toxicity control)
Duration: 28 days
Start of the Test
The test vessels were filled with medium, then test item and positive control were added to the appropriate vessels and the pH was adjusted to 7.2 – 7.6. After pH-adjustment, the inoculum was added, the vessels were connected to the OxiTop® measuring heads and they were started via the OxiTop® Controllers.
Performance of the Test
The oxygen which was consumed by the content of the vessels was measured automatically by the test apparatus. After 28 days, the test was ended. Because the test item and positive control do not contain nitrogen, presence of nitrate and nitrite was not checked.
Calculation of Degradation
Oxygen Demand The oxygen demand of test item and positive control vessels and for each measuring point were calculated. - Reference substance:
- benzoic acid, sodium salt
- Test performance:
- All validity criteria were met. Oxygen consumption in the blank controls and in the positive controls was normal, indicating that the test system has worked properly. As a plateau of degradation was reached it is considerable, that the maximal degradation of the test item under the stated test conditions was reached. The ThOD of the test item was calculated based on a theoretical formula of the test item, calculated asC1H5.58O4.45P1. The formula was based on elemental analysis. The sum of analysed elements (9.50% C, 4.45% H, 26.7% P, 56.3%O) was 97 %.
No observations were made which might cause doubts concerning the validity of the study outcome. The result of the test can be considered valid. - Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 71
- Sampling time:
- 28 d
- Details on results:
- The degree of biodegradation reached 71 % after 28 days. Because the test item is a mixture the 10-day-window does not have to be taken into account. As degradation surpassed 60% in the course of the test, regardless of the 10-daya window Methyl dihydrogen phosphate is considered as readily biodegradable.
- Results with reference substance:
- 85% degradation over 28 days based on O2 consumption.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- Readily Biodegradable.
- Executive summary:
The degree of biodegradation reached 71 % after 28 days. Because the test item is a mixture the 10-day-window does not have to be taken into account. As degradation surpassed 60% in the course of the test, regardless of the 10-daya window Methyl dihydrogen phosphate is considered as readily biodegradable.
Reference
Description of key information
Readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Additional information
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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