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EC number: 205-187-4 | CAS number: 135-37-5
- 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 soil
Administrative data
Link to relevant study record(s)
Description of key information
Since no specific studies are available for EDG, in this section reference is made to the structurally comparable NTA, for which relevant information is available. For read across justification, please refer to section 13.
The overall conclusion from the studies is that Na3NTA can be quickly degraded under aerobic conditions in previously adapted soils. The degradation is limited under O2 deficient conditions and in non-adapted soils. A possible degradation intermediate of Na3NTA degradation in soils is iminodiacetate.
For EDG a similar biodegradation rate and pattern is expected.
Key value for chemical safety assessment
- Half-life in soil:
- 56 d
- at the temperature of:
- 25 °C
Additional information
Based on read across justification, only studies for NTA have been included, since no specific data for EDG are available. Studies relating to Na3NTA, nitrilotriacetic acid (NTA acid, H3NTA) and nitrilotriacetate are considered for the assessment of this endpoint.
The results obtained by Tabatabai & Bremner (1975) show that trisodium nitrilotriacetate monohydrate (Na3NTA * H2O) is readily decomposed by soil microorganisms under aerobic or anaerobic conditions (≥ 50 % degradation after 5 days of incubation at 30 °C). NTA-N was converted to nitrate and ammonium under aerobic and anaerobic conditions, respectively.
The results of the soil column studies conducted by Dunlap et al. (1971) also indicate rapid and complete biodegradation of Na3NTA under aerobic conditions. In contrast, the results Dunlap et al. (1971) with anaerobic sand, loam, and clay-loam soil columns clearly demonstrate slow and incomplete biodegradation of Na3NTA, indicating that Na3NTA infiltrating through saturated soil systems such as flooded septic tank percolation fields or under waste water lagoons, will likely undergo at most only slow degradation (half-lives were not reported).
Further study results are available for nitrilotriacetic acid (NTA acid, H3NTA) and nitrilotriacetate. NTA acid, Na3NTA, and nitrilotriacetate display the same behaviour in the environment: splitting of sodium ions or protons (in case of NTA and NTA acid) and uptake of multivalent metal ions with subsequent formation of 1:1 or 1:2 complexes.
Since sodium salts are generally considered to be completely dissociating, a solution of Na3NTA in water yields the tribasic anion nitrilotriacetate. Nitrilotriacetic acid is a weak acid, and in such a solution, the NTA will therefore exist as an equilibrium mixture of several species:
NTA- - -<-> HNTA- -<-> H2NTA-<-> H3NTA <-> H4NTA+
with the last species occurring when, in a very acidic environment, the central nitrogen atom is protonated.
Due to pH differences, the NTA speciation equilibrium will be different for Na3NTA and for NTA acid, unless dissolved in a buffered solution (controlled pH). A solution of NTA acid will be (slightly) acidic, whereas a Na3NTA solution will be alkaline (‘basic’). Toxicologically, this is not assumed to be significant, since it can be presumed that ‘in vivo’ systems are buffered systems. The chelating behaviour of Na3NTA and NTA acid will be slightly different, but this is not a significant effect for the relevant endpoint under REACH with regard to environmental fate and behaviour, ecotoxicology and toxicology.
Therefore, also results on NTA acid and nitrilotriacetate are considered for the assessment of trisodium nitrilotriacetate using read-across. This is in line with the Canadian ‘Draft Screening Assessment for Nitrilotriacetic acid (CAS 139-13-9)’ from January 2010,which also considered information relating to Na3NTA and nitrilotriacetate in the assessment of NTA acid. This is due to the fact that the toxicological endpoints, as stated in the Canadian ‘Screening Assessment for Nitrilotriacetic acid’, of NTA acid and Na3NTA are similar. Moreover, the dissociation of NTA acid and Na3NTA leads to the common moiety nitrilotriacetate.
Data from studies with salts formed with various cations such as calcium, magnesium, aluminum, zinc and iron were not included. Canada and the European Union also similarly did not include these other NTA salts in the ‘Draft Screening Assessment for Nitrilotriacetic acid’ and the ‘Draft Risk Assessment Report (EURAR 2008)’, respectively.
One additional study was conducted by Tiedje & Mason (1974). In contrast to the findings of Tabatabai and Bremner (1975), results from Tiedje & Mason (1974) indicate that14CO2production from nitrilotriacetate (NTA) did not occur anaerobically and was severely limited under microaerophilic conditions. This finding is in line with the results obtained by Dunlap et al. (1971). In accordance with Tabatabai & Bremner (1975) and Dunlap et al. (1971), Tiedje & Mason (1974) found rapid degradation of NTA under aerobic conditions, with iminodiacetate as possible degradation intermediate.
Besides, the results of Tiedje & Mason (1974) show that NTA degradation rates did not correlate with pH, drainage, texture, or plant cover. Rates of degradation increased with increasing substance concentrations. NTA was found to be degraded also at low temperatures (2 °C) in previously acclimatized soils. At room temperature degradation rates were highest in soils receiving sewage effluent and in muck soils (at 40 ppm NTA: 8 to 10 ppm/day which is equivalent to 0.2 to 0.25 d-1and half-lives of 2.8 to 3.5 days) while the degradation in mineral surface soils ranges from 0.5 to 6 ppm/day (at 40 ppm NTA; equivalent to 0.0125 to 0.15 d-1and half-lives of 4.6 to 55.5 days).
The assumption that adaption seems to be key process is further supported by the results determined by Shimp et al. (1994), as illustrated by the rapid biodegradation of nitrilotriacetic acid (NTA acid) near the tile field (half-lives ≥ 1 - ≤ 3 days in soils and sediment samples, and ≤ 1 day in groundwater samples) and limited biodegradation at locations far downgradient or ungradient of the system, where little or no NTA acid loading occurred (half-life of approximately 1.7 days for groundwater samples in 60 m distance from the tile field, almost no biodegradative activity in soil samples collected from sites 20m downgradient form the tile field).
From these studies it can be concluded that Na3NTA can be readily degraded under aerobic conditions in previously adapted soils. The degradation is limited under O2 deficient conditions and in non-adapted soils. As reported half-lives in non-adapted soils range between 4.6 and 55.5 days, NTA cannot be regarded as persistent in soils.
For aerobic mineralisation of Na3NTA, half-lives between 1 and 56 days were determined. For the exposure calculations, a half-life of 56 days is used as a worst case.
For EDG a similar biodegradation rate and pattern is expected.
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