Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 203-929-1 | CAS number: 112-03-8
- 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
Toxicity to terrestrial arthropods
Administrative data
- Endpoint:
- toxicity to terrestrial arthropods: long-term
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Biodegradation in water:
- readily biodegradable
- Type of water:
- freshwater
Based on the available weight of evidence, the test substance can be considered to be readily biodegradable undergoing complete mineralisation.
Study 1: A study was conducted to determine the biodegradation in water of the test substance, C18 TMAC (99.5% active) according to OECD guideline 301D, EU Method C.6 and ISO 10707 (Closed Bottle test), in compliance with GLP. The test was performed with activated sludge, domestic in 0.30L BOD (biological oxygen demand) bottles with glass stoppers. There were 10 bottles containing only river water, 6 bottles containing river water and sodium acetate, 10 bottles containing river water with the test substance. The concentrations of the test substance, and sodium acetate in the bottles were 1.0, and 6.7 mg/L, respectively. (A slight inhibition of the endogenous respiration of the inoculum by the test substance was detected at day 7. Therefore, limited inhibition of the biodegradation due to the "high" initial concentration of the test compound is expected. This toxicity was the reason for testing at an initial test compound concentration of 1.0 mg/L). The test substance was biodegraded by 77% at Day 28 in the Closed Bottle test. The test was valid, as shown by an endogenous respiration of 1.1 mg/L and by the total mineralization of the reference compound, sodium acetate. Sodium acetate was degraded by 66% of its theoretical oxygen demand after 14 day. Oxygen concentrations remained >0.5 mg/ L in all bottles during the test period. Under the study conditions, the test substance can be considered readily biodegradable, but failing 10 -day window (van Ginkel, 2005).
Study 2: A study was conducted to determine the biodegradation of the test substance, C18 TMAC (80% active) in water according to OECD Guideline 301D (closed bottle test), in compliance with GLP. Non-adapted activated sludge was exposed to 3 mg/L test substance (corresponding to 2.4 mg a.i./L based on a purity of ca. 80%), equivalent to a theoretical oxygen demand of 6.96 mg O2/L, for 28 days. A reference substance and a toxicity control were run in parallel. The test substance degraded to 18% within 28 days. Degradation of the reference substance and the toxicity control were 86 and 67%, respectively. Under the study conditions, the test substance was not readily biodegradable (Noack, 1997).
Study 3: A study was conducted to determine the biodegradation of the test substance, C18 TMAC (49% active in hydroalcoholic solution) in water according to OECD Guideline 301D (closed bottle test), in compliance with GLP. The test was performed with activated sludge, domestic and non-adapted, exposed to 4.0 mg/L test substance (49% active substance and 36% 2-propanol) for 35 days. Silica gel was added in the study setup to reduce the concentration of test substance in the water phase, thereby reducing its toxicity. The test substance in the presence of silica gel caused no reduction in the endogenous respiration. In the presence of silica gel, test substance was biodegraded 48% at day 28. In the prolonged closed bottle test with silica gel the biodegradation percentage reached 53% at day 35. Hence, test substance should be classified as biodegradable.The test is valid as shown by an endogenous respiration of 0.95 mg/I and by the total mineralization of the reference compound, sodium acetate. Sodium acetate was degraded 77% of its theoretical oxygen demand after 14 days. Finally, the most important criterion was met by oxygen concentrations >0.5 mg/I in all bottles during the test period. Due to the large fraction of 2-propanol in the test substance (approximately 36%) it could not be concluded that the active test substance was biodegradable. Under the study conditons, the test substance was determined to be inherently biodegradable (van Ginkel, 1993).
Study 4: A study was conducted to determine the biodegradation of the test substance, C18 TMAC (Purity: 92%) in water according to OECD Guideline 301D (closed bottle test), in compliance with GLP. The test was performed with activated sludge, domestic and non-adapted, exposed to 2.0 mg/L test substance (92% purity) for 175 days. The test was realised with and without silica gel. In the prolonged closed bottle test without silica gel, the substance degraded up to 77% by Day 175. Toxicity of test substance results in a long lag phase of 55d. After 55d biodegradation starts and reaches 77% at Day 175 showing complete minteralization of test substance. In the test with silica gel, (added to ensure a slow release of the test substance into the water phase), the substance was 30% biodegraded at Day 28 and reached 57% biodegradation at Day 84. In this test the lag phase is reduced to 5d. The test substance has to desorp from the silica gel into the water phase to be bioavailable for the micro-organisms. Desorption and herewith bioavailability of test substance is probably the liming factor in the experiment with silica, resulting in a biodegradation percentage that levels just around the 60%. Both tests were valid as shown by endogenous respirations of 0.4 and 0.5 mg/L and the total mineralization of the reference substance, sodium acetate. Under the study conditions, the test substance was considered to be inherently biodegradable (van Ginkel, 1990).
In general, the use of silica gel in biodegradation studies is supported by the findings from van Ginkel 2008, which showed that silica gel was the best adsorbent as compared to lignosulphonic acid and humic acid see Figure 1 in CSR.
In addition, recent publications from Timmeret al., 2019 and Nabeokaet al., 2020 indicate that use of appropriate concentrations of moderate adsorbent carriers like silica gel has the ability to reduce the microbial toxicity of quaternary ammonium substances (by lowering their concentrations) and hence increasing their biodegradation. However, the use of silica gel was found to have no effect on highly persistent substances with specific chemical structures, e.g., branched alkyl chain containing substances as in benzethonium chloride (Nabeokaet al., 2020). This is a critical observation as it demonstrates that use of silica gel in the studies with the linear alkyl chain containing quaternary substances like the test substance does not overestimate the biodegradation.
Further, the results obtained with the test substance are in agreement with what is reported in the literature for other quaternary ammonium substances, as summarized below inTable 4.4.
Table 4.4. Compilation of ready biodegradability test results obtained with quaternary ammonium salts (adapted van Ginkel, 2007)
Substance |
Test |
Results at Day 28 (%) |
Octadecyltrimethylammonium Chloride (C18 TMAC) |
Sturm test |
>70 |
Hexadecyltrimethylammonium Chloride (C16 TMAC) |
Headspace Carbon Dioxide |
75* |
Cocotrimethylammonium (Coco TMAC) |
Closed bottle |
>60 |
Octylbenzyldimethylammonium chloride (C18 ADBAC) |
MITI |
>80 |
Tetradecylbenzyldimethylammonium Chloride (C14 ADBAC) |
MITI |
>80 |
Decylbenzyldimethylammonium Chloride (C10 ADBAC) |
Closed bottle |
>60 |
*Mean from 10 laboratories; also cited in OECD TG 310 (adopted on 23 March 2006)
In addition, several literature data are available to clarify the metabolic basis of degradation by micro-organisms. Bacteria identified asPseudomonas spcapable of degrading alkyltrimethylammonium salts were isolated from activated sludge (van Ginkelet al., 1992; Takenakaet al., 2007). Alkyltrimethylammonium salts with octadecyl, hexadecyl, tetradecyl, dodecyl, decyl, octyl, hexyl and coco alkyl chains supported growth of the isolates, showing the broad substrate specificity with respect to the alkyl chain length. Alkanals, and fatty acids can also serve as a carbon and energy source (van Ginkelet al., 1992; Takenakaet al., 2007). In simultaneous adaptation studies,1H nuclear magnetic resonance spectrometry (1H-NMR) and GC-MS showed that acetate, alkanals and alkanoates are the main intermediates of alkyltrimethylammmonium salt degradation, indicating that the long alkyl chain is utilized for microbial growth (van Ginkelet al., 1992; Nishiyama and Nishihara, 2002; Takenakaet al., 2007). Trimethylamine is stoichiometrically produced by pure cultures of microorganisms growing with the alkyl chain of alkyltrimethylammonium chloride as the sole source of carbon. The cleavage of the C-alkyl-N bond of alkyltrimethylammonium salts resulting in the formation of trimethylamine is initiated by a mono-oxygenase (van Ginkelet al., 1992). Additional evidence of the cleavage of the C-alkyl-N bond as the initial degradation step of alkyltrimethylammonium salts was presented by Nishiyamaet al. (1995) and Takenakaet al. (2007).
Dehydrogenase activity present in cell-free extract of hexadecyltrimethylammonium chloride-grown cells catalysed the oxidation of alkanal to fatty acids. The route of the fatty acid degradation is by β-oxidation. Trimethylamine, a naturally occurring compound is readily biodegradable (Pitter and Chudoba 1990). Complete degradation of trimethylamine is demonstrated through the assessment of the biodegradation pathway. Trimethylamine is degraded by methylotrophic bacteria through successive cleavage of the methyl groups (Large, 1971; Meiberg and Harder, 1978). Consortia of microorganisms degrading the alkyl chain of alkyltrimethylammonium salts and trimethylamine are therefore capable of complete (ultimate) degradation of alkyltrimethylammonium salts. Complete degradation of alkyltrimethylammonium salts using a mixed culture has been demonstrated by Nishiyamaet al.(1995). More recently, Nishiyama and Nishihara (2002) have isolated aPseudomonas sp. capable of degrading both the alkyl chain and trimethylamine. Both the pure and mixed culture studies showed that the degradation of the alkyl chain of alkyltrimethylammonium salts results in the formation of water, carbon dioxide and ammonium (seeFigure 2).
Figure 2: Biodegradation pathway of alkyltrimethylammonium salts (van Ginkel, 2004, 2007)
Further, according to the evidence presently available on the biodegradation rate, microorganisms readily oxidize the hydrophobic alkyl chains of the cationic surfactants, which is followed by a slower oxidation of the hydrophilic moiety (the corresponding amines) (van Ginkel, 2004). The above biodegradation process for the two moieties plays a key role in the differences in the results between the different cationic surfactants. However, based on the available experimental data and literature evidence, the alkyl chains and the trimethylamine of the test substance is readily biodegradable.
Overall, considering all the above information together, the test substance is considered to be readily biodegradable undergoing complete mineralization.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Half-life in soil:
- 17.1 d
- at the temperature of:
- 12 °C
Based on the most recent and radiolabelled aerobic biodegradation study in soil with the read across substance, C12-16 ADBAC, the transformation of the substance was considered to be rapid with DT50 values ranging from 2.2-28.7 days with the SFO model and 1.6 – 23.3 days with the FOMC model at 20°C. Further, in the biocides dossier, a weighted estimate of the DT50 value at 12°C was extrapolated for C12-16 ADBAC by assuming the highest allowable concentrations for the major chains. These calculations resulted in the estimated FOMC DT50 of 17.1 days at 12°C and SOF DT50 of 19.2 days at 12°C. The DT50 of 17.1 days at 12°C based on the biphasic model (FOMC) showing better visual fit and lower error (x2)compared to the SFO model was used further for risk assessment.
Study 1: A study was conducted to determine the aerobic transformation/dissipation in the soil of the read across substance, C12 -16 ADBAC (radiochemical purity: 98.5%), according to the OECD Guideline 307, in compliance with GLP. Four different standard soils (LUFA 2.2, 2.3, 2.4 and 5M, field fresh sampled), varying in their organic carbon content, pH, clay content, cation exchange capacity and microbial biomass, were treated with [ring-U-14C] Benzalkonium chloride. Soil samples were incubated in the dark under aerobic conditions for up to 128 days under controlled laboratory conditions. After appropriate time intervals, soil samples were extracted, and the extracts were analysed for read across substance and transformation products to calculate DT50 and DT90 values. The mineralization was determined by trapping and analysis of the evolved 14CO2. Non-extractable residues (NER) were determined after combustion of the extracted soil samples. The total radioactivity of the soil extracts, the extracted soil (NER) and evolved 14CO2 was determined by LSC. Read across substance and transformation products in the soil extracts were analysed by LC-FSA (radio-HPLC). Evaluation of the transformation pathway was done by LC-HRMS. Transformation of the C12 chain of the read across substance [ring-U-14C]Benzalkonium chloride was rapid in all four soils. The transformation of the C14 chain started after a short adaptation phase but was thereafter rapid as well. Within 7 - 21 days the concentration of the C12 chain decreased from initially 67.2 – 69.6% of applied radioactivity (AR) to < 20 % of AR. The concentration of the C14 chain decreased from initially 23.8 – 24.6 % of AR to < 10 % of AR within 10 – 36 days. Formation of NER started directly after application of the read across substance. Further formation of NER increased in parallel to the start of increased mineralisation, indicating that a major amount of NER is comprised by radioactivity incorporated in microbial biomass. At the test end, the biomass concentration was in the range of 1.46 – 2.62 % of soil organic carbon content in all four soils, indicating that viable microbial biomass was present throughout the incubation time. The mass balance was in the range 99.9 – 103.0 % at test start and 90.4 – 94.0 % at test end.The predominant initial degradation step was the oxidative removal of the alkyl chain. Dimethylbenzylamine was determined as the major metabolite, the highest concentrations of dimethylbenzylamine were determined until Day 22, thereafter the concentrations deceased continuously until test end. Methylbenzylamine was transient and only present in traces. Benzylamine, a suspected metabolite, was not detected. Further metabolites containing partly degraded alkyl chains were all transient and were not detected or only <0.2 % of AR (soil 2.3) at the test end. With regard to the kinetics, the transformation showed a slight bi-phasic pattern, therefore the ‘Single First Order Model’ (SFO) and the ‘First-Order Multi-Compartment Model’ (FOMC) were compared. Based on the visual fit and x2 error, the transformation of [ring-U-14C]Benzalkonium chloride met the requirements for both models well for all four soils. The calculated DT50 values with the Single-First-Order Model (SFO) for the dissipation of [ring-U-14C]Benzalkonium chloride were 2.2 – 8.7 days (C12 chain) and 6.1 – 28.7 days (C14 chain), the DT90 values were 7.2 – 28.8 (C12 chain) days and 20.2 – 95.4 days (C14 chain). The calculated DT50 values with the FOMC model for the dissipation of [ring-U-14C]Benzalkonium chloride were 1.6 – 7.2 days (C12 chain) and 5.5 – 23.3 days (C14 chain), the DT90 values were 15.0 – 48.8 days (C12 chain) and 35.8 – 164.3 days (C14 chain).
The read across substance is predominantly C12-ADBAC and C14-ADBAC, with low to negligible amounts of C16-ADBAC. The chain length distribution is defined as follows:C12 (35-80%), C14 (20-55%), C16 (0-15%). C16-ADBAC was not included in this study because it is present in very low amounts; there are technical difficulties with having sufficient radioactivity for substances present in small amounts relative to other constituents. C16-ADBAC would be expected to degrade by the same route but at a slower rate than its C12 and C14 counterparts, as degradation rate tends to decrease with increasing chain lengths.Under the study conditions, transformations of both C12 and C14 carbon chains of the read across substance were determined to be rapid in all four soils and the DT50 values were determined to be 2.2 – 8.7 days [C12 chain] and 6.1 – 28.7 days [C14 chain] with the SFO model and 1.6 – 7.2 days [C12 chain] and 5.5 – 23.3 days [C14 chain] with the FOMC modelat 20°C (Fiebig, 2019).
Further, in the biocides dossier, to account for the potential contribution of C16 ADBAC to the overall DT50 of ADBAC, a geometric mean of SFO and FOMC DT50s for C12 and C14 ADBAC in the four soils (as recommended in BPR Vol IV Part B and C) was calculated and converted to 12° using the following equation (DT50 (12°) = DT50 (20°) * e(0.08*(20-12)). This was followed by linear extrapolation of the geometric mean DT50s for C12 and C14 ADBAC, to estimate the DT50 for C16 ADBAC. See table below:
|
Soil 2.2 |
Soil 2.3 |
Soil 2.4 |
Soil 5M |
Geo. Mean |
Adj. to 12° C |
SFO DT50s |
||||||
C12 ADBAC |
2.2 |
3.3 |
6.2 |
8.7 |
4.4 |
8.4 |
C14 ADBAC |
6.1 |
8.9 |
12.9 |
28.7 |
11.9 |
22.6 |
C16 ADBAC |
-- |
-- |
-- |
-- |
-- |
36.7 |
FOMC DT50s |
||||||
C12 ADBAC |
1.6 |
3.2 |
5.8 |
7.2 |
3.8 |
7.3 |
C14 ADBAC |
5.5 |
8.3 |
12.1 |
23.3 |
10.7 |
20.2 |
C16 ADBAC |
-- |
-- |
-- |
-- |
-- |
33.1 |
A weighted estimate of the DT50 of ADBAC (C12-C16) at 12°C was calculated by assuming the highest allowable concentrations of C14- and C16- ADBAC and the balance of C12-ADBAC (i.e., 12% C16, 52% C14 and 36% C12), which resulted in the following estimated DT50s:
SFO DT50 = 19.2d at 12°C; FOMC DT50 = 17.1d at 12°C
However, due to the relatively low levels of C16-ADBAC, the overall estimated DT50s were considered rather insensitive to the assumed DT50 for C16-ADBAC.The DT50 of 17.1 days at 12°C based on the biphasic model (FOMC) showing better visual fit and lower errorwas used further for risk assessment.
Based on the results of the read across study, similar degradation potential and half-life is considered for the test substance.
Study 2:A study was conducted to determine the aerobic biodegradation of the read across substance, C12-16 ADBAC (50% active in water) in loamy soil, according to the US FDA Environmental Assessment Handbook, Technical Assistance Document 3.12 (1987). The study comprised two treatments: test and chemical blank control group, each with three replicates. The read across substance was added into biometers at a concentration of 10 mg carbon per 50 g soil using appropriate amount of deionised water required for bringing the soils to 50-70% of the moisture capacity. Loam was added to the biometers after the test solutions to facilitate uniform moistening of the soils by capillary action. The test was then incubated at 22 ± 3°C and run for approximately 90 d. The side tube of the biometer contained 20 mL 0.2 M KOH for absorbing carbon dioxide produced by the microorganisms. The theoretical CO2 production of the read across substance was calculated from its carbon content. The amounts of carbon dioxide were calculated by subtracting the mean carbon dioxide production in the test systems containing the read across substance and the mean carbon dioxide production level in the control blank. Biodegradation was calculated as the ratio of experimental carbon dioxide production to theoretical carbon dioxide production [ThCO2P]. Under the study conditions, there was 64% degradation of the read across substance after 70 days. This percentage of the theoretical carbon dioxide production presumes complete mineralization. The DT50 was estimated to be 40 days (Ginkel, 1994). Based on the results of the read across study, similar degradation potential and half-life is considered for the test substance.
Based on the most recent and radiolabelled aerobic biodegradation study in soil with the read across substance, C12-16 ADBAC, the transformation of the C12 and C14 carbon chains of the substance was considered to be rapid with DT50 values ranging from 2.2-28.7 days with the SFO model and 1.6 – 23.3 days with the FOMC model at 20°C. Further, in the biocides dossier, a weighted estimate of the DT50 value at 12°C was extrapolated for C12-16 ADBAC by assuming the highest allowable concentrations for the major chains. These calculations resulted in the estimated FOMC DT50 of 17.1 days at 12°C and SOF DT50 of 19.2 days at 12°C. The DT50 of 17.1 days at 12°C based on the biphasic model (FOMC) showing better visual fit and lower error (x2)compared to the SFO model was used further for risk assessment. Therefore, in line with the biocides dossier, the DT50 of 17.1 days at 12°C derived for the read across substance based on the biphasic model (FOMC) also has been considered further for hazard/risk assessment of the test substance.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- BCF (aquatic species):
- 79 L/kg ww
- BMF in fish (dimensionless):
- 0.046
The results of the read across study, supported with the estimated BCF value for the test substance together with its ionic nature indicates a low bioaccumulation and biomagnification potential. The higher experimental BCF value of 79 L/kg wt-wt from the read across study with C12-16 ADBAC and the growth corrected kinetic biomagnification factor (BMFkg) value of 0.0463 based on study with C18 TMAC, has been considered further for hazard/risk assessment.
Study 1:A study was conducted to determine the biomagnification of the test substance, C18 TMAC (purity 95%), following the principles of OECD TG 305. For the main study rainbow trout with an average weight of 5.42 g were fed per treatment test diets enriched with test substance (23.6 mg/kg test substance in feed). The resulting treatment and one control group (each 40 animals) were tested simultaneously. The uptake phase of 14 days was followed by a depuration phase lasting 14 days. All animals were fed the non-spiked feed during the depuration phase. The concentrations of the test substances in fish samples were determined by chemical analysis and all tissue concentrations were calculated based on a wet weight basis. Chemical analysis of the test substances was performed by liquid chromatography with coupled mass spectrometry (LC-MS/MS). In the main study five animals of each group were sampled randomized on day 7 and day 14 of the uptake phase and after 10 h, 24 h, 2 days, 3 days, 7 days and 14 days of depuration. Biomagnification factor (BMF) and distribution factor were calculated based on the tissue concentrations measured at the end of the uptake phase. No mortality or abnormal behaviour of the test animals were observed during the main study. The experimental diets were accepted by the test animals and showed a decent digestibility as confirmed by the texture and appearance of the feces. One fish was euthanized at day 25 due to injuries. The specific growth rates of the animals ranged from 1.95 to 2.71 %/d over the entire experiment. During the study, the feed conversion ratio (FCR) was 0.69 to 0.95. Fish were measured and weighed at the beginning of the experiment as well as at respective sampling time points to monitor growth and associated growth-dilution effects during the feeding study. Growth rate constants were determined separately for the uptake and depuration phases, for the treatments and the control group, using the ln-transformed weights of the fish. A subsequent parallel line analysis (PLA, as suggested by the OECD Guideline) resulted in no statistical differences between the uptake and the depuration phase among the treated groups with test substance. No statistically significant difference was detected with regard to the growth of the treated groups. Hence it was deduced that neither adverse nor toxic effects were caused by the enriched diets. As steady state seemed to be reached after 14 days of exposure, steady state biomagnification factors (BMFss) could be calculated as 0.02709 g/g, which showed that test substance did not biomagnify after dietary exposure. In general, the GIT and the liver showed the highest values for the BMFk and BMFkg. The kinetic BMF (BMFk) and growth-corrected biomagnification factor (BMFkg) were calculated for the test substance to be 0.0404 and 0.0463, respectively. Overall, it was concluded from the screening that ionization lowers the tendency of a chemical to bioaccumulate, compared to non-ionized chemicals. Aside of the well-known lipophobicity of ionized groups, fast depuration seems to be a major reason for the observed low biomagnification of ionic compounds, in particular anions. Fast depuration may happen due to rapid metabolism or conjugation of charged compounds, and future studies should test this hypothesis. Under the study conditions, the test substance BMFss, BMFk and BMFkg values on whole body wet weight basis in rainbow trout were determined to be 0.02709, 0.0404 and 0.0463 g/g, respectively (Schlechtriem, 2021).
Study 2: A study was conducted to determine the tissue distribution of two cationic surfactants mixtures in Rainbow Trout (Oncorhynchus mykiss) following exposure via water for seven days and analysis of different fish tissues. The test chemicals were grouped into two mixtures of six containing 10 alkyl amines and 2 quaternary alkylammonium surfactants: C10 TMAB (as part of MIX 2) and C14 TMAC (as part of MIX 1). Studying chemical mixtures has the advantage that differences in behavior between chemicals are not obscured by biological variability or experimental variables. Bioconcentration studies with mixtures have been shown to provide similar results to studies with single chemicals. The experiments were conducted in 300 L fiberglass aquaria with a water renewal rate of 1.3 L min−1 (MIX 1) and 1.45 L min−1 (MIX 2). A solution of the test chemical mixture in methanol was infused continuously (3.5 and 3.8 μL min−1 for MIX 1 and MIX 2, respectively) into the water inflow using a syringe pump. The intended concentrations of C10 TMAB and C14 TMAC were 59 and 1.3 μg/L (measured). The water temperature was 10 °C and the pH 7.5. The water hardness was estimated to be 1.1 mM Ca2+. For each mixture, the syringe pump was started in an aquarium containing no fish. After 16 h, to allow the concentrations to stabilize, 12 rainbow trout were added. After 7 d of exposure, the fish in the exposure aquaria as well as several unexposed (control) fish were sacrificed followed by blood collection.The surface of the fish posterior of the gills was rinsed with 100% methanol to remove read across substance residues adsorbed to the outer surface of the skin and absorbed in the skin mucus.The fish were then dissected and the liver, the kidney, the gills, and the remaining contents of the abdominal cavity were taken and weighed. Skin and muscle samples were prepared from the upper dorsal region on semi-frozen fish after the methanol rinse had removed the mucus. For 6 fish from each aquarium and 3 control fish, samples of muscle, skin, liver, and gills were homogenized in a bullet blender (muscle and liver) or in a cryo-mill (skin and gill). A sub-sample of 0.5−1.2 g of the homogenate was extracted twice in methanol, employing centrifugation at 4000 rpm for phase separation. Isotope labeled standards of C10 TMAB and C14 TMAC were added to a portion of the extract corresponding to 12−75 mg of the sample. Whole blood was analyzed rather than plasma because of the small quantity of sample available and the anticipated low concentrations. The test chemical concentrations generally increased in the order muscle <blood < skin < gills < liver. Because the mass of extracted mucus was not determined, the concentrations in mucus were normalized to the estimated fish’s total surface area excluding the head, which was not rinsed. The concentration in mucus was on average 3.9 (range 0.9−11.6) times lower than the surface area-normalized concentration in gills. To calculate the quantity of the test chemical in the different tissues, the amount of each tissue in the fish was estimated and multiplied by the concentration in that tissue. The test chemical quantities in the different tissues were then summed to give the body burden in each fish. The apparent BCFs (BCFapp) values at the end of the 7-day exposure were calculated by dividing the surfactant body burden (blood, muscles, liver, gills, skin, mucus) by the fish mass, and dividing this by the average measured concentration in water samples taken during the exposure phase. Under the study conditions, the BCFapp for the two quaternary substances C10 TMAB and C14 TMAC were determined to be 0.1 and 31 L/kg ww, respectively. Mucus, skin, gills, liver, and muscle each contributed at least 10% of body burden for the majority of the test chemicals. In contrast to the analogue alkylamine bases, the permanently charged quaternary ammonium compounds accumulated mostly in the gills and were nearly absent in internal tissues, indicating that systemic uptake of the charged form of cationic surfactants is very slow (Kierkegaard, 2020).
Study 3:A study was conducted to determine the aquatic bioaccumulation of the read across substance, C12-16 ADBAC (30.64% active; 98.9% radiolabeled purity) in Lepomis macrochirus (bluegill fish) under flow-through conditions, according to EPA OPP 165-4, in compliance with GLP. The blue gill fish were continuously exposed to a nominal concentration of 0.050 mg/L of the read across substance (equivalent to a measured concentration of 0.076 mg/L) in well water for 35 days, followed by transfer of 35 fish into flowing uncontaminated water for a 21-d depuration period. Sampling was carried out on Days 0, 1, 3, 7, 9, 10, 14, 21, 23, 28 and 35 for the exposure period and Days 1, 3, 7, 10, 14 and 21 for the depuration period. Water samples were collected on Day 8 of the exposure period and Day 16 of the depuration for analytic determination of the read across substance concentration. Radiometric analyses of the water and selected fish tissues revealed that the mean steady state bioconcentration factor (BCF) in the edible, non-edible and whole-body fish tissue during the 35 days of exposure to be 33, 160 and 79 L/kg. The half-life for non-edible tissue was attained between Days 14 and 21, while it could not be reached for the edible and whole-body fish tissues by the end of 21-d depuration period. By Day 21 of the depuration period, the 14C residues present on the last day of exposure in the edible, non-edible and whole-body fish tissues had been eliminated by 29, 60 and 44% respectively. Analysis of skin tissue after 35 d of exposure showed residue levels somewhat higher than those observed for edible tissue at the same sampling period, indicating that there is likely significant binding of 14C-ADBAC to the skins and scales of exposed bluegill, as expected behaviour of cationic surfactants. Under the conditions of the study, the whole body BCF of the read across substance was determined to be 79, indicating low potential to bioaccumulate (Fackler, 1989).
Study 4:The Bioconcentration factor (BCF) value of test substance, C18 TMAC was predicted using regression-based and Arnot-Gobas BAF-BCF models of BCFBAF v3.02 program (EPI SuiteTMv4.11). The Arnot-Gobas method, takes into account mitigating factors, like growth dilution and metabolic biotransformations, therefore the BCF values using this method is considered to be more realistic or accurate. Therefore, except for ionic, pigments and dyes, perfluorinated substances, for which it is not recommended (as of now), the Arnot-Gobas method is used preferentially used for BCF predictions. Considering that test substance is a mono-constituent containing only ionic main constituents and impurities (e.g., the quaternary ammonium salts), the BCF values were predicted using regression-based model and using SMILES codes as the input parameter. The BCF values for the main constituent and the impurity were both predicted to be 70.80 L/kg ww (log BCF: 1.85), indicating a low bioaccumulation potential. On comparing with domain descriptors, both the constituent and the impurities were found to meet the MW, log Kow and/or maximum number of correction factor instances domain criteria as defined in the BCFBAF user guide of EPISuite. Overall, considering the BCF predictions for all the components, the test substance is expected to have a low bioaccumulation potential. However, taking into consideration the model’s training set and validation set statistics and the fact that the training set only contains 61 ionic compounds, the BCF predictions for the individual constituents are considered to be reliable with moderate confidence.
This is further supported by the no bioaccumulation potential evidence observed in in the two toxicokinetic studies in mammals with the read across substance, C12 -16 ADBAC (Selim, 1987 and Appelqvist, 2006). .
Also, the biocides assessment reports available from RMS Italy on Coco TMAC and C12-16 ADBAC, concluded the substances to show low potential for bioaccumulation, based on the results from the above study (Fackler, 1989) and an additional read across to DDAC for the Coco TMAC’s assessment ((ECHA biocides assessment report, 2015, 2016). The report concluded the following in the Coco TMAC assessment report:“Coco alkyltrimethylammonium chloride is readily biodegradable, is rapidly excreted and does not accumulate in mammals, and it adsorbs onto the fish surface where its irritating action is expressed (therefore accumulation is more related to the concentration of the administered solution). Based on these properties’ bioaccumulation is not expected to be of concern for ATMAC/TMAC. An experimental BCFwhole body of 81 L/kg was determined in a flow-through test with Lepomis machrochirus and the read across substance DDAC (Lonza Cologne GmbH and Akzo Nobel Surface Chemistry AB, same study). A very similar result was obtained for the other quaternary ammonium compound benzyl-C12-16-alkyldimethyl ammonium chloride (C12-16-BKC/ADBAC) in a fish bioconcentration test, which gave a BCFwhole body = 79 L/kg (Akzo Nobel Surface Chemistry AB, access to Lonza Cologne GmbH study). Being both studies equally reliable, the BCFwhole body = 81 L/kg is chosen because related to the lead read across substance (DDAC) and it is slightly higher than the C12-16 BKC/ADBAC endpoint.”
Overall, the results of the read across study, supported with the estimated BCF value for the test substance together with its ionic nature indicates a low bioaccumulation and biomagnification potential. The higher experimental BCF value of 79 L/kg wt-wt from the read across study with C12-16 ADBAC and the growth corrected kinetic biomagnification factor (BMFkg) value of 0.0463 based on study with C18 TMAC, has been considered further for hazard/risk assessment.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Short-term EC50 or LC50 for terrestrial plants:
- 277 mg/kg soil dw
- Long-term EC10, LC10 or NOEC for terrestrial plants:
- 856 mg/kg soil dw
In line with the C12-16 ADBAC biocides assessment report and based on the results of the read across study, the 16-d EC50 value of 277 mg a.i./kg dw of soil obtained forBrassica alba(mustard) due to effects on growth has been considered further for hazard/risk assessment. Additionally, in accordance with the ECHA R.7c guidance (2017), the 16-d NOEC value of 856.2 mg a.i./kg dw of soil obtained forTrifolium pratense(red clover) due to effects on growth can be considered as the long-term equivalent value.
Study 1:A study was conducted to determine the toxicity of the read across substance, C12-16 ADBAC (49.9% active in water) to terrestrial plants, according to OECD Guideline 208, in compliance with GLP. Three plant species:Sinapis alba(mustard),Trifolium pratense(red clover) andTriticum aestivum(wheat) were used. Using 0.5 L capacity plastic pots, the read across substance was first applied to natural soil at nominal concentrations of 0, 476.6, 856.2, 1540.9, 2772.2 and 4990.0 mg a.i./kg and to sand at nominal concentrations of 0, 28.8, 55.8, 93.4, 166.8 and 300.5 mg a.i./kg. This was followed by planting of 40 seeds per replicate of the three plant species. Analytical verification was performed for the read across substance. Three parameters: emergence, dry and wet weight of the plants were observed. Emergence was recorded daily until stabilisation. The plants in natural soil and sand were harvested 16 and 14 d respectively after 50% of the control seeds had been emerged. Wet and dry weight were determined immediately after harvesting. The test was considered as valid on the basis of percent emergence and further growth of the plant in the water control. The extraction of the active substance proved that the natural soil had a strong sorbing effect and the total recovery was not achieved even when acidified methanol was used as an extraction solvent. That was not the case with quartz sand. The LC50 values in natural soil based on effect on emergence were 3881, >4990 and >4990 mg a.i./kg dw of soil for mustard, red clover and wheat respectively; while those in sand were 130, 197, 234 mg a.i./kg dw soil. The corresponding NOEC values were 2772.2, 856.2, >4990 mg a.i./kg dw in natural soil and 55.8, 93.4 and 93.4 mg a.i./kg dw in sand. The EC50 values in natural soil, based on the effect on growth were 342, 309, 684 mg a.i./kg dw of soil (based on changes in wet weight) and 537, 634 and 1960 mg a.i./kg dw of soil (based on changes in dry weight) for mustard, red clover and wheat respectively, respectively; while those in sand were 31, 19, 105 mg a.i./kg dw of soil (based on changes in wet weight) and 73, 74 and 141 mg a.i./kg dw soil (based on changes in dry weight) of sand respectively. The difference in toxicity in the two substrates were correlated with the lower bioavailability of test substance in soil due to a stronger adsorption potential. Further, as the toxicity to terrestrial plants in sand is not representative of the natural environment, the EC50 in natural soil was considered as a reasonable worst case for representing toxicity terrestrial plant species. Under the conditions of the study, based on effect on emergence and wet weight changes (growth) red clover was identified to be the most sensitive species with lower NOEC and EC50 value of 856.2 and 309 mg a.i./kg dw soil respectively (Servajean, 2004).
Study 2: A study was conducted to determine the toxicity of the read across substance, C12-16 ADBAC (49.5% active in water) to terrestrial plants, according to OECD Guideline 208, in compliance with GLP. Three plant species:Phaeolus aureus(mung beans)Brassica alba(mustard) andTriticum aestivum(wheat) were used. Each plant species was sown into treated soil and assessed for 14 - 16 days following germination. For each species, groups of 40 seeds (eight replicate pots of five seeds) were sown into a garden loam soil treated with the read across substance. Untreated controls were also included. Treatment levels for the definitive study were based on the results of a preliminary range finding study. The dose levels of the read across substance used were 156, 313, 625, 1250 and 2500 mg a.i./kg dry soil for mung beans and 12, 37, 117, 375 and 1200 mg a.i./kg dry soil for mustard and wheat. After application and sowing, the pots were checked daily and the number of seedlings emerging recorded. Survival and sub-lethal effects were recorded every day following emergence. Plants were harvested 14-16 days after germination and the wet weights were measured. The plants were then dried before being re-weighed to obtain a dry weight measurement. There was no treatment-related effect on the germination and seedling survival of any of the plant species treated with the read across substance up to the highest tested concentrations. The growth inhibition occurred at higher rates of application for all the plant species. For mung bean, there was 25-40 and 50-75% inhibition at 1250 and 2500 mg a.i./kg, respectively. For mustard, there was 75-80 and >80% inhibition at 375 and 1200 mg a.i./kg, respectively and 50-75% for wheat at 1200 mg a.i./kg. Darker pigmentation was observed for all species at the higher rates of application. The 14-16 d EC50 values based on growth inhibition in mung beans, mustard and wheat were determined to be1900, 277 and 670 mg a.i./Kg dry soil respectively. Under the conditions of the study, based on effect on growth, mustard was identified to be the most sensitive species with lower EC50 value of 277 mg a.i./kg dw soil (Gray, 2004).
Based on the above studies, same effect levels and low toxicity potential were concluded in the biocide assessment report on C12-16 ADBAC by RMS Italy. They further stated that:“The great deviation in the effects recorded in sand and natural soil can be attributed to the lower bioavailability of C12-16 ADBAC in natural soil caused by stronger adsorption to the soil particles as consequence of several binding processes. Since the results obtained in the test with silica sand are considered unrealistic worst case, only data from the tests conducted with natural soils are taken into account (this approach was agreed at TMII2013); among these, the most sensitive species was Brassica alba with an EC50 = 277 mg/kg dw soil (US ISC), which is the endpoint to be taken into account at product authorization stage” (ECHA biocides assessment report, 2015). Similar conclusions were drawn in the Coco TMAC biocides assessment report, 2016, where the endpoint was mainly assessed based on read across to DDAC apart from the EQC owned supporting study on C12-16 ADBAC. The lowest EC50 for the most sensitive plant among all the tested species, i.e., EC50 (wet weight growth) = 148 mg/kg dw soil forT. pretenseexposed to DDAC and corrected for MW as EC50 = 111.0 mg a.i./kg dw (98.3 mg a.i./kg ww) was selected for risk assessment (ECHA biocides assessment report, 2016).
In line with the C12-16 ADBAC biocides assessment report and given that the read across to C12-16 ADBAC can be justified for the test substance based on a category approach, the 16-d EC50 value of 277 mg a.i./kg dw of soil obtained forBrassica alba(mustard) due to effects on growth has been considered further for hazard/risk assessment. Additionally, in accordance with the ECHA R.7c guidance (2017), the 16-d NOEC value of 856.2 mg a.i./kg dw of soil obtained forTrifolium pratense(red clover) due to effects on growth can be considered as the long-term equivalent value.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Short-term EC50 or LC50 for soil macroorganisms:
- 7 070 mg/kg soil dw
- Long-term EC10, LC10 or NOEC for soil macroorganisms:
- 125 mg/kg soil dw
Based on the above information and in line with the biocides assessment report on the read across substance C12-16 ADBAC, the 14 d LC50 of 7070 has been selected to express the acute toxicity of the test substance. Further, based on the chronic toxicity study with the read across substance, the 28-d NOEC of 125 mg/kg bw/day has been considered further for hazard/risk assessment.
Short-term toxicity study:
Study 1. A study was conducted to determine the toxicity to soil macroorganisms of the read across substance C12-16 ADBAC (49.5% active) according to OECD Guideline 207, in compliance with GLP. Six groups of forty earthworms (Eisenia foetida) were allocated to an artificial soil containing 0, 953, 1715, 3086, 5556 or 10000 mg a.i./kg soil dw (nominal concentrations). No analytical dose verification was performed. Mortality was recorded on Days 7 and 14. Worms were weighed at the beginning and end of the study. After 7 days, all worms at 10000 and 2 worms at 5556 mg a.i./kg soil dw were dead. By Day 14, one additional worm died at 5556 mg a.i./kg soil dw. A treatment-related reduction in body weight was observed. Group mean body weights were affected by treatment with read across substance at 1715 mg a.i./kg soil dw and above. Under the study conditions, the 7 and 14 d LC50 values were 7160 and 7070 mg a.i./kg soil dw, respectively and the NOEC was 953 mg a.i./kg soil dw (nominal) (Rodgers, 2004).
Study 2. A study was conducted to determine the toxicity to soil macroorganisms of the read across substance, C12 -16 ADBAC (51.7% active) according to OECD Guideline 207, in compliance with GLP. Earthworms (Eisenia foetida) were exposed to a single dose of the read across substance at nominal concentrations of 100, 180, 320, 580 or 1,000 mg/kg dw of artificial soil. No analytical dose verification was performed. The individual live weights of the worms were reported after 14 d of exposure. Other effects (pathological symptoms, behaviour of the worms) were reported after 7 and 14 d of exposure. Results of the reference test with 2 -chloracetamide show that the method was sensitive and valid. The substance did not cause a change in behaviour, weight and mortality of the earthworm at any of the tested concentrations after 14 d of exposure. This was probably due to adsorption onto soil. The highest tested concentration without mortality and any other effects was 1000 mg/kg dw. Under the study conditions, the 14 d NOEC in earthworm was 1000 mg/kg dw (or 517 mg a.i./kg dw) and the 14 d LC0 was > 1000 mg/kg dw (or > 517 mg a.i./kg dw) (Noack, 1999).
Based on the above two studies, the same effect levels were concluded in the biocide assessment report on C12-16 ADBAC by RMS Italy. They further stated that:“The findings of the two tests, although different in absolute values, are not in contrast. Since the second test provides a “higher than” value corresponding to a complete lack of lethal or sublethal effects, the 14d LC50 = 7070 mg/kg dry soil (US ISC) is selected to express the acute toxicity of Alkyl (C12-16) dimethylbenzyl ammonium chloride to soil dwelling invertebrates.”
Long-term toxicity study:
A study was conducted to determine the effects of read across substance (50% active in water) on mortality, biomass and the reproductive potential of the earthworm speciesEisenia fetida(Annelida, Lumbricidae), according to the OECD TG 222, in compliance with GLP. The study was conducted under static conditions over 8 weeks with the read across substance concentrations 125, 250, 500, 1000, 2000 mg//kg solid dry weight (SDW) corresponding to 62.5, 125, 250, 500, 1000 mg a.i./kg SDW. Each application rate was mixed into artificial soil containing 5% peat. A control including untreated artificial soil was tested under the same conditions as the read across substance treatments. A total of 80 test organisms were divided equally into 8 control replicates adnd another total of 40 test organisms were divided equally into 4 replicates for each read across substance treatment (i.e., 10 earthworms per replicate). They had an individual body weight between 0.36 and 0.55 g at the experimental starting. Each concentration level and control were analysed via LC-MS/MS analysis on Day 0, Day 28 and Day 55 using pooled samples of all replicates. The measured concentrations of the pooled samples of replicates were within the range of 83 to 101 % of the nominal values on Day 0, demonstrating the right preparation of the tested concentrations. After 28 days of exposure in soil, no read across substance-related earthworm mortalities (<10%), pathological symptoms or changes in the behaviour of adult earthworms were observed in the control or all read across substance concentrations. There were no statistically significant differences in earthworm body weights in all read across substance concentrations compared to the control. After an additional 4 weeks, the reproduction rate (average number of juveniles produced) was 83 juveniles in the control and ranged from 18 to 74 juveniles in the read across substance treatment rates. There were no statistically significant differences in earthworm reproduction in the treatment rates 125 and 250 mg read across substance/kg SDW compared to the control. However, at the read across substance concentrations, 500 to 2000 mg read across substance/kg SDW the earthworm reproduction was statistically significantly reduced. All validity criteria recommended by the test guidelines were fulfilled. Under the study conditions, the LOEC (mortality, biomass), NOEC (mortality, biomass), LOEC (reproduction), NOEC (reproduction) and EC50 (reproduction) values for read across substance were reported to be >2000, ≥2000, 500, 250 and 589 mg read across substance/kg SDW, respectively (equivalent to >1000, ≥1000, 250, 125 and 295 mg a.i./kg SDW, respectively). Based on the results of the read across study, similar effect levels can be considered for the test substance.
Therefore, based on the above information and in line with the biocides assessment report on the read across substance C12 -16 ADBAC, the 14 d LC50 of 7070 has been selected to express the acute toxicity of the test substance. Further, based on the chronic toxicity study with the read across substance, the 28-d NOEC of 125 mg/kg bw/day has been considered further for hazard/risk assessment.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Short-term EC50 for soil microorganisms:
- 153 mg/kg soil dw
- Long-term EC10 or NOEC for soil microorganisms:
- 83 mg/kg soil dw
In line with the C12 -16 biocides assessment report and based on the results of the read across study, the lower 28d EC50 = 153 mg a.i./kg dw and a 28d EC10 = 83 mg a.i./kg dw soildue to inhibition of microorganisms has been considered further for hazard/risk assessment.
Study 1. A study was conducted to determine the toxicity of the read across substance, C12-16 ADBAC (49.9% active in water) to soil microorganisms, according to OECD Guideline 216, in compliance with GLP. In this study, the inhibition of microbial nitrogen transformation was investigated in sandy loam soil by evaluating the nitrite, nitrate and ammonium formation following 28 d exposure to the read across substance. A volume of 6.04 mL of deionized water containing the read across substance was added to 50-g of soil. The samples were incubated for 7 d at 20°C and at 10% of its water holding capacity. The samples were dosed with read across substance at nominal concentrations 0, 50, 100, 200, 400, 800, 1600, 3200 and 6400 mg a.i./kg soil ww. Analytical dose verification of the stock solutions indicated good correlation with the nominal concentrations. Therefore, doses were presented as nominal concentrations. The nitrogen transformation measurements were carried out at the beginning of the test and at the end at Day 28. The activity of the microorganisms transforming nitrogen in soil was slightly inhibited at 50 mg a.i./kg soil ww. The EC50 calculated was 130 mg a.i./kg soil ww with 95% confidence limits of 80 and 190 mg a.i./kg soil ww. The EC10, EC20 and EC80 of the read across substance were determined at 70, 90 and 200 mg a.i./kg soil ww respectively. In soil not only formation of nitrate occurs but also reduction of nitrate to nitrogen gas by denitrifying microorganisms. Decrease of the nitrate concentrations in the soil was observed at 400 mg a.s./kg soil ww and higher after 28 d. This was probably the result of the activity of these denitrifying microorganisms. The denitrifying microorganisms were inhibited at 6400 mg a.i./kg soil ww, as only a limited amount of the nitrate was removed after 28 d at this concentration. Under the study conditions, the 28 d EC50 and EC10 values were determined to be at 130 and 70 mg a.i./kg soil ww (i.e., equivalent to 153 and 83 mg a.i./kg soil dw) respectively (van Ginkel, 2004).
Study 2. A study was conducted to determine the toxicity of the read across substance, C12-16 ADBAC (49-51% active in water) to soil microorganisms, according to OECD Guideline 216 and 217, and US EPA OPPTS 850.5100, in compliance with GLP. In this study, the effects of the read across substance on carbon mineralization and nitrogen transformation activity of soil micro-organisms were investigated in two soil types (sandy loam soil and a low humic content sand) by evaluating nitrite, nitrate, ammonium and carbon dioxide formation following 28 d exposure. Fifty grams dry weight of soil samples were mixed with lucerne meal (13:1 carbon:nitrogen) and placed in 100 mL bottles. The samples were incubated in the dark at 20±2°C for 28 d. The moisture content of the samples was checked weekly. The samples were dosed with read across substance at nominal concentrations 0, 10, 100 and 1000 µg a.i./g soil dw. No analytical dose verification was performed for the read across substance. Samples were taken to determine nitrogen metabolite content on days 5 and 28 and the CO2 evolution was determined on Days 5 – 8 and 25 – 28. No significant reduction in ammonium formation was observed. The difference in the CO2 production and nitrogen transformation between the treated and untreated soil samples did not exceed 25% after 28 d of incubation. The highest inhibition recorded was 82.5% in the nitrite formation rate after 5 d at 10 mg a.i./kg soil dw in the sandy loam soil. After 28 d of incubation, however, no relevant effect was observed (<25% reduction). Therefore, it was not necessary to extend the test beyond 28 d. Under the conditions of the study, the read across substance was therefore considered to have a low potential for adversely affecting the microbial functions of sandy loam and low humic content sand soils and the 28 d EC50 and NOEC were considered to be at >1000 and ≥1000 µg a.i./g soil dw respectively (de Vette, 2001).
Based on the above studies, same effect levels and low toxicity potential were concluded in the biocide assessment report on C12-16 ADBAC by RMS Italy. They further stated that: “The studies from the two dossiers, although all rated 1, show marked difference in the results, even when the soil characteristics were similar like in the case of tests conducted with sandy loam soils. The endpoint with the lowest values is therefore selected to be taken into account, i.e., 28d EC50 = 153 mg a.i./kg dw (130 mg/kg wwt soil) and a 28d EC10 = 83 mg a.i./kg dw soil (70 mg a.i./kg ww soil), retrieved from the EQC dossier.”(ECHA biocides assessment report, 2015). Similar conclusions were drawn in the Coco TMAC biocides assessment report, 2016, where the endpoint was mainly assessed based on read across to DDAC along with the EQC owned supporting study on C12-16 ADBAC. The lowest 28d EC50 = 101.3 mg a.s. /kg dw (corrected for MW) and 28d EC10 = 59.3 mg a.s. /kg dw (corrected for MW) from the study on DDAC was selected for risk assessment.
In line with the C12 -16 biocides assessment report and gven that the read across to C12-16 ADBAC can be justified for the test substance based on a category approach, the lower 28d EC50 = 153 mg a.i./kg dw and a 28d EC10 = 83 mg a.i./kg dw soil due to inhibition of microorganisms has been considered further for hazard/risk assessment.
- Reason / purpose for cross-reference:
- data waiving: supporting information
Reference
- Hazard assessment conclusion:
- PNEC aqua (freshwater)
- PNEC value:
- 0.415 µg/L
- Assessment factor:
- 10
- Extrapolation method:
- assessment factor
- PNEC freshwater (intermittent releases):
- 0.37 µg/L
- Hazard assessment conclusion:
- PNEC aqua (marine water)
- PNEC value:
- 0.042 µg/L
- Assessment factor:
- 100
- Extrapolation method:
- assessment factor
- PNEC marine water (intermittent releases):
- 0.037 µg/L
- Hazard assessment conclusion:
- PNEC STP
- PNEC value:
- 0.48 mg/L
- Assessment factor:
- 1
- Extrapolation method:
- assessment factor
- Hazard assessment conclusion:
- PNEC sediment (freshwater)
- PNEC value:
- 68 mg/kg sediment dw
- Extrapolation method:
- equilibrium partitioning method
- Hazard assessment conclusion:
- PNEC sediment (marine water)
- PNEC value:
- 6.8 mg/kg sediment dw
- Extrapolation method:
- equilibrium partitioning method
- Hazard assessment conclusion:
- no hazard identified
- Hazard assessment conclusion:
- PNEC soil
- PNEC value:
- 1.66 mg/kg soil dw
- Assessment factor:
- 50
- Extrapolation method:
- assessment factor
- Hazard assessment conclusion:
- no potential for bioaccumulation
Based on the results from the available studies with the test or read across substances, daphnia has been identified to be the most sensitive species. The short-term 48 h EC50 value based on a study with the test substance in Daphnia was determined to be 0.037 mg a.i./L (nominal) and the lowest long-term 21-day NOEC value based on a read across study with C12-16 ADBAC in daphnia was determined at 0.00415 mg/L (measured). Therefore, based on the available results, the test substance C18 TMAC warrants a classification as ‘Aquatic Acute 1’ and ‘Aquatic Chronic 1; H410: Very toxic to aquatic life with long lasting effects’ according to EU CLP criteria (Regulation 1272/2008/EC). M factors to be applied are 10 for acute and 1 for chronic toxicity.
Data source
Materials and methods
Results and discussion
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.