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EC number: 907-131-0 | CAS number: -
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods with acceptable restrictions
- Remarks:
- Study conducted according to Environment Canada test method.
- Qualifier:
- according to guideline
- Guideline:
- other: Test for Survival and Growth in Sediment Using the Freshwater Amphipod Hyalella azteca, EPS 1/RM/33 (EC 1997)
- Principles of method if other than guideline:
- Environment Canada test method
- GLP compliance:
- not specified
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Samples from the control, low, medium and high treatments were collected at the start and end of each test, and analysed
- Vehicle:
- no
- Details on test solutions:
- - The stock and test solutions were prepared in SAM-5S reconstituted water as per Borgmann, 1996.
- The water was aerated at test temperature at least overnight prior to use in the test. - Test organisms (species):
- other aquatic crustacea: Hyalella azteca
- Details on test organisms:
- TEST ORGANISM
- Feeding during test
- Food type: YCT
- Amount: 1.3 mL
- Frequency: on Day 0 and 0.5 mL on Day 2 of the test.
ACCLIMATION
- Acclimation period: for 5 days prior to use in the tests
- Acclimation conditions (same as test or not): same
- Type and amount of food: 10 mL each of YCT and Tetrafin
- Feeding frequency: twice daily
- Health during acclimation (any mortality observed): Total mortality during this period was 1.25%. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- 124 mg/L as CaCO3 (measured by EDTA titration)
- Test temperature:
- 21 - 25 °C
- Nominal and measured concentrations:
- Five nominal test concentrations and a control were tested. Analytical recovery of the test concentrations at test start and end were generally within 20% of nominal concentrations: 83-90%
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 250 mL glass beaker
- Type: The test chambers were covered with a plexiglass sheet
- Fill volume: 200 mL
- Aeration: The water was aerated at test temperature at least overnight prior to use in the test.
- Renewal rate of test solution: Test solutions were not renewed during the tests.
- No. of organisms per vessel: 10
- No. of vessels per concentration: 4
- No. of vessels per control: 4
TEST MEDIUM / WATER PARAMETERS
- Source/ preparation of dilution water: The stock and test solutions were prepared in SAM-5S reconstituted water as per Borgmann, 1996. This water was prepared by adding 8.82 g CaCl2•2H2O, 1.81 g MgSO4, 0.06 g NaBr, 5.04 g NaHCO3, 0.22 g KCl to 60 L of deionised water.
- Alkalinity: 53 mg/L as CaCO3
OTHER TEST CONDITIONS
- Photoperiod: 16 h light / 8 hours dark
EFFECT PARAMETERS MEASURED:
The test chambers were monitored on Days 2 and 4 for number of dead neonates. Measurements of dissolved oxygen concentrations, temperature, and pH, were taken at the start and end of the test. Conductivity was measured at test initiation. - Reference substance (positive control):
- yes
- Remarks:
- copper sulphate
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 43 500 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- analytically verified
- Basis for effect:
- mortality
- Remarks on result:
- other: CI95%:39400 - 48100
- Results with reference substance (positive control):
- The resulting LC50 (203 μg Cu/L with 95% confidence limits of 177 and 233 μg/L) were within two standard deviations of previous tests (35 and 389 μg/L).
- Reported statistics and error estimates:
- The 96-hr LC50 with 95% confidence limits were calculated using the trimmed Spearman-Karber (0-10% trim) method or maximum likelihood probit method in the statistical program, ToxCalc™ (Version 5.0.23j), a Microsoft Excel-based software application (Tidepool Scientific Software 1994-2006).
- Validity criteria fulfilled:
- yes
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- (Q)SAR
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Justification for type of information:
- 1. SOFTWARE
Estimation Programs Interface (EPI) Suite for Microsoft Windows, v4.11 (US EPA, 2012)
2. MODEL (incl. version number)
ECOSAR v2.00
3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
See section 'Test Material'.
4. SCIENTIFIC VALIDITY OF THE (Q)SAR MODEL
See attached QMRF.
5. APPLICABILITY DOMAIN
See attached QPRF.
6. ADEQUACY OF THE RESULT
- The model is scientifically valid (see attached QMRF).
- The model estimates the toxicity to aquatic organisms: Daphnids: 48-h EC50; this data can be used to support the assessment regarding the toxicity of a substance to
aquatic organisms (see also attached QPRF). - Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- ECOSAR v2.00: Estimation of acute toxicity to Dpahnid for chemical class "Neutral Organic SAR (Baseline Toxicity)"
- GLP compliance:
- no
- Test organisms (species):
- other: Daphnid
- Water media type:
- freshwater
- Total exposure duration:
- 48 h
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 115 220 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Remarks on result:
- other: ECOSAR chemical class: "Neutral Organic SAR (Baseline Toxicity)"; The substance is in the applicability domain of the model.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- (Q)SAR
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Justification for type of information:
- 1. SOFTWARE
Estimation Programs Interface (EPI) Suite for Microsoft Windows, v4.11 (US EPA, 2012)
2. MODEL (incl. version number)
ECOSAR v2.00
3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
See section 'Test Material'.
4. SCIENTIFIC VALIDITY OF THE (Q)SAR MODEL
See attached QMRF.
5. APPLICABILITY DOMAIN
See attached QPRF.
6. ADEQUACY OF THE RESULT
- The model is scientifically valid (see attached QMRF).
- The model estimates the toxicity to aquatic organisms: Daphnids: 48-h EC50; this data can be used to support the assessment regarding the toxicity of a substance to
aquatic organisms (see also attached QPRF). - Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- ECOSAR v2.00: Estimation of acute toxicity to Dpahnid for chemical class "Neutral Organic SAR (Baseline Toxicity)"
- GLP compliance:
- no
- Test organisms (species):
- other: Daphnid
- Water media type:
- freshwater
- Total exposure duration:
- 48 h
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 256 258 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- act. ingr.
- Basis for effect:
- mortality
- Remarks on result:
- other: ECOSAR chemical class: "Neutral Organic SAR (Baseline Toxicity)"; The substance is in the applicability domain of the model.
Referenceopen allclose all
The tests were considered valid as none of control amphipods died or displayed atypical or stressed behaviour during the test. A reference toxicant (positive control) test was conducted with copper sulphate. The resulting LC50 (203 µg Cu/L with 95% confidence limits of 177 and 233 µg/L) were within two standard deviations of previous tests (35 and 389 µg/L).
Description of key information
Overall, it can be concluded that with high probability the test substance is acutely not harmful to aquatic invertebrates.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- LC50
- Effect concentration:
- 43 500 mg/L
Additional information
QSAR-disclaimer
In Article 13 of Regulation (EC) No 1907/2006, it is laid down that information on intrinsic properties of substances may be generated by means other than tests, provided that the conditions set out in Annex XI (of the same Regulation) are met.
According to Annex XI of Regulation (EC) No 1907/2006 (Q)SAR results can be used if (1) the scientific validity of the (Q)SAR model has been established, (2) the substance falls within the applicability domain of the (Q)SAR model, (3) the results are adequate for the purpose of classification and labelling and/or risk assessment and (4) adequate and reliable documentation of the applied method is provided.
For the assessment of the substance (Q)SAR results were used for the estimation of the acute toxicity to aquatic invertebrates. The criteria listed in Annex XI of Regulation (EC) No 1907/2006 are considered to be adequately fulfilled and therefore the endpoint(s) sufficiently covered and suitable for risk assessment.
Assessment
2,2'-(ethylenedioxy)diethanol 3,6,9-trioxaundecane-1,11-diol (EC 907-131-0) is a multi-constituent substance. The main constituents of EC 907-131-0 are triethylene glycol (TGE, CAS 112-27-6, 10-80% w/w) and tetraethylene glycol (Tetra-EG, CAS 112-60-7, 10-80% w/w). Since no data on the long-term toxicity to fish of the reaction mass of 2,2'-(ethylenedioxy)diethanol 3,6,9-trioxaundecane-1,11-diol are available, the assessment is based on the available data for the main components triethylene glycol (CAS 112-27-6) and tetraethylene glycol (112-60-7).
For CAS 112-27-6 a kes study is available. This test investigated the short-term toxicity to aquatic crustacea (Hyalella azteca) (PTAC, 2006). Test organisms were exposed to five test concentrations of the test substance and a control for 96 hours under freshwater static conditions. Analytical recovery of the test concentrations at test start and end were generally within 20% of nominal concentrations: 83-90%. Therefore, effect levels are reported as nominal. The 96-h LC50 for the test substance was determined to be 43500 mg/L.
These results are supported with the estimated value for CAS 112 -27 -6, which was derived from a valid QSAR model (ECOSAR v2.0; BASF SE, 2022). The 48 -h LC50 for the substance was predicted to be 115220 mg/L. The substance was within the applicability domain of the model.
Overall, it can be concluded that with high probability the test substance is acutely not harmful to aquatic invertebrates.
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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