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EC number: 222-720-6 | CAS number: 3586-55-8
- 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

Short-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- Adopted July 17th, 1992
- Deviations:
- yes
- Remarks:
- After 24 h of incubation, the temperature of the medium was lower than the range (21-25°C) proposed by the Guideline. This deviation is considered by the authors as having no influence on the integrity and validity of the study.
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: TS in samples with nominal concentrations of 25, 50 and 100 mg/L; concentration were determined daily
- Vehicle:
- no
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Source: Tagis-Aquarium and Aquafarm Ryba (both Germany)
- Length at study initiation: approx. 3 cm - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Test temperature:
- 20.0 – 22.6°C
- pH:
- 7.52 – 8.42
- Dissolved oxygen:
- 7.6 – 8.2 mg/L
- Nominal and measured concentrations:
- Nominal concentrations:
Screening test: 1, 10, 100 mg/L + control
Main test: 6.25, 12.5, 25, 50, 100 mg/L + control - Details on test conditions:
- TEST SYSTEM
- Type: open. However, the test was run semistatically due to probable volatility of the test substance.
- Renewal rate of test solution: Daily renewal
- No. of organisms per vessel: Screening test: 3 fish / 3 L solution; Main test: 7 fish / 3 L solution
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Tap water from municipal drinking water supply
- Intervals of water quality measurement: pH, oxygen content and temperature checked at the beginning and daily after 24 h.
OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: light/dark cycle : 16 h / 8 h
EFFECT PARAMETERS MEASURED:
Daily examination for dead animals - Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 71 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other:
- Remarks:
- LC0 and LC100 were directly taken from the concentrations being tested. LC50 was calculated as the geometric mean between LC0 and LC100.
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- 50 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC100
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- Effects other than mortality were not recorded.
No dead fish in the control vessels. - Sublethal observations / clinical signs:
Results of determination ofthe test substance in the test medium:
Sampling time [h]
Nominal Conc. [mg/L]
Measured Conc. [mg/L]
to
100
121.05
to
50
63.46
to
25
30.91
to
control
<2
t24h
50
60.74
t24h
25
20.65
to’(24h)
100
88.60
to’(24h)
50
47.92
to’(24h)
25
23.86
t48h
100
84.99
t48h
50
62.33
t48h
25
19.58
t72h
100
119.15
t72h
50
40.02
t72h
25
31.30
to’’’(72h)
50
37.05
to’’’(72h)
25
31.26
t96h
50
58.09
t96h
25
18.10
The results in the table were not corrected for the recoveries obtained by the analytical methodhe mean recovery rate was 100%.
The authors stated that the test solutions showed no significant loss of the test substance. Therefore, nominal concentrations can be considered as the effective concentrations.
Applicant note: Some individually-measured concentrations deviate by more than 20% from the nominal. However, the mean values were within 20% of the nominal concentrations. A general trend towards loss of formaldehyde in 24 h old solutions, compared to freshly prepared media, cannot be observed. Therefore, the demands of the Guideline (stability ≥ 80% of nominal) can be regarded as fulfilled.
Results of main test:
Test substance
Concentration
(nominal)[mg/L]
Mortality
Number
Percentage
24 h
48 h
72 h
96 h
24 h
48 h
72 h
96 h
Control
Not reported
0
0
0
0
100
14
86
100
100
50
0
0
0
0
25
0
0
0
0
12.5
0
0
0
0
6.25
0
0
0
0
Temp.[°C]1)
20.0-20.2
21.1
22.4-22.6
22.6
pH freshly prepared
7.61-7.86
7.52-7.86
7.76-7.91
-
pH after 24 h
8.23-8.40
8.28-8.42
8.27-8.40
8.12-8.38
Oxygen [mg/L]
7.6-8.1
7.7-8.1
7.7-8.2
7.6-8.1
1) After 24 h test temperature was lower than the range proposed by the Guideline (21-25°C). This deviation is not considered by the authors to have an influence on the integrity of the study.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The LC50 was calculated as the geometric mean between LC0 and LC100 representing 71 mg/L of the test substance.
- Executive summary:
The reaction products of ethylene glycol with paraformaldehyde were tested for acute toxicity towards Danio rerio according to OECD-Test Guideline 203. 7 fish were exposed in a semistatic system to 5 concentrations of the test substance between 6.25 and 100 mg/L and a control group. The test solutions were prepared in drinking water and renewed daily. Test duration was 96 hours and the test solutions were examined daily for dead fish. Oxygen concentrations, temperature and pH of the medium were measured in the same intervals. Analysis of the formaldehyde concentrations was performed daily by HPLC.
The test substance was found to be acutely harmful towards Danio rerio. All results refer to the nominal concentrations due to formaldehyde concentration being shown stable within the incubation period.
A clear concentration-response relationship can be established from the study results. Lethal effects were observed only at a concentration of 100 mg/L. The next concentration of the geometric series exhibited no toxicity (manifest as mortality). Therefore, the LC50 was calculated as the geometric mean between LC0 and LC100 representing 71 mg/L of the test substance.
The test substance EGForm hydrolyses rapidly and completely in the test medium, forming ethylene glycol and formaldehyde. Formaldehyde is expected to dominate the toxicity of EGForm in aqueous solutions. Dissolved formaldehyde is not expected to be volatile, and no losses due to adsorption are to be expected.
Analysis of the formaldehyde concentrations during the test proved that no significant losses occurred with respect to the mean measured values. Individual results, however, are deviating by more than 20% of the nominal concentration. A general trend towards loss of formaldehyde in 24 h old solutions, compared to freshly prepared media, cannot be observed. Therefore, the effective concentrations can be considered to be equal to the nominal concentrations.
Reference
Description of key information
In a study on the acute toxicity of the test substance towards fish the LC50 was determined to be 71 mg/L employing the zebrafish (Danio rerio) as the test organism.
The acute 96 h LC50 value of ethylene glycol to P. promelas was determined to 72860 mg/L.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 71 mg/L
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