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EC number: 203-327-9 | CAS number: 105-75-9
- 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

Long-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- fish early-life stage toxicity
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2013-2014
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- According to OECD 210, : “Fish, Early-life Stage Toxicity Test”, Adopted July 17, 1992. In addition, the procedures were designed to meet the test methods of the following guideline and guidance document:• EPA Ecological Effects Test Guidelines, OPPTS 850.1400, Fish Early-Life Stage Test 'Public Draft', EPA 712-C-96-121, April 1996.• Guidance document on aquatic toxicity testing of difficult substances and mixtures, OECD series on testing and assessment number 23, December 14, 2000.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 210 (Fish, Early-Life Stage Toxicity Test)
- Deviations:
- yes
- Remarks:
- 1. Semi-static range-finding test: The temperature of the old medium at day 1 was 28°C. Evaluation: This did not affect the embryos. 2. Final test: Illumination has been continuous. Evaluation: Embryos and larvae were not affected.
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- Samples were taken on day 0, day 1, day 7, day 14, day 21, day 28 and day 35. Measured concentrations were almost always lower than target and not stable. It was therefore considered appropriate to calculate the mean measured concentrations in order to determine the effect parameters. The mean measured concentrations were calculated to be: 0.0074, 0.062, 0.23, 1.2 and 5.7 mg/l.
- Vehicle:
- no
- Details on test solutions:
- 0.050, 0.16, 0.50, 1.6 and 5.0 mg/l Test medium without test substance or other additives (blank-control) and one control containing test medium with the additives used in the treatment of the stock solutions (DMF-control).
- Test organisms (species):
- Pimephales promelas
- Details on test organisms:
- Fathead minnow (Pimephales promelas, Teleostei Cyprinidae) Rafinesque, In house culture.
- Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 35 d
- Hardness:
- Total hardness ranged between 196 and 250 mg calcium carbonate per litre. This was according to the value described in the protocol, i.e. >140 mg/l as CaCO3.
- Test temperature:
- The average temperature in the control and the treatment groups varied between 23.1 and 25.4°C. The temperature continuously measured in the control vessels ranged between 23.3 and 25.7°C. This was within the range described in the Protocol: 25 ± 2°C.
- pH:
- Oxygen concentrations varied between 6.8 and 8.6 mg/l during the test period, which is >60% of oxygen saturation at 25°C as prescribed by the Protocol. .
- Dissolved oxygen:
- Oxygen concentrations varied between 6.8 and 8.6 mg/l during the test period, which is >60% of oxygen saturation at 25°C as prescribed by the Protocol.
- Salinity:
- Adjusted ISO medium, formulated using RO-water (tap-water purified by reverse osmosis; GEON Waterbehandeling, Berkel-Enschot, The Netherlands) with the following composition:CaCl2.2H2O211.5 mg/lMgSO4.7H2O 88.8 mg/lNaHCO3 46.7 mg/lKCl 4.2 mg/l
- Nominal and measured concentrations:
- Nominal: 0.050, 0.16, 0.50, 1.6 and 5.0 mg/l Measured: 0.0074, 0.062, 0.23, 1.2, 5.7 mg/l
- Details on test conditions:
- The spawning tank is equipped with a substrate (pvc-tube), which enables collection of the fertilised eggs.Feeding brood stock: Frozen brine shrimp Nauplii and pelleted fish food (Cyprico Crumble Excellent (300-500 um), Coppens International bv, Helmond, The Netherlands).Time of fertilisation: Males and females were put together in spawning tanks and spawning started the following day approximately 1 to 2 hours after lights were switched on.
- Reference substance (positive control):
- yes
- Remarks:
- DMF
- Duration:
- 35 d
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 0.23 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: embryonic survival
- Duration:
- 35 d
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 0.062 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: larval survival
- Duration:
- 35 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.007 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: larval growth
- Details on results:
- Overall survival of fertilised eggs in the DMF-control was ≥66% until hatching was complete (i.e. 100% after 6 days of exposure). No significant effects on mortality of fish embryo’s and juvenile fish were observed at test concentrations up to and including 0.50 mg/l during the 7-day range-finding test. At the highest target concentration of 5.0 mg/l all embryos died within the first two days of exposure.Samples taken from all test concentrations before the start of the test showed that the analytical results were variable and could not be improved before the start of the test. Samples taken from the stock solutions at day 1 (fresh) and at days 2 and 4 (old) showed that the concentrations in the four highest stocks were in agreement with target (90-116%), while the concentration in the lowest stock was slightly to high at the start (123% of target) and decreased to 80% of target after 72 hours.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The results of the ELS test led to the following conclusions:1. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on embryonic survival at concentrations up to and including 0.23 mg/l. Hence, the NOEC and LOEC for embryonic survival were 0.23 and 1.2 mg/l, respectively;2. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval survival at concentrations up to and including 0.062 mg/l. Hence, the NOEC and LOEC for larval survival were 0.062 and 0.23 mg/l, respectively;3. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval growth at concentrations up to and including 0.0074 mg/l. Hence, the NOEC and LOEC for larval growth were 0.0074 and 0.062 mg/l, respectively
- Executive summary:
Fish early-life stage toxicity test with Fumaric acid di-n-butyl ester.
The study procedures described in this report were based on theOECD guidelines for Testing of Chemicals: Guideline No. 210, 1992. In addition,the procedures were designed to meet the test methods and validity criteria of theEPA Ecological Effects Test Guidelines, 'Public Draft', EPA 712-C-96-121, 1996 andthe OECD series on testing and assessment number 23, 2000.
The reproduction test was performed using a flow-through system with target concentrations of 0.050, 0.16, 0.50, 1.6 and 5.0 mg/l, which were based on the results of two preceding range-finding tests. A blank- and solvent-control (DMF) were also included.
In the flow-through system the dilution water was dosed separately from the test substance stock solutions into mixing vessels. Stock solutions in DMF were a factor of 10,000 higher than in the target concentrations. The dosed volumes and the dilution water were mixed under continuous stirring in the mixing vessels before entering the test vessels. The dosing was computer controlled, and the system was checked daily. The ELS testwas performed with three replicates containing 20 eggs per replicate for each concentration and controls.The test started by placing fertilised eggs in stainless steel test vessels. During the embryonic and larval phases, the fish were observed for effects on development, appearance and swimming behaviour. At the end of the test (day 35), the surviving fish were measured and weighed.
During the study, samples for analyses were taken at the start of exposure and on days 7, 14, 21, 28 and 35. Measured concentrations were almost always lower than target and not stable. It was therefore considered appropriate to calculate the mean measured concentrations in order to determine the effect parameters. The mean measured concentrations were calculated to be: 0.0074, 0.062, 0.23, 1.2 and 5.7 mg/l.
The study met the acceptability criteria prescribed by the protocol and was considered valid.
The results of the ELS test led to the following conclusions:
1. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on embryonic survival at concentrations up to and including 0.23 mg/l. Hence, the NOEC and LOEC for embryonic survival were 0.23 and 1.2 mg/l, respectively;
2. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval survival at concentrations up to and including 0.062 mg/l. Hence, the NOEC and LOEC for larval survival were 0.062 and 0.23 mg/l, respectively;
3. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval growth at concentrations up to and including 0.0074 mg/l. Hence, the NOEC and LOEC for larval growth were 0.0074 and 0.062 mg/l, respectively.
Reference
The pH varied between 7.4 and 7.8 during the test period, which was within the range described in the Protocol
Description of key information
The results of the ELS test led to the following conclusions:
1. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on embryonic survival at concentrations up to and including 0.23 mg/l. Hence, the NOEC and LOEC for embryonic survival were 0.23 and 1.2 mg/l, respectively; 2. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval survival at concentrations up to and including 0.062 mg/l. Hence, the NOEC and LOEC for larval survival were 0.062 and 0.23 mg/l, respectively;
3. Fumaric acid di-n-butyl ester did not induce any statistically significant effects on larval growth at concentrations up to and including 0.0074 mg/l. Hence, the NOEC and LOEC for larval growth were 0.0074 and 0.062 mg/l, respectively
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 7.4 µg/L
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