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EC number: 204-800-2 | CAS number: 126-73-8
- 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 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:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Proprietary guideline study, cited in OECD SIDS. Officially accepted and peer-reviewed by the OECD SIDS evaluation programme.
- Qualifier:
- according to guideline
- Guideline:
- EPA OTS 795.1200 (Gammarid Acute Toxicity Test)
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- not specified
- Details on sampling:
- No information available
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- other aquatic crustacea: Hyalella azteca
- Details on test organisms:
- The Gammarid Hyalella azteca, length 1-2mm
- Test type:
- flow-through
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- Nominal
- Details on test conditions:
- No information available
- Reference substance (positive control):
- not specified
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- < 1.9 mg/L
- Nominal / measured:
- nominal
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 2.4 mg/L
- Nominal / measured:
- nominal
- Details on results:
- No further information available
- Results with reference substance (positive control):
- No information available
- Reported statistics and error estimates:
- No information available
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 96 hour NOEC of tributyl phosphate to the Gammarid Hyalella azteca was < 1.9 mg/L, and the 96 hour LC50 was 2.4mg/L.
- Executive summary:
The 96-hour NOEC of tributyl phosphate to theGammarid Hyalella aztecawas < 1.9 mg/L, and the 96 hour LC50was 2.4 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Proprietary GLP study, summarised in OECD SIDS (secondary source). Officially accepted and peer-reviewed by the OECD SIDS evaluation programme.
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Daphnia acute toxicity test
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- yes
- Details on sampling:
- No information available
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna
- Test type:
- flow-through
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- No information available
- Details on test conditions:
- No information available
- Reference substance (positive control):
- not specified
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.75 mg/L
- Nominal / measured:
- not specified
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 2.6 mg/L
- Nominal / measured:
- not specified
- Details on results:
- No further information
- Results with reference substance (positive control):
- No information available
- Reported statistics and error estimates:
- No information available
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 48 hour EC50 of tributyl phosphate in Daphnia was 2.6 mg/l.
- Executive summary:
The 48 -hour EC50of tributyl phosphate inDaphniawas 2.6 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Proprietary GLP study similar to guidelines, summarised in OECD SIDS (secondary source). Officially accepted and peer-reviewed by the OECD SIDS evaluation programme.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- no
- Details on sampling:
- No details provided
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna
- Test type:
- not specified
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- Nominal
- Details on test conditions:
- No information available
- Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.8 mg/L
- Nominal / measured:
- nominal
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 9 mg/L
- Nominal / measured:
- nominal
- Details on results:
- No further information
- Results with reference substance (positive control):
- Not relevant
- Reported statistics and error estimates:
- No information available
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 48h NOEC of tributyl phosphate in Daphnia magna was 1.8mg/L.
- Executive summary:
The 48 -hour NOEC of tributyl phosphate in Daphnia magna was 1.8 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published peer reviewed study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Daphnia magna acute immobilisation
- GLP compliance:
- no
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant. - Analytical monitoring:
- not specified
- Details on sampling:
- No information available.
- Vehicle:
- not specified
- Details on test solutions:
- No information available.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna Straus; standardised test strain IRCHA
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 24 h
- Post exposure observation period:
- No information available.
- Hardness:
- No information available.
- Test temperature:
- No information available.
- pH:
- No information available.
- Dissolved oxygen:
- No information available.
- Salinity:
- No information available.
- Nominal and measured concentrations:
- Not relevant
- Details on test conditions:
- No information available.
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EC0
- Effect conc.:
- 5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 30 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 25-36
- Duration:
- 24 h
- Dose descriptor:
- EC100
- Effect conc.:
- 41 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- The 24 hour EC50 value for tributyl phosphate in Daphnia is 30 mg/L.
- Results with reference substance (positive control):
- Not relevant.
- Reported statistics and error estimates:
- No information available.
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 24 hour EC50 value for tributyl phosphate in Daphnia is 30 mg/L.
- Executive summary:
The acute toxicity of tributyl phosphate was investigated in a 96-hour study in Daphnia magna. The 24 hour EC50 value for tributyl phosphate in Daphnia was found to be 30 mg/L under the conditions of this study.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 22 August 1985 to 23 August 1885
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Laboratory data
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- not specified
- Details on sampling:
- No information provided
- Vehicle:
- no
- Details on test solutions:
- No information provided
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organsims were 6 - 24 hours old. They were from Laborzucht der Bayer AG Leverkusen.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 24 h
- Post exposure observation period:
- No information provided
- Hardness:
- No information provided
- Test temperature:
- 20 - 22 °C
- pH:
- after 24 hours, the pH ranged from 7.8 to 8.4
- Dissolved oxygen:
- after 24 hours, O2 ranged from 8.5 - 9.0 mg/L
- Salinity:
- No information provided
- Nominal and measured concentrations:
- Main study 1: nominal concentrations used were 2.5, 5.0, 7.5, 10.0, 20.0, 30.0, 40.0, 50.0, 75 and 100
Main study 2: nominal concentrations used were 5, 7.5, 10, 20, 30, 40, 50, 75 and 1000 mg/L. - Details on test conditions:
- The test was carried out in cylindrical test vessels that contained 10 mL of the test solution. No aeration was used in the test. It was a static system. No solubiliser was used. There were 5 daphnia per test vessel.
- Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: Pre-test
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 5.8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: Main study 1
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 28.75 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: Main study 2
- Details on results:
- No further information
- Results with reference substance (positive control):
- The EC50 was 2.38 mg/L.
- Reported statistics and error estimates:
- No information provided
- Validity criteria fulfilled:
- yes
- Conclusions:
- EC50 values of between 5 -28.75 mg/L are reported in this series of studies.
- Executive summary:
The acute toxicity of tributylphosphate was investigated in a series of studies in Daphnia magna. 96 -hour EC50 values of between 5 -28.75 mg/L are reported.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published peer reviewed study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- 24-hour acute toxicity to Daphnia magna, using a standardised procedure
- GLP compliance:
- no
- Remarks:
- : literature study
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
No information available. - Analytical monitoring:
- not specified
- Details on sampling:
- No information available.
- Vehicle:
- not specified
- Details on test solutions:
- No information available.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- 24 hour old animals from a clone of Daphnia magna
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 24 h
- Post exposure observation period:
- No information available.
- Hardness:
- 16° (German)
- Test temperature:
- 20°C - 22°C
- pH:
- 7.6 - 7.7
- Dissolved oxygen:
- saturated with oxygen
- Salinity:
- Not relevant
- Nominal and measured concentrations:
- No information available.
- Details on test conditions:
- Tap water free from chlorine
- Reference substance (positive control):
- not specified
- Duration:
- 24 h
- Dose descriptor:
- LC0
- Effect conc.:
- 7 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- 33 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 24 h
- Dose descriptor:
- LC100
- Effect conc.:
- 58 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- No further information available.
- Results with reference substance (positive control):
- No information available.
- Reported statistics and error estimates:
- No information available.
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 24 hour LC50 of tributyl phosphate in Daphnia was 33 mg/L under the conditions of this study.
- Executive summary:
The authors describe the assessment of a number of chemicals in a standardised test for acute toxicity in Daphnia magna. Under the conditions of this assay, the 24 hour EC50 of tributyl phosphate in Daphnia was found to be 33 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 21st June to 25th June 1991
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EPA OTS 795.1200 (Gammarid Acute Toxicity Test)
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- yes
- Details on sampling:
- Tributyl phosphate was measured 48 hours before test initiation and at 0, 48 and 96 hours by gas-liquid chromatography.
Control, vehicle blank and tributyl phosphate-fortified water samples were analysed at each time period. - Vehicle:
- yes
- Details on test solutions:
- A diluted stock solution was prepared at a concentration of 50 mg/ml in dimethyl formamide.
- Test organisms (species):
- Gammarus sp.
- Details on test organisms:
- Gammarus pseudolimnaeus were collected from a spring branch in Missouri and transferred to ABC Laboratories. The spring water in which the gammarids were collected in was gradually diluted with ABC hard-blended test water. The gammarids were housed in glass aquaria, and cultured in aged hard maple leaves, variously under static and flow-through conditions. Temperature of the water was approximately 15-20 °C. The gammarids were fed at least once a week with a suspension of fish food, cereal leaves and alfalfa mixed with algae. They were held under a 16 hour light/8 hour dark photoperiod, with 30 minute dusk and dawn transitions. The organisms were transferred from culture on the day of test initiation. Test organisms were selected from a 17 °C flow-through subculture. Juveniles 2-3mm long were isolated by gently rinsing culture leaves in a glass tray.
- Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- No information provided.
- Hardness:
- 160-190 mg/L hardness as CaCO3
- Test temperature:
- The test chambers were immersed in a water bath maintained at 18 °C ± 2 °C
- pH:
- 8.0-8.2
- Dissolved oxygen:
- 8.0-8.3 mg/L
- Salinity:
- Not relevant
- Nominal and measured concentrations:
- Nominal concentrations: 0.3, 0.6, 1.3, 2.5, and 5.0 mg tributyl phosphate per litre test water.
Mean measured concentrations (gas-liquid chromatography) in filtered samples at 96 hours were: 0.28, 0.52, 1.2, 3.0 and 5.3 mg/L. - Details on test conditions:
- A 0.5 L proportional diluter system with syringe dispenser was used to introduce dilution water and tributyl phosphate compound into test chambers. Flow splitting chambers were used to thoroughly mix and divide each test concentration for delivery to the test chambers. Turbulence was minimised by introducing influent water through 14-gauge needles.
Test chambers consisted of 1 L glass beakers covered with 50 mesh stainless steel screen. A small piece of nylon netting was provided as artificial substrate for the organism.
Dilution water used was ABC hard-blended water, delivered to each test chamber at a rate of ~250 mL/chamber/hour. Alkalinity of dilution water: 182-190 mg/L (as CaCO3). Conductivity of dilution water: 360-370µMhos/cm.
The test system was on a 16 hour light/8 hour dark photoperiod with a 30 minute dusk and dawn transition period. - Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 5.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Remarks:
- (Probit)
- Effect conc.:
- 4.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: 4.0-5.8 mg/L
- Duration:
- 72 h
- Dose descriptor:
- LC50
- Remarks:
- (moving average)
- Effect conc.:
- 2 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: 1.6-2.5 mg/l
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Remarks:
- (moving average)
- Effect conc.:
- 1.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Remarks on result:
- other: 1.4-2.2 mg/L
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 5.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Remarks:
- (Probit method)
- Effect conc.:
- 4.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 4.0-5.8 mg/L
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Remarks:
- (moving average)
- Effect conc.:
- 1.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 1.4-2.2 mg/L
- Duration:
- 96 h
- Dose descriptor:
- EC50
- Remarks:
- (Binomial method)
- Effect conc.:
- 1.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 1.2-3.0 mg/L
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.52 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- other: all effects
- Details on results:
- Abnormal effecs of mortality, lethargy, quiescence, immobility, and/or organisms tending to the bottom of the test chamber were observed in the 1.2, 3.0 and 5.3 mg/L test levels.
- Results with reference substance (positive control):
- Not reported
- Reported statistics and error estimates:
- LC50 values and 95% confidence limits calculated by using the binomial, moving average and probit tests, where data permitted.
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 96 hour EC50 and LC50 values for tributyl phosphate for Gammarus pseudolimnaeus were calculated to be 1.7 mg/L. The 96 hour NOEC was found to be 0.52 mg/L.
- Executive summary:
The acute toxicity of tributyl phosphate to Gammarus pseudolimneaus was determined in a flow through test with duplicate nominal test concentrations of 0.3, 0.6, 1.3, 2.5, and 5.0 mg/L. Abnormal effecs of mortality, lethargy, quiescence, immobility, and/or organisms tending to the bottom of the test chamber were observed in the 1.2, 3.0, and 5.3 mg/L test levels. The 96 hour EC50 and LC50 values for tributyl phosphate for Gammarus pseudolimnaeus were calculated to be 1.7 mg/L. The 96 hour NOEC was found to be 0.52 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published peer reviewed study
- Qualifier:
- according to guideline
- Guideline:
- other: ISO 1975
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- not specified
- Details on sampling:
- No details provided
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna neonates
- Test type:
- not specified
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- Nominal
- Details on test conditions:
- No further information available
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 12.8 mg/L
- Nominal / measured:
- nominal
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 3.65 mg/L
- Nominal / measured:
- nominal
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 2.1 mg/L
- Nominal / measured:
- nominal
- Details on results:
- No further information
- Results with reference substance (positive control):
- Not relevant
- Reported statistics and error estimates:
- No information available
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The 24 hour EC50 of tributyl phosphate in Daphnia was 12.8mg/l.
- Executive summary:
The 24 hour EC50 of tributyl phosphate in Daphnia was 12.8 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Daphnia acute toxicity
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- not specified
- Details on sampling:
- No information available
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna
- Test type:
- not specified
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 24 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- Nominal (assumed; no information available)
- Details on test conditions:
- No information available
- Reference substance (positive control):
- not specified
- Duration:
- 6 h
- Dose descriptor:
- EC50
- Effect conc.:
- 52 mg/L
- Nominal / measured:
- nominal
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 35 mg/L
- Nominal / measured:
- nominal
- Details on results:
- No further information available
- Results with reference substance (positive control):
- No information available
- Reported statistics and error estimates:
- No information available
- Conclusions:
- The 6 hour EC50 of tributyl phosphate in Daphnia was 52mg/l, and the 24 hour EC50 was 35mg/l.
- Executive summary:
The 6 hour EC50of tributyl phosphate inDaphniawas 52 mg/L, and the 24 hour EC50was 35 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Daphnia acute toxicity
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- not specified
- Details on sampling:
- No information available
- Vehicle:
- not specified
- Details on test solutions:
- No information available
- Test organisms (species):
- Daphnia pulex
- Details on test organisms:
- Daphnia pulex
- Test type:
- not specified
- Water media type:
- not specified
- Limit test:
- no
- Total exposure duration:
- 24 h
- Post exposure observation period:
- No information available
- Hardness:
- No information available
- Test temperature:
- No information available
- pH:
- No information available
- Dissolved oxygen:
- No information available
- Salinity:
- No information available
- Nominal and measured concentrations:
- Nominal (assumed; no information available)
- Details on test conditions:
- No information available
- Reference substance (positive control):
- not specified
- Duration:
- 6 h
- Dose descriptor:
- EC50
- Effect conc.:
- 93 mg/L
- Nominal / measured:
- nominal
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 68 mg/L
- Nominal / measured:
- nominal
- Details on results:
- No further information available
- Results with reference substance (positive control):
- No information available
- Reported statistics and error estimates:
- No information available
- Conclusions:
- The 6 hour EC50 of tributyl phosphate in Daphnia pulex was 93mg/l, and the 24 hour EC50 was 68mg/l.
- Executive summary:
The 6-hour EC50of tributyl phosphate in Daphnia pulex was 93 mg/L, and the 24 hour EC50was 68 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published literature study
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Assessmnet of acute aquatic toxicity using Moina macrocopa
- GLP compliance:
- no
- Remarks:
- : literature study
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not relevant - Analytical monitoring:
- yes
- Details on sampling:
- no data
- Vehicle:
- yes
- Details on test solutions:
- A supersaturated solution of a chemical was agitated for 2 hours at over 20 °C and left for 2 hours at 20 ° C in order to determine solubility. The water phase was filtered with filter paper for analysis. The no-octanol/water partition coefficient was determined by dissolving a chemical in distilled water at a concentration of 1-4 mol/L. n-Octanol or water, respectively, was added so that the ratio of n-octanol/water was 0.2 and it was agitated at 20 °C or 2 hours. Both phases, were then separated and filtered for analysis. The concentration of the chemical in the water and n-octanol phases was determined by gas chromatography with a 3-m x 2-mm glass column or by ultraviolet spectrophotometry.
- Test organisms (species):
- other: Moina macrocopa
- Details on test organisms:
- The culture medium for breeding Moina macrocopa was prepared by mixing liquids A and B in the ratio of 9:1, and was neutralised by NaHCO3 before use. Liquid A was prepared by boiling 1 L of distilled water with 4 g of rice straw for 2 hours, and after filtration it was left for 24 hours to increase bacteria. Liquid B was a soil extract prepared by the same method as the liquid A. Moina macrocopa was cultured in the medium, and those of about 5 days old were used.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Post exposure observation period:
- No data
- Hardness:
- No information provided
- Test temperature:
- 20 ± 1 °C
- pH:
- No information provided
- Dissolved oxygen:
- No information provided
- Salinity:
- No information provided
- Nominal and measured concentrations:
- No information provided
- Details on test conditions:
- The culture medium for breeding Moina macrocopa was prepared by mixing liquids A and B in the ratio of 9:1, and was neutralised by NaHCO3 before use. Liquid A was prepared by boiling 1 L of distilled water with 4 g of rice straw for 2 hours, and after filtration it was left for 24 hours to increase bacteria. Liquid B was a soil extract prepared by the same method as the liquid A. Moina macrocopa was cultured in the medium, and those of about 5 days old were used. Ten Moina macrocopa in 100 mL of test solution was put in a 250 mL vail vessel at 20 ± 1 °C and the survivors were counted after 3 hours of exposure to determien the LC50.
- Reference substance (positive control):
- not specified
- Duration:
- 3 h
- Dose descriptor:
- LC50
- Effect conc.:
- 1.8 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Details on results:
- No further details on the results
- Results with reference substance (positive control):
- Not relevant
- Reported statistics and error estimates:
- No information provided
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The LC50 of the test material in Moina macropopa was found to be 1.8 mg/L.
- Executive summary:
The authors describe an assay to assess the acute toxicity of chemicals to the cladoceran, Moina macrocopa. The 3 -hour LC50 of tributylphosphate was found to be 1.8 mg/L.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Published study
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The authors describe a method to assess the acute toxicity of chemicals to the flatworm, Dugesia japonica
- GLP compliance:
- no
- Remarks:
- : published study
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material:
Not applicable - Analytical monitoring:
- yes
- Details on sampling:
- No data
- Vehicle:
- yes
- Details on test solutions:
- A supersaturated solution of a chemical was agitated for 2 hours at over 20 °C and left for 2 hours at 20 ° C in order to determine solubility. The water phase was filtered with filter paper for analysis. The no-octanol/water partition coefficient was determined by dissolving a chemical in distilled water at a concentration of 1-4 mol/L. n-Octanol or water, respectively, was added so that the ratio of n-octanol/water was 0.2 and it was agitated at 20 °C or 2 hours. Both phases, were then separated and filtered for analysis. The concentration of the chemical in the water and n-octanol phases was determined by gas chromatography with a 3-m x 2-mm glass column or by ultraviolet spectrophotometry.
- Test organisms (species):
- other aquatic worm: Dugesia japonica
- Details on test organisms:
- The breeding liquid for Dugesia japonica was prepared bu dissolving 3.74 g of NaCl, 0.49 g KCL and 8.55 g of CaCl2 into distilled water to make 500 mL. This was diluted 100 times and neutralised by NaHCO3 befoer use. Dugesia japonica were collected from a stream around which there was no source of pollution and left with-out food for over 7 days in the breeding liquid to excrete alimentary canal contents. Those of about 2 cm long were used. Dugesia japonica was cut into two parts at the nearest section to the eyes of the trisected part between pharnyx and eyes. The body part was used for the regeneration test.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 7 d
- Post exposure observation period:
- No information provided
- Hardness:
- No information provided
- Test temperature:
- No information provided
- pH:
- No information provided
- Dissolved oxygen:
- No information provided
- Salinity:
- No information provided
- Nominal and measured concentrations:
- No information provided
- Details on test conditions:
- Test species of about 2 cm long were used. Dugesia japonica was cut into two parts at the nearest section to the eyes of the trisected part between pharnyx and eyes. The body part was used for the regeneration test. Ten body parts were put in 100 mL of a test solution, and this was left at 20 ± 1 °C for 7 days. Observation for head regeneration was carried out with a stereomicroscope on Days 3, 4, 5, 6 and 7 after head cutting, and the test solution was replaced at every observation.
- Reference substance (positive control):
- not specified
- Duration:
- 7 d
- Dose descriptor:
- LC50
- Effect conc.:
- 1 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 7 d
- Dose descriptor:
- EC50
- Effect conc.:
- 0.6 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- test mat.
- Details on results:
- No further information provided
- Results with reference substance (positive control):
- Not relevant
- Reported statistics and error estimates:
- No information provided
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The LC50 was found to be 1.0 mg/L; the EC50 for head regeneration was found to be 0.6 mg/L.
- Executive summary:
The authors describe a method for assessing the acute toxicity of chemicals to the flatworm, Dugesia japonica. Organisms were exposed for 7 days and mortality and head regeneration assessed. Unde the conditions of this assay, the LC50 for tributylphosphate was found to be 1.0 mg/L; the EC50 for head regeneration was found to be 0.6 mg/L.
Referenceopen allclose all
The 96-hour NOEC of tributyl phosphate to the Gammarid Hyalella azteca was < 1.9 mg/L, and the 96 hour LC50 was 2.4 mg/L.
The 48 -hour EC50 of tributyl phosphate in Daphnia was 2.6 mg/L.
The 48-hour NOEC of tributyl phosphate in Daphnia magna was 1.8 mg/L.
The 24-hour EC50 value for tributyl phosphate in Daphnia is 30 mg/L.
EC50 values of between 5 -28.75 mg/L are reported in this series of studies.
The 24 hour LC50 of tributyl phosphate in Daphnia magna was 33 mg/L under the conditions of this study.
The 96 hour EC50 and LC50 values for tributyl phosphate for Gammarus pseudolimnaeus were calculated to be 1.7 mg/L. The 96 hour NOEC was found to be 0.52 mg/L.
The 24 hour EC50 of tributyl phosphate in Daphnia magna was 12.8 mg/L.
The 6 hour EC50 of tributyl phosphate in Daphnia was 52 mg/L, and the 24 hour EC50 was 35 mg/L.
The 6-hour EC50 of tributyl phosphate in Daphnia pulex was 93 mg/L, and the 24 hour EC50 was 68 mg/L.
The LC50 of the test material in Moina macropopa was found to be 1.8 mg/L.
The LC50 was found to be 1.0 mg/L; the EC50 for head regeneration was found to be 0.6 mg/L.
Description of key information
A large number of studies, performed in a number of species, are available.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- 1.8 mg/L
Additional information
The results of a large number of studies are available and are sumamrised below. In addition, the range-finding study for the 21 -day reproduction test, Kuehn et al (1989) reports 24 -hour LC0 and LC50 values for tributylphosphate in Daphnia magna of 9.3 and 35 mg/L respectively.
The lowest EC50-value reported by England & Cramer (1991, guideline study, reliability 1, LoA) was not chosen as key value for chemical safety assessment due to the fact that Gammarus pseudolimnaeus is not a standard test organism as advised in the OECD testing guidelines. The lowest and thus most conservative LC50 value for the standard organism Daphnia magna (ABC Laboratories, 1978, 48h-LC50: 1.8 mg/L) was chosen instead.
Species | EC50 (mg/L) | Time (h) | Reference |
Daphnia magna | 30 | 96 | Bringmann & Kuehn, 1982 |
Daphnia magna | 5-28.75 | 96 | Bayer, 1985 |
Daphnia magna | 33 | 24 | Bringmann & Kuehn, 1977 |
Gammarus pseudolimnaeus | 1.7 | 96 | England & Cramer, 1991 |
Daphnia magna | 12.8 | 24 | Dave et al, 1981 |
Daphnia magna | 1.8 | 48 | ABC Laboratories, 1978 |
Daphnia magna | 52 | 6 | Wakabayashi et al, 1988 |
35 | 24 | ||
Daphnia magna | 2.6 | 48 | ABC Laboratories, 1990 |
Daphnia pulex | 6 | 93 | Wakabayashi et al, 1988 |
24 | 68 | ||
Hyalella azteca | 2.4 | 96 | England & Schrier, 1990 |
Moina macrocopa | 1.8 | 3 | Yoshioda et al, 1986 |
Dugesia japonica | 1.3 | 3 |
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