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EC number: 203-509-8 | CAS number: 107-66-4
- 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:
- 10/1992
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- Origin: West-Aquarium (Bad Lauterberg)
Body length: 2.5 - 3.5 cm
mortality during cultivation: < 2 %
keeping water: synthetic fresh water in arccordance with ISO - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- 10.9 °dH
- Test temperature:
- 20.9 - 21.4°C
- pH:
- 7.2 - 8.2
- Dissolved oxygen:
- 7.8 - 9.1 (90.5 - 104.2%)
- Nominal and measured concentrations:
- Nominal conc: 100 mg/L (direct weight)
- Details on test conditions:
- - Test aquarium: 300*135*200 mm
- 5 l Test medium with air circulation
- 16 hour light and 8 hour dark
- Amount of fish per test vessel: 10 - Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Sublethal observations / clinical signs:
Application of test substance: direct weighing.
Undissolved particles of test substance sedimented on the ground of the vessel, but were dissolved after 15 minutes.
- Validity criteria fulfilled:
- yes
- Remarks:
- No mortality in the control was observed. The dissolved oxygen concentration remained above 90% throughout the exposure period.
- Conclusions:
- The acute toxicity of dibutyl hydrogen phosphate to fish was conducted in a static test according to EU Method C.1 (Acute Toxicity for Fish). After 96 hours of exposure a LC0 value of ≥ 100 mg/L was obtained.
- Executive summary:
The acute toxicity of dibutyl hydrogen phosphate to fish was conducted in a static test according to EU Method C.1 (Acute Toxicity for Fish). After 96 hours of exposure a LC0 value of ≥ 100 mg/L was obtained. The reported value related to nominal concentration.
Reference
Description of key information
The acute toxicity of dibutyl hydrogen phosphate to fish was conducted in a static test according to EU Method C.1 (Acute Toxicity for Fish). After 96 hours of exposure a LC0 value of ≥ 100 mg/L was obtained.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Dose descriptor:
- EC50
- Effect concentration:
- > 100 mg/L
Additional information
For dibutyl hydrogen phosphate two reliable studies on acute toxicity to Danio rerio are available, showing no acute effects of dibutyl hydrogen phosphate towards fish.
The acute toxicity of dibutyl hydrogen phosphate to Danio rerio was conducted in a static limit test according to EU Method C.1 (Acute Toxicity for Fish). After 96 hours of exposure a LC0 value of ≥ 100 mg/L was obtained. The reported value related to nominal concentration, as no analytical monitoring was carried out.
In a second experiment, fish were exposed to dibutyl hydrogen phosphate at concentrations of 5000, 7071 and 10000 mg/l under static conditions.
According to the method "Letale Wirkung beim Zebrabaerling (Brachydanio rerio new name: Danio rerio) LC0 / LC50 / LC 100 nach 48 - 96 Stunden" (Umweltbundesamt Berlin, Stand: Mai 1984), a 96h-LC0 of >= 10000 mg/L was received on Brachydanio rerio (new name: Danio rerio). The value is given as nominal concentration as measured concentrations determined via NMR spectroscopy differ less than 5.4 % from nominal concentrations.The substance concentrations were confirmed by analytical monitoring.
Further, a lower value on toxicity of dibutyl hydrogen phosphate to fish was found for the species Oryzias latipes. A 96h-LC50 of 110 mg/l conducted according to OECD TG 204 by the National Institute of Technology and Evaluation, Japan, is reported. The study is not taken into account for assessment, based on the following reason:
Dibutyl hydrogen phosphate was assessed within the scope of the ICCA/HPV-program. Preparing the OECD SIDS-dossiers the studies conducted by the National Institute of Technology and Evaluation, Japan were not available. Information on study design and results are only presented in the OECD-SIDS Report and the OECD-SIDS dossier. In the OECD-SIDS report, the composition of the assessed substance is reported to be a mixture of 64% dibutyl phosphate, 20% tributyl phosphate and 16% monobutyl phosphate. In the context of REACH, the assessed substance/mixture would be regarded as a multi-constituent substance. In the OECD-SIDS dossier, it is reported that dibutyl phosphate with a purity of 97.6% was used as test substance in ecotoxicity tests. It is not really clear, if the degree of purity refers to pure dibutyl hydrogen phosphate or to the assessed substance, which under REACH would be regarded as a multi-constituent substance. Therefore, it is concluded that sameness of both substances, the assessed substance within the OECD-SIDS dossiers and the substance to be registered cannot be proved/demonstrated. The studies conducted by the National Institute of Technology and Evaluation, Japan are considered to be reliable, but they are not taken into account for assessment, based on lack of clarity on substance sameness.
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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