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EC number: 200-059-4 | CAS number: 50-69-1
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2018/2019
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 019
- Report date:
- 2019
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- D-ribose
- EC Number:
- 200-059-4
- EC Name:
- D-ribose
- Cas Number:
- 50-69-1
- Molecular formula:
- C5H10O5
- IUPAC Name:
- D-ribose
- Test material form:
- solid: particulate/powder
- Details on test material:
- Dry powder, white to slightly yellow
Constituent 1
- Specific details on test material used for the study:
- Appearance: White to slightly yellow powder
Batch: Q0926501
Purity/Composition: 99.3%
Test item storage: At room temperature protected from light
Stable under storage conditions until: 30 November 2019 (expiry date)
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- Frequency: at t=0 h and t=48 h.
Volume: 40 mL from the approximate centre of the test vessels.
Storage: Samples were stored in a refrigerator (2-8°C) until analysis.
Test solutions
- Details on test solutions:
- The batch of D-ribose tested was a white to slightly yellow powder with a purity of 99.3% and completely soluble in test medium at the solutions prepared. No correction was made for the purity/composition of the test item.
Preparation of test solutions started with the highest concentration of 100 mg/L in the range-finding test and a stock solution of 1000 mg/L in the limit test applying a 10-15 minute period of magnetic stirring to accelerate dissolution of the test item in medium. Lower test concentrations were prepared by subsequent dilutions of the highest concentration or stock solution in test medium. All test solutions were clear and colorless at the end of the preparation procedure.
Any residual volumes were discarded.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- * Species: Daphnia magna (Crustacea, Cladocera) (Straus, 1820), at least third generation, obtained by a cyclical parthenogenesis under specified breeding conditions.
* Source: In-house laboratory culture with a known history.
* Reason for selection: This system has been selected as an internationally accepted invertebrate species.
* Validity of batch Daphnids originated from a healthy stock, 2nd to 5th brood, showing no signs of stress such as mortality >20%, presence of males, ephippia or discoloured animals and there was no delay in the production of the first brood.
* Characteristics: Daphnia, less than 24 hours old, from parental daphnids of more than two weeks old.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Test temperature:
- The temperature continuously measured in a temperature control vessel varied between 20 and 21°C during the test, and complied with the requirements as laid down in the study plan (18-22°C, constant within ±1°C).
- pH:
- pH was only measured in the control and the highest test concentration.
pH was:
- for control: 7.6 at t=0h and 8.1 at t=48h
- for highest test concentration (i.e. 100 nominal concentration mg/L): 7.7 at t=0h and 8.1 at t=48h - Dissolved oxygen:
- Dissolved oxygen concentrations was only measured in the control and the highest test concentration.
Dissolved oxygen was:
- for control: 8.9 mg/L at t=0h and 8.8 mg/L at t=48h
- for highest test concentration (i.e. 100 nominal concentration mg/L): 9.0 mg/L at t=0h and 8.7 mg/L at t=48h - Nominal and measured concentrations:
- Measured concentration reached 96 to 98% of nominal concentration.
- Details on test conditions:
- A range-finding test was performed to provide information about the range of concentrations to be used in the final test. Test procedure and conditions were similar to those applied in the limit test with the following exceptions:
- Ten daphnids per concentration (in duplicate, 5 per vessel) were exposed to a range of 0.10 to 100 mg/L increasing by a factor of 10 and to a control.
- Dissolved oxygen concentrations and pH were only measured in the control and the highest test concentration.
- No sampling for determination of actual exposure concentrations was performed. - Reference substance (positive control):
- no
Results and discussion
Effect concentrations
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- No immobility was observed in the control or in the limit concentration throughout the exposure period. The responses recorded in this test allowed for reliable determination of an EC50 and were in agreement with what was expected based on the results of the range-finding test.
At the start and end of the test, the carbon concentration observed at the limit concentration was comparable to the expected nominal carbon concentration of 40 mg/L. The carbon concentration measured in the limit concentration of 100 mg/L remained stable during the test period, i.e. was 94% of the initially measured concentration.
Any other information on results incl. tables
A sample taken from the 1000 mg/L stock solution was analysed. The measured concentration was 98% of nominal at the start of the test and thus confirmed correct preparation of the test solution.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- No immobility was observed in the control or any of the concentrations tested throughout the test.
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