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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
Partition coefficient
Administrative data
- Endpoint:
- partition coefficient
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1969
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 970
- Report date:
- 1969
Materials and methods
- Principles of method if other than guideline:
- yridamole, European J. Pharmacoi. 9 (1970) 265-268.
14C_labele d adenosine, inosine, adenine, hypoxanthine, uric acid or ribose were added at a dose of 0.004 umoles
to the perfusion fluid of isolated guinea-pig hearts. During a single passage through the heart, 30% of adenosine and
18% of inosine, but only 7% of adenine, 4.5% of hypoxanthine, 2% of uric acid and 2% of ribose was taken up.
Dipyridamole in a concentration of 10 -s M reduced the uptake of adenosine and inosine by 50%, but the uptake of
adenine, hypoxanthine, uric acid and ribose was not affected by dipyridamole, even with concentrations of 10 -s M.
Furthermore, the uptake of adenosine was inh~ited by inosine, but not by adenine or by hypoxanthine.
The octanol/water distribution of the compounds was studied to detect any influence of the degree of lipophilia
of each substance on its uptake by the heart. Of the following pairs of purine derivatives, adenosine : inosine and
adenine : hypoxanthine, the compound better taken up by the heart was also the more lipophilic of each pair.
However, the presence of ribose in the chemical structure appears to be of greater importance quantitatively in
determining the myocardial uptake of the purine derivatives. - GLP compliance:
- no
- Type of method:
- estimation method (solubility ratio)
- Partition coefficient type:
- octanol-water
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
Study design
- Analytical method:
- other: 14C count
Results and discussion
Partition coefficient
- Key result
- Type:
- log Pow
- Partition coefficient:
- ca. -2.32
- Temp.:
- 20 °C
- pH:
- ca. 7.4
Applicant's summary and conclusion
- Conclusions:
- Log Kow of D-Ribose at pH 7.4 is -2.32
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