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EC number: 229-662-0 | CAS number: 6642-31-5
- 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
Vapour pressure
Administrative data
Link to relevant study record(s)
- Endpoint:
- vapour pressure
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- until 2002-07-19
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.4 (Vapour Pressure)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- other: The melting point of 1,3-DIMETHYL-4-AMINOURACIL was determined. Using the estimated boiling point of 1.3-DIMETHYL-4-AMINOURACIL, the vapour pressure was calculated using the Modified Watson Correlation.
- Specific details on test material used for the study:
- Colour: White
Aggregate State at Room Temperature: Solid
Molecular Weight: 155.16 g/mol
Molecular Formula: C6H9N3O2 - Key result
- Temp.:
- 25 °C
- Vapour pressure:
- 0 Pa
- Conclusions:
- The GLP study was performed according to the EEC directive 92/69, Part A, Methods for the determination of physico-chemical properties, A.4 "Vapour Pressure", EEC Publication No. L383, December 1992 and the OECD Guideline No. 104, "Vapour Pressure", adopted July 27, 1995.
The vapour pressure of the test substance was estimated to be 1.0 x 10E-7 Pa. This procedure is considered scientifically reasonable as is supported by the requirements under REACH: "The study does not need to be conducted if the melting point is above 300 °C. If the melting point is between 200 °C and 300 °C, a limit value based on measurement or a recognised calculation method is sufficient." - Executive summary:
The GLP study was performed according to the EEC directive 92/69, Part A, Methods for the determination of physico-chemical properties, A.4 "Vapour Pressure", EEC Publication No. L383, December 1992 and the OECD Guideline No. 104, "Vapour Pressure", adopted July 27, 1995.
The boiling point of 1.3-DIMETHYL-4-AMINOURACIL was estimated to be above 400 °C. The melting point of the substance was determined to be 299 °C. A temperature range up to 400 °C was tested. In this temperature range no boiling of 1.3-DIMETHYL-4-AMINOURACIL was observed. Therefore it was supposed, that the boiling point of 1,3-DIMETHYL-4-AMINOURACIL is above 400 °C. For the calculation of the vapour pressure a estimated boiling point of 400 °C was used.The vapour pressure of the test substance was estimated to be 1.0 x 10E-7 Pa at 25 °C based on the estimated boiling point of 400°C and using the Modified Watson Correlation.
- Endpoint:
- vapour pressure
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP-guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 104 (Vapour Pressure Curve)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- effusion method: by loss of weight or by trapping vaporisate
- Temp.:
- 20 °C
- Vapour pressure:
- < 0 hPa
- Temp.:
- 50 °C
- Vapour pressure:
- < 0 hPa
Referenceopen allclose all
The boiling point of 1.3-DIMETHYL-4-AMINOURACIL was estimated to be above 400 °C. The melting point of 1.3-DIMETHYL-4-AMINOURACIL was determined to be 299 °C. A temperature range up to 400 °C was tested. In this temperature range no boiling of 1.3-DIMETHYL-4-AMINOURACIL was observed. Therefore it was supposed, that the boiling point of 1,3-DIMETHYL-4-AMINOURACIL is above 400 °C. For the calculation of the vapour pressure a estimated boiling point of 400 °C was used.
Description of key information
Vapour pressure:
< 1 * 10exp(-6) hPa at 20°C resp. 50°C (effusion method: by loss of weight or by trapping vaporisate, OECD 104, GLP)
7.53 * 10exp(-6) mm Hg at 25°C (database entry, QSAR estimation)
1 * 10exp(-7) hPa at 25°C (calculated using the Modified Watson Correlation, OECD 104, GLP)
Key value for chemical safety assessment
- Vapour pressure:
- 0 hPa
- at the temperature of:
- 25 °C
Additional information
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.