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Diss Factsheets
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EC number: 215-925-7 | CAS number: 1453-58-3
- 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
Field studies
Administrative data
- Endpoint:
- field studies accumulation
- Remarks:
- Residues in plants
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1982-1983
- 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:
- study report
- Title:
- Unnamed
- Year:
- 1 984
- Report date:
- 1984
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- GLP compliance:
- no
- Media:
- water, plants, soil
Test material
- Reference substance name:
- 3-methylpyrazole
- EC Number:
- 215-925-7
- EC Name:
- 3-methylpyrazole
- Cas Number:
- 1453-58-3
- Molecular formula:
- C4H6N2
- IUPAC Name:
- 3-methyl-1H-pyrazole
- Test material form:
- liquid
Constituent 1
Results and discussion
Applicant's summary and conclusion
- Conclusions:
- The parent compound CMP is taken up by the plant and converted within a few days.
3-methypyrazole was isolated and identified as the conversion product. A similar finding was also obtained from the investigations in the soil.
Since CMP residues are not to be expected on the basis of these results, all further residue-toxicological investigations were continued with the transformation product 3-MP.
According to the uptake and transport studies, the MP is taken up by the plant via leaf and root.
In two vegetation periods and at different locations, residue dynamic investigations and residue determinations were carried out on samples from plot trials with application rates of 2 to 8 kg active substance/ha 1, after autumn and spring application of CMP.
No free 3-MP was detected in the cereal grain at harvest (<0.03 ppm). This also applied to the other substrates straw and beet, where, however, residues of up to 0.1 ppm were found in a few exceptions.
Translated with www.DeepL.com/Translator (free version) - Executive summary:
The parent compound CMP is taken up by the plant and converted within a few days.
3-methypyrazole was isolated and identified as the conversion product. A similar finding was also obtained from the investigations in the soil.
Since CMP residues are not to be expected on the basis of these results, all further residue-toxicological investigations were continued with the transformation product 3-MP.
According to the uptake and transport studies, the MP is taken up by the plant via leaf and root.
In two vegetation periods and at different locations, residue dynamic investigations and residue determinations were carried out on samples from plot trials with application rates of 2 to 8 kg active substance/ha 1, after autumn and spring application of CMP.
No free 3-MP was detected in the cereal grain at harvest (<0.03 ppm). This also applied to the other substrates straw and beet, where, however, residues of up to 0.1 ppm were found in a few exceptions.Translated with www.DeepL.com/Translator (free version)
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