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EC number: 274-357-8 | CAS number: 70161-44-3
- 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
Toxicity to birds
Administrative data
- Endpoint:
- short-term toxicity to birds: acute oral toxicity test
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study according to a FIFRA guideline.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 991
- Report date:
- 1991
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EPA OPP 71-1 (Avian Acute Oral Toxicity Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Sodium N-(hydroxymethyl)glycinate
- EC Number:
- 274-357-8
- EC Name:
- Sodium N-(hydroxymethyl)glycinate
- Cas Number:
- 70161-44-3
- Molecular formula:
- C3H7NO3.Na
- IUPAC Name:
- sodium N-(hydroxymethyl)glycinate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- Suttocide A (Powder}; Lot No. J15-150D with a purity of 97%.
Constituent 1
- Dose method:
- other: a single dose of the test substance in diluent was orally intubated directly into the crop or proventriculus of each bird using a stainless steel cannula.
- Analytical monitoring:
- yes
- Vehicle:
- yes
Test organisms
- Test organisms (species):
- Colinus virginianus
Study design
- Limit test:
- no
- Remarks:
- 1. Acclimation - 16 days. 2. Fasting - At least 15 hours prior to dosing. 3. Dosing - Experimental Start Date - October 12, 1990. 4. Post-dosing observation - 14 days.
- No. of animals per sex per dose and/or stage:
- 5
- Control animals:
- yes
Results and discussion
Effect levels
- Duration (if not single dose):
- 14 d
- Dose descriptor:
- LD50
- Effect level:
- > 2 250 mg/kg bw
- Conc. / dose based on:
- test mat.
- Basis for effect:
- mortality
Any other information on results incl. tables
There were no mortalities at the 486, 810 or 1350 mg/kg dosages. There was a single, incidental mortality at 292 mg/kg. There was 40% mortality (4 of 10) at 2250 mg/kg. Treatment related effectswere seen at 810 mg/kg and higher dosages. These effects were reversible even at the highest dosage. Signs of toxicity typical of intoxication with Suttocide A included ruffled appearance, lethargy, reduced reaction to external stimuli (sound and movement), lower limb weakness, depression, wing droop and coma.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The acute oral LD5O value for northern bobwhite exposed to Suttocide A as a single oral dosage was determined to be greater than 2250 mg/kg, the highest dosage tested. The no mortality level was 1350 mg/kg. The no observed effect level was 486 mg/kg based on signs of toxicity and a loss in body weight at 810 mg/kg.
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