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EC number: 222-294-1 | CAS number: 3407-42-9
- 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 microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms, other
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Remarks:
- Experimental data of various test chemicals
- Justification for type of information:
- Data for the target chemical is from collection of data
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- other: Refer below principle
- Principles of method if other than guideline:
- WoE report is based on toxicity study of microorganism for the test chemical:
WoE 2 and 3rd - GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- other: S. aureus, B. cereus , E. coli , P. aeruginosa
- Test type:
- static
- Water media type:
- freshwater
- Total exposure duration:
- 48 h
- Details on test conditions:
- 2nd and 3rd study:
Test vessel: Petri plate
-The turbidity of microorganisms was adjusted to 0.5 McFarland. The inoculum were 1×108 1×106 CFU/ml for bacteria and fungi respectively. Inoculate was wabbed on Muller Hinton Agar.Sterile blank discs impregnated with 3, 5, 10 μl of oil in 10 μl of dimethyl sulfoxide (DMSO) were used and put on cultured plates. - Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- other: MIC
- Effect conc.:
- > 8 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: 2nd study
- Duration:
- 48 h
- Dose descriptor:
- other: MIC
- Effect conc.:
- 1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Remarks on result:
- other: 3rd study
- Validity criteria fulfilled:
- no
- Conclusions:
- The test chemical is likely to be toxic to microorganism atleast in the concentartion range of 1 to 8 mg/l.
- Executive summary:
Data available for the test chemicals has been reviewed to determine its effect on microoranism.The studies are as mentioned below:
In the first study toxicity of test material was evaluated for microorganisms by disc diffusion method and the minimum inhibition concentration was evaluated using broth dilution method. The organisms used for the test were S. aureus, B. cereus , E. coli , P. aeruginosa. The turbidity of microorganisms was adjusted to 0.5 McFarland. The inoculum were 1×1081×106CFU/ml for bacteria and fungi respectively. Inoculate was swabbed on Muller Hinton Agar. Sterile blank discs impregnated with 3, 5, 10 μl of oil in 10 μl of dimethyl sulfoxide (DMSO) were used and put on cultured plates. Disc containing DMSO and antibiotics were used as control. The minimum inhibition concentration of test material on bacteria S. aureus, B. cereus , E. coli , P. aeruginosa was observed to be > 8 mg/l.
Above study was supported by the second from secondary source. Toxicity of test material was evaluated for microorganisms by disc diffusion method and the minimum inhibition concentration was evaluated using broth dilution method. The organisms used for the test were S. aureus, B. cereus , E. coli , P. aeruginosa. The turbidity of microorganisms was adjusted to 0.5 McFarland. The inoculum were 1×1081×106CFU/ml for bacteria and fungi respectively. Inoculate was swabbed on Muller Hinton Agar. Sterile blank discs impregnated with 3, 5, 10 μl of oil in 10 μl of dimethyl sulfoxide (DMSO) were used and put on cultured plates. Disc containing DMSO and antibiotics were used as control. The minimum inhibition concentration of test material on bacteria S. aureus, B. cereus , E. coli , P. aeruginosa was observed to be 1 mg/l.
The test chemical is likely to be toxic to microorganism atleast in the concentartion range of 1 to 8 mg/l.
Reference
Description of key information
The test chemical is likely to be toxic to microorganism atleast in the concentartion range of 1 to 8 mg/l.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 mg/L
Additional information
Data available for the test chemicals has been reviewed to determine its effect on microoranism.The studies are as mentioned below:
In the first study toxicity of test material was evaluated for microorganisms by disc diffusion method and the minimum inhibition concentration was evaluated using broth dilution method. The organisms used for the test were S. aureus, B. cereus , E. coli , P. aeruginosa. The turbidity of microorganisms was adjusted to 0.5. The inoculum were 1×1081×106CFU/ml for bacteria and fungi respectively. Inoculate was swabbed on Muller Hinton Agar. Sterile blank discs impregnated with 3, 5, 10 μl of oil in 10 μl of dimethyl sulfoxide (DMSO) were used and put on cultured plates. Disc containing DMSO and antibiotics were used as control. The minimum inhibition concentration of test material on bacteria S. aureus, B. cereus , E. coli , P. aeruginosa was observed to be > 8 mg/l.
Above study was supported by the second from secondary source. Toxicity of test material was evaluated for microorganisms by disc diffusion method and the minimum inhibition concentration was evaluated using broth dilution method. The organisms used for the test were S. aureus, B. cereus , E. coli , P. aeruginosa. The turbidity of microorganisms was adjusted to 0.5. The inoculum were 1×1081×106CFU/ml for bacteria and fungi respectively. Inoculate was swabbed on Muller Hinton Agar. Sterile blank discs impregnated with 3, 5, 10 μl of oil in 10 μl of dimethyl sulfoxide (DMSO) were used and put on cultured plates. Disc containing DMSO and antibiotics were used as control. The minimum inhibition concentration of test material on bacteria S. aureus, B. cereus , E. coli , P. aeruginosa was observed to be 1 mg/l.
The test chemical is likely to be toxic to microorganism atleast in the concentartion range of 1 to 8 mg/l.
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