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Diss Factsheets
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EC number: 203-117-7 | CAS number: 103-49-1
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1994-11-29 tol 1994-11-30
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- Principles of method if other than guideline:
- A defined amount of activated sludge is mixed with synthetic medium and measured the rate of respiration. This respiration rate is compared with those in the test preparations with different concentrations of the test substance be measured. The sensitivity of the activated sludge is examined with 3.5-dichlorophenol as a reference.
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Details on sampling:
- - Test concentrations: 100, 180, 320, 560 and 1000 mg/L
- Control concentration: 10000 mg/L - Vehicle:
- no
- Test organisms (species):
- activated sludge, domestic
- Details on inoculum:
- - Type: activated suldge (mixed population various microorganisms)
- Origin: Laboratory sewage treatment plant, which is operated with synthetic (the municipal wastewater approximate) growth medium.
- Prepreration: no
- pH of the culture solution before depletion: 7.9 - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 30 min
- pH:
- 20 ± 2 °C
- Details on test conditions:
- - direct weighing
- Concentration of activated sludge in the test system: 800.0 mg/L
- Contact time / duration: 30 min. under continuous aeration - Reference substance (positive control):
- yes
- Remarks:
- 3.5-Dichlorphenol
- Key result
- Duration:
- 30 min
- Dose descriptor:
- EC50
- Effect conc.:
- 171 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Details on results:
- Prüfkonzentration Respirationsrate Hemmung
[mg/L] [mg/L x h] [%]
100 28.3 32.9
180 22.3 47.2
320 11.1 73.7
560 4.8 88.6
1000 3.0 92.9
Control 42.2 - Results with reference substance (positive control):
- The sensitivity of the activated sludge was the reference substance 3,5-dichlorophenol reviewed. For 3,5-dichlorophenol, an EC 50 value of
12.0 mg/L determined graphically. - Validity criteria fulfilled:
- yes
- Conclusions:
- An activated sludge respiration inhibition test (according to OECD guideline 209) with activated sludge resulted in a 30 min EC50 = 171 mg/L.
- Executive summary:
The potential toxicity of dibenzylamine to microorganisms was tested according to EU Method C.11 (1994), which is equal to OECD Guideline 209. Toxicity to microorganisms of dibenzylamine was determined as EC50 = 171 mg/L after 30 minutes exposure.
Reference
Description of key information
The study of Bayer (1995), investigating the toxicity of dibenzylamine to microorganisms according to OECD guideline 209, was considered as the key study for endpoint coverage (Klimisch score of 2). The 30 min EC50 was 171 mg/L.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 171 mg/L
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.