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EC number: 204-327-1 | CAS number: 119-47-1
- 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:
- 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- ISO 8192 (Water quality - Test for inhibition of oxygen consumption by activated sludge for carbonaceous and ammonium oxidation)
- GLP compliance:
- no
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material: not reported
- Analytical monitoring:
- no
- Details on sampling:
- not applicable
- Vehicle:
- no
- Details on test solutions:
- 8 mL of the synthetic medium and 25 mL of activated sludge were added to the dissolved test item. The mixture was filled up to 250 mL with water and aerated at 20°C +/-2°C.
The exposure medium with the reference substance was prepared by adding 8 mL of the sythetic medium, 25 mL of activated sludge and a defined amount of the stock solution to achieve the test concentrations and was filled up to 250 mL with water. - Test organisms (species):
- activated sludge
- Details on inoculum:
- Sludge:
The sludge was withdrawn of a laboratory scale sewage treatment unit (3L).
The start concentration of activated sludge was about 6.00 g/L dry matter. The dry matter content of 1 g of wet activated sludge was 0.03 g. Therefore, a required quantity of 400 g/2 L was used in the test.
Synthetic medium:
A synthetic waste water feed was made by dissolving the following amounts of substance in 1 litre of water:
16.0 g peptone
11.0 g meat extract
3.0 g urea
0.7 g NaCl
0.4 g CaCl2 x 2 H2O
0.2 g MgSO4 x 7 H2O
2.8 g K2HPO4 - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Post exposure observation period:
- not reported
- Hardness:
- not reported
- Test temperature:
- 20°C +/- 2°C
- pH:
- Test 1: 7.5-8.2
Test 2: 7.8-8.5 - Dissolved oxygen:
- not reported
- Salinity:
- not reported
- Nominal and measured concentrations:
- Test 1: nominal concentrations of test item: 100, 1000 and 10000 mg/L
Test 2: nominal concentrations of test item: 1000, 1800, 3200, 5600 and 10000 mg/L
Nominal concentration of reference compound 3.5-Dichlorophenol: 1 and 20 mg/L - Details on test conditions:
- not reported
- Reference substance (positive control):
- yes
- Remarks:
- 3.5-Dichlorophenol was used as reference substance.
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 10 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Remarks on result:
- other: The test substance showed a respiration inhibition of 48% in test 1 and 31% in test 2 at the highest test itemconcentration of 10000 mg/L.
- Details on results:
- not reported
- Results with reference substance (positive control):
- The EC50 of 3.5-Dichlorophenol is in the range 5-30 mg/L.
- Reported statistics and error estimates:
- not reported
- Validity criteria fulfilled:
- yes
- Remarks:
- All validity criteria of the test method were met: - respiratory rates of the 2 controls differ less than 15% - EC50 of 3.5-Dichlorophenol is in the range 5-30 mg/L .
- Conclusions:
- Vulkanox BKF showed a respiration inhibition of 48% in test 1 and 31% in test 2 at the highest concentration tested, and hence:
EC50 > 10000 mg/L (based on nominal concentrations). - Executive summary:
A respiration inhibition test with activated sludge according to OECD Guideline 209 (1983) was conducted to assess the toxicity of BPH to bacteria. This test method is equal to ISO 8192 "Test for Inhibition of Oxygen Consumption of Activated Sludge".
The respiration rate of each mixture was determined after aeration periods of 3 hours. BPH showed a respiration inhibition of 48% in test 1 and 31% in test 2 at the highest concentration tested, and hence:
EC50 > 10000 mg/L (based on nominal concentrations).
Reference
In the following tables the respiration rate, the percentage of inhibition as well as the pH values at the different test concentrations were presented:
Test 1:
|
Test item concentration [mg/L] |
Respiration rate
[mg/(L*h)] |
Inhibition
% |
pH |
Test item |
100 |
28 |
0 |
8.1 |
1000 |
28 |
0 |
8.1 |
|
10000 |
14 |
48 |
8.1 |
|
Reference substance |
1 |
24 |
11 |
8.1 |
20 |
6 |
78 |
8.2 |
|
Control 1 |
|
27 |
- |
8.1 |
Control 2 |
|
27 |
- |
8.1 |
Test 2:
|
Test item concentration [mg/L] |
Respirationrate
[mg/(L*h)] |
Inhibition
% |
pH |
Test item |
1000 |
36 |
0 |
8.5 |
1800 |
36 |
0 |
8.5 |
|
3200 |
33 |
6 |
8.4 |
|
5600 |
30 |
14 |
8.4 |
|
10000 |
24 |
14 |
8.4 |
|
Reference substance |
1 |
33 |
6 |
8.3 |
20 |
8 |
77 |
8.5 |
|
Control 1 |
|
34 |
- |
8.2 |
Control 2 |
|
36 |
- |
8.4 |
Description of key information
The EC50 (3h) of DBMC for activated sludge was determined to be > 10 000 mg/L. No PNEC can be derived based on this result
Key value for chemical safety assessment
Additional information
A respiration inhibition test with activated sludge according to OECD Guideline 209 (1983) was conducted to assess the toxicity of DBMC to bacteria. This test method is equal to ISO 8192 "Test for Inhibition of Oxygen Consumption of Activated Sludge". The respiration rate of each mixture was determined after aeration periods of 3 hours. DBMC showed a respiration inhibition of 48% in test 1 and 31% in test 2 at the highest concentration tested (10 000 mg/L), and hence: EC50 > 10 000 mg/L (based on nominal concentrations).
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