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EC number: 947-340-4 | CAS number: -
- 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:
- 2011-12-07 - 2012-01-30
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The GLP study was conducted according to an internationally accepted guideline. All study parameters are given in detail.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Details on sampling:
- In the control vessels 16 mL nutrient solution were mixed with 234 mL water. The positive control and the treatments were prepared by putting the appropriate amount of positive control solution respectively test item into the test vessel, adding 16 mL nutrient solution and water to give 250 mL. Then, 250 mL inoculum was added in five minute intervals and the mixture was aerated.
After three hours, the content of the first vessel was poured in a 250 mL narrow-neck bottle and the respiration rate was determined by measurement of the 02-concentration over a period of five minutes1. The following vessels were measured likewise in five minute intervals. - Vehicle:
- no
- Details on test solutions:
- Chemicals and Nutrient Solution
All chemicals used in the test were "analytical grade" or "for use in microbiology".
Composition of nutrient solution (synthetic sewage):
Peptone 16.0 g
Meat Extract 11.0 g
Urea 3.0 g
NaCI 0.7 g
CaCI2*2H20 0.4 g
MgS04*7H20 0.2 g
K2HP04 2.8 g
Deionised water ad 1000 mL
The measured pH of the solution was 7.1. Therefore no pH adjustment to pH 7.5 ± 0.5 was necessary.
The nutrient solution was freshly prepared; the inoculum was taken from its source, washed, aerated and the dry matter was determined. The stock solutions of the test item and the positive control were prepared.
Concentrations of test and positive control were calculated using the concentration of the respective stock solution and the dilution factor.
The test item was added to the test vessels directly. - Test organisms (species):
- activated sludge, domestic
- Details on inoculum:
- The sludge was taken from the activation basin of the ESN (Stadtentsorgung Neustadt) sewage treatment plant D-67435 NW-Lachen-Speyerdorf and aerated during transport.
Upon arrival in the test facility, the sludge was filtrated, washed with tap water and re-suspended in tap water. The activated sludge was aerated until usage in the test and fed daily with 50 ml /L synthetic sewage feed. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Hardness:
- 1.08 mmol/l
- Test temperature:
- 18.1-18.8 "C
- pH:
- 7.9 - 8.1
- Nominal and measured concentrations:
- Nominal:
1008, 1068, 1036, 1086, 1040, 101.4, 11.2, 1 mg/l - Reference substance (positive control):
- yes
- Remarks:
- 3,5-Dichlorophenol
- Key result
- Duration:
- 3 h
- Dose descriptor:
- other: EC20
- Remarks:
- EC20
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 3 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Details on results:
- see below
- Results with reference substance (positive control):
- see below
- Validity criteria fulfilled:
- yes
- Conclusions:
- The following results for the test item Ukanol FR 70 were determined:
3h NOEC = 1000 mg/L
3h EC20 > 1000 mg/L
3h EC50 > 1000 mg/L - Executive summary:
The toxicity of Ukanol FR 70 towards microorganism was assessed according to OECD test method 209. One experiment was performed. As the EC50 was found as > 1000 mg/L and the highest test concentration of 1000 mg/l showed no significant inhibition, no further testing was done. All validity criteria were met. For the estimation of the EC50 of the positive control 3,5-dichlorophenole, the fit showed good statistical correspondence of the data with the dose-response-equation. The positive control gave an EC50 of 8.3 mg/L which is within the recommended range of 2 - 25 mg/L. The coefficient of variation of oxygen uptake rate in control replicates was below 30% at the end of the test. In the all treatments (range 1000 - 1 mg/L), no inhibition could be observed. The O2-consumption in all replicates of treatment 1000 mg/L was higher than the mean of the controls. Therefore 1000 mg/L can be stated as NOEC without an additional experiment for statistical determination.
Reference
Vessel |
Content |
Concentration |
02consump |
02consump |
Inhibition |
pH |
No. |
|
in mg/L |
tion in |
tion in |
in% |
|
|
|
|
mg/(L*min.) |
mg/(L*h) |
|
|
1 |
Control |
0 |
0.4495 |
26.970 |
|
8.0 |
2 |
Control |
0 |
0.4290 |
25.738 |
— |
8.0 |
3 |
Positive Control |
5 |
0.3011 |
18.063 |
34.5 |
8.1 |
4 |
Positive Control |
10 |
0.1958 |
11.748 |
57.4 |
8.1 |
5 |
Positive Control |
20 |
0.1201 |
7.205 |
73.9 |
8.1 |
6 |
Positive Control |
40 |
0.0683 |
4.097 |
85.1 |
8.2 |
7 |
Control |
0 |
0.4705 |
28.230 |
— |
8.0 |
8 |
Control |
0 |
0.4625 |
27.748 |
|
8.0 |
9 |
Test Item |
1008 |
0.4706 |
28.235 |
-2.4 |
8.0 |
10 |
Test Item |
1068 |
0.4832 |
28.991 |
-5.1 |
7.9 |
11 |
Test Item |
1036 |
0.4849 |
29.095 |
-5.5 |
7.9 |
12 |
Test Item |
1086 |
0.4732 |
28.394 |
-2.9 |
7.9 |
13 |
Test Item |
1040 |
0.4872 |
29.231 |
-6.0 |
7.9 |
14 |
Test Item |
101.4 |
0.4800 |
28.798 |
-4.4 |
7.9 |
15 |
Test Item |
11.2 |
0.4662 |
27.973 |
-1.4 |
7.9 |
16 |
Test Item |
1.0 |
0.4765 |
28.590 |
-3.6 |
8.0 |
17 |
Control |
0 |
0.4738 |
28.431 |
— |
8.0 |
18 |
Control |
0 |
0.4733 |
28.400 |
|
8.0 |
Description of key information
The following results for the test item Ukanol FR 70 were determined:
3h NOEC = 1000 mg/L
3h EC20 > 1000 mg/L
3h EC50 > 1000 mg/L
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 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.
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