Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 218-485-4 | CAS number: 2162-73-4
- 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
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP guideline study with acceptable restrictions.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Version / remarks:
- (ISO 8192-1986)
- Deviations:
- no
- Remarks:
- not reported
- GLP compliance:
- no
- Remarks:
- No public authority statement included.
- Analytical monitoring:
- not specified
- Details on sampling:
- No details are reported.
- Vehicle:
- no
- Details on test solutions:
- No details are reported.
- Test organisms (species):
- activated sludge
- Details on inoculum:
- No further details are reported.
Prepared according to ISO 8192-1986: Chapter 4.2 - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 3 h
- Remarks on exposure duration:
- no remarks
- Post exposure observation period:
- No details are reported.
- Hardness:
- No details are reported.
- Test temperature:
- 20.5 °C- 21.1 °C
(Control: 20.5 - 20.7) - pH:
- 7.4 - 7.8
(Control: 7.9) - Dissolved oxygen:
- 5.4 - 8.7 mg (start)
4.6 - 8.7 mg (end) - Salinity:
- No details are reported.
- Nominal and measured concentrations:
- 100, 1000 and 10000 mg/L
- Details on test conditions:
- No further details are reported.
- Reference substance (positive control):
- yes
- Remarks:
- 3,5 Dichlorphenol
- 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: remark: water-insoluble
- Details on results:
- - 0.00 % inhibiton at quantities of 25.00 (= 100 mg/L) and 250.00 mg (=1000 mg/L)
- 11.1 % inhibiton at a quantity of 2500.00 mg (= 10000 mg/L) - Results with reference substance (positive control):
- - Results with reference substance valid? yes
- Results: 0.00 % inhibition at a quantity of 0.25 mg
66.7 % inhibition at a quantity of 5.00 mg - Reported statistics and error estimates:
- No details are reported.
- Validity criteria fulfilled:
- yes
- Remarks:
- Experiment in accordance with above mentioned study method
- Conclusions:
- The study is regarded as a valid guideline study without GLP compliance. According to the reported results no evidence can be found that the test substance has a toxic effect to microorganisms present in activated sludge.
- Executive summary:
The acute toxicity to microorganisms of the substance 2,4,6 -triisopropyl-m-phenylene diisocyanate was investigated in accordance with OECD Guideline 209 without GLP compliance (Kanne, R., 1989). Activated sludge was used in the static freshwater experiment with an exposure time to the test substance of 3 hours. The culture medium was prepared according to ISO 8192 -1986, Chapter 4.2. The temperature range was 20.5 - 21.1 °C (Control: 20.5 - 20.7 °C) and the pH was adjusted in the range of 7.4 - 7.8 (Control: 7.9). The dissolved oxygen was 5.4 - 8.7 mg at the beginning and 4.6 - 8.7 mg at the end of the experiment. The test substance was tested in the concentrations of 100, 1000 and 10000 mg/L. 3,5 -Dichlorphenol was used as reference substance and showed 66.7 % inhibition at a used quantity of 5.00 mg. Regarding the test substance an inhibition of 11.1 % was reported at a quantity of 2500 mg, which reveals a concentration of 10000 mg/L. Additionally, an EC50 (3h) value of >= 10000 mg/L is given as result, but with the remark of water insolubility.
Reference
Table 4: Test results
|
Quantity (mL/mg) |
O2-Start-Value (mg) |
O2-End-Value (mg) |
Time (min) |
Temp (°C) |
pH |
Inhibition (%) |
|
1 |
Sludge |
25.000 |
|
|
|
|
|
|
2 |
Test substance |
25.000 |
5.80 |
5.20 |
2.0 |
21.1 |
7.8 |
0.00 |
3 |
Test substance |
250.000 |
6.30 |
6.00 |
1.0 |
21.1 |
7.8 |
0.00 |
4 |
Test substance |
2500.000 |
5.40 |
4.60 |
3.0 |
21.1 |
7.7 |
11.1 |
5 |
Reference substance |
0.250 |
6.00 |
5.10 |
3.0 |
20.5 |
7.9 |
0.00 |
6 |
Reference substance |
5.000 |
8.30 |
8.20 |
1.0 |
20.7 |
7.9 |
66.7 |
7 |
Control (start) |
0.000 |
5.80 |
4.90 |
3.0 |
20.5 |
7.8 |
0.00 |
8 |
Control (end) |
0.000 |
5.60 |
5.00 |
2.0 |
21.0 |
7.8 |
0.00 |
9 |
Autoxidation |
2.500.000 |
8.70 |
8.70 |
10.0 |
21.0 |
7.4 |
0.00 |
EC 50 => 10000 mg/L |
Description of key information
Toxicity to microorganisms: EC50 (3h) >= 10000 mg/L for activated sludge (non-GLP, OECD TG 209, static)
Key value for chemical safety assessment
- EC50 for microorganisms:
- 10 000 mg/L
Additional information
The acute toxicity to microorganisms of the substance 2,4,6-triisopropyl-m-phenylene diisocyanate was investigated in accordance with OECD Guideline 209 without GLP compliance (Kanne, 1989). Activated sludge was used in the static freshwater experiment with an exposure time to the test substance of 3 hours. The culture medium was prepared according to ISO 8192 -1986, Chapter 4.2. The temperature range was 20.5 - 21.1 °C (Control: 20.5 - 20.7 °C) and the pH was adjusted in the range of 7.4 - 7.8 (Control: 7.9). The dissolved oxygen was 5.4 - 8.7 mg at the beginning and 4.6 - 8.7 mg at the end of the experiment. The test substance was tested in the concentrations of 100, 1000 and 10000 mg/L. 3,5 -Dichlorphenol was used as reference substance and showed 66.7 % inhibition at a quantity of 5.00 mg. Regarding the test substance an inhibition of 11.1 % was reported at a quantity of 2500 mg, which reveals a concentration of 10000 mg/L. Additionally, an EC50 (3h) value of >= 10000 mg/L is reported as result, but with the remark of water insolubility.
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.
