Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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: 211-941-3 | CAS number: 717-74-8
- 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:
- Aug 5, 2015 to Sept 10, 2015
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Version / remarks:
- 2010
- Deviations:
- yes
- Remarks:
- one deviation noted; considered uncritical
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Version / remarks:
- 2008
- Deviations:
- yes
- Remarks:
- one deviation noted; considered uncritical
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: Batch No. 6F11027000
- Expiration date of the lot/batch: 17-Nov-2016
- Purity: 96% - Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- Due to the poor solubility of the test item, the test item was added directly into the test vessel using pipettes.
Tap water was used as the dilution water along with a nutrient solution. - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Name and location of sewage treatment plant where inoculum was collected: Collected from the activation basin of the ESN (Stadtentsorgung Neustadt) sewage treatment plant D-67435 NW-Lachen-Speyerdorf
- Method of cultivation: Field-collected
- Preparation of inoculum for exposure: sludge was filtrated, washed with tap water and re- suspended in tap water.
- Pretreatment: The activated sludge was aerated until usage in the test and fed daily with 50 mL synthetic sewage feed /L (the nutrient solution was thawed and the sludge was fed with 50 mL/L sludge)
- Initial biomass concentration: 2.52 g suspended solids/L - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 3 h
- Test temperature:
- 22.6 – 23.4°C
- pH:
- 7.6-8.0
- Nominal and measured concentrations:
- 1, 100, 1000 mg/L; Nominal concentrations.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 2000 mL Schott flasks (250-mL narrow-neck glass bottles with flat bottoms used as measuring flasks)
- Type: closed
- Material, size, headspace, fill volume: a large headspace
- No. of vessels per concentration (replicates): 5 replicates for 1000 mg/L test item concentration; 1 replicate for 100 mg/L test item concentration; 1 replicate for 10 mg/L test item concentration; 1 replicate for 1 mg/L test item concentration
- No. of vessels per control: 6 replicates
- No. of vessels per positive control: 4 replicates
- Sludge concentration: 1.26 g suspended solids/L - Reference substance (positive control):
- yes
- Remarks:
- 3,5-Dichlorophenole
- Key result
- Duration:
- 3 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other:
- Remarks:
- Calculated % Inhibition values are presented based on the O2 consumption measured (which is a measure for the viability of the bacteria). However it is not explicitly stated if this represents (total?) respiration.
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other:
- Remarks:
- Calculated % Inhibition values are presented based on the O2 consumption measured (which is a measure for the viability of the bacteria). However it is not explicitly stated if this represents (total?) respiration.
- Duration:
- 3 h
- Dose descriptor:
- EC10
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other:
- Remarks:
- Calculated % Inhibition values are presented based on the O2 consumption measured (which is a measure for the viability of the bacteria). However it is not explicitly stated if this represents (total?) respiration.
- Results with reference substance (positive control):
- Four concentrations were tested; an EC50 of 8.9 mg/L (95% confidence interval: 7.3 – 11 mg/L) was determined, which lies within the range of 2 – 25 mg/L.
- Reported statistics and error estimates:
- For the treatments with the test item concentration 1000 mg/L, it was tested whether the differences between treatment and control were significant. Equality of variance was tested (F-value), followed by a t-test.
The difference between treatment 1000 mg/L and the control was considered as not significant as the calculated t-value lay below the significance level. Therefore, the concentration 1000 mg/L is stated as NOEC. - Validity criteria fulfilled:
- yes
- Conclusions:
- The test item was tested using 4 concentrations ranging from 1000 to 1 mg/L nominal con-centration. As the test item is volatile, the experiment was performed in a closed system without aeration. Under the test conditions, the 3-hr EC10 and 3-hr EC50 were determined to be > 1000 mg/L (nominal).
- Executive summary:
The effect of 1,3,5-triisopropylbenzene was tested under static conditions in a 3-hour activated sludge respiration inhibition study with 4 concentrations according to OECD TG 209. Based on nominal concentrations, the 3-h NOEC was determined to be 1000 mg/L.
Reference
Summary of validation criteria:
- The coefficient of variation of oxygen uptake rate in control replicates (8.0%) did not exceed 30% at the end of the test
- The blank controls oxygen uptake rate (41.50 mg oxygen per gram sludge in 1 hour) was less than 20 mg oxygen per gram of activated sludge (dry weight of suspended solids) in 1 hour
The following deviations from the study plan were reported:
- The temperature in the Test was in a range of 22.6 – 23.4°C instead of 20 ± 2°C.This deviation was stated as uncritical, as normal respiration activity of the control could be observed.
- The test item was stored from the date of receipt to last usage for the study at 20 ± 5°C except of 10 days below 15°C and short-term for 25.8°C. This is considered as uncritical concerning the outcome of the study.
- The concentration in the lowest concentration was 1.7 mg/L instead of 1 mg/L because direct addition of 1 mg/L (corresponding to 0.56 µL / 500 mL Test solution) is not possible.
Description of key information
The effect of 1,3,5-triisopropylbenzene was tested under static conditions in a 3-hour activated sludge respiration inhibition study with 4 concentrations according to OECD TG 209. Based on nominal concentrations, the 3-h NOEC was determined to be 1000 mg/L.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 mg/L
- EC10 or NOEC 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.
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.