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EC number: 216-835-0 | CAS number: 1678-91-7
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1996-12-25 - 1997-03-04
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I))
- Deviations:
- not specified
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Purity 99.5%
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Details on inoculum:
- Sampling method
(1) Urban wastewater: Returned sludge from sewage plants
(2) River, lakes, marshes and sea: The surface soil in the area of where the surface water and atmosphere converge
Mixing the old and new sludge:
The filtrate of the sludge sampled from the locations specified above (500mLeach) and the filtrate of old, previously tested activated sludge (5L) were mixed to prepare 10L, pH was adjusted to 7.0±1.0, and the mixture was aerated in the incubation tank.
Aeration:
External air was processed through a prefilter and used for aeration.
Incubation:
After pausing aeration of the incubation tank for approximately 30 minutes, approximately 1/3 volume of the total amount of supernatant was discarded. An equal amount of dechlorinated water was added and the aeration was resumed, and then synthetic sewage water*3was added to give a concentration of 0.1%inthe replaced supernatant. This operation was repeated once daily for incubation,and the resulting matter was used as activated sludge. The incubation was performed at temperature of 25°C±2°C.
Synthetic sewage water:
Glucose, peptone, and potassium dihydrogen phosphate were dissolved in dechlorinated water to give 5(W/V)%,and the pH was adjusted with sodium hydroxide to 7.0±1.0.
Control and use:
During incubation, appearance of the supernatant and formation of activated sludge were observed, and activated sludge was measured and recorded in terms of sedimentation, pH and temperature, and dissolved oxygen concentration. The biota of the activated sludge was observed using light microscopy as needed to ensure that no abnormalities were identified before use for the test.
Inspection of the activity and date of starting the use of activated sludge :
Examination of activity in activated sludge
The activity was examined before starting to use the activated sludge by using the reference standard material. In addition, the association with the old activated sludge was monitored. - Duration of test (contact time):
- 28 d
- Initial conc.:
- 100 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- Test solution incubation apparatus Closed system oxygen consumption measurement apparatus (coulometer, Okura Electric)
(Data processor, Asahi Techneion)
Study container 300 mL incubation bottle (modified type for volatile substance)
Carbon dioxide absorbent Soda lime, No. 1
(Wako Pure Chemical Industries, for carbon dioxide absorption)
Stirring method rotational stirring using a magnetic stirrer
Environmental condition Test solution incubation temperature 25°C ± 1°C
Test solution incubation period For 28 days - Reference substance:
- aniline
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 28 d
- Key result
- Parameter:
- % degradation (test mat. analysis)
- Value:
- 0
- Sampling time:
- 28 d
- Results with reference substance:
- The degradation of aniline on days7and 14calculated from the BOD were 72%and 99%, respectively, demonstrating that the operating conditions used in this study were effective.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The test result showed 0 % degradation by BOD and it was confirmed by the direct analysis with gas chromatography that more than 94 % of ethylcyclohexane remained after the cultivation period. Therefore, ethylcyclohexane is not readily biodegradable.
- Executive summary:
The test result showed 0 % degradation by BOD and it was confirmed by the direct analysis with gas chromatography that more than 94 % of ethylcyclohexane remained after the cultivation period. Therefore, ethylcyclohexane is not readily biodegradable.
Reference
Description of key information
Ethylcyclohexane was tested for ready biodegradation in a Modified MITI Test according to OECD Guideline 301 C.
The test result showed 0 % degradation by BOD and it was confirmed by the direct analysis with gas chromatography that more than 94 % of ethylcyclohexane remained after the cultivation period. Therefore, ethylcyclohexane is not readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
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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