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EC number: 223-861-6 | CAS number: 4098-71-9
- 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

Short-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1999-09-27 to 1999-10-01
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions: test substance not stable under test conditions (rapid hydrolysis)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- Cited as Directive 92/69/EEC, C.1
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - daily sampling
- Vehicle:
- no
- Details on test solutions:
- STOCK AND TEST SOLUTION AND THEIR PREPARATION
- Dispersion: A 1.3 fold amount (100 mg/l) of the maximum water solubility of the test substance in the preliminary test (70 mg/l) was weighed into water, treated for 60 seconds at 8000 rpm with an ultra-turrax and afterwards stirred on a magnetic stirred for 24 hours. The resulting emulsion
was filtered using a folded filter of pore size 7-12 um. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISMS
- Strain: Danio rerio (formerly Brachydanio rerio) HAMILTON BUCHANAN
- Supplier: Bio International B.V. (The Netherlands)
- Age/size/weight/loading: age 6 months 23 days, total weight of 10 fish at test end 3.62 g (10 control fish: 4.83 g), length 2.5 - 3.5 cm
- Keeping water: synthetic fresh water in accordance with ISO
- Pretreatment: no medical pretreatment - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- 14.0 degree German hardness
- Test temperature:
- 21.4-21.5 (control: 21.4-21.7) degree C
- pH:
- pH: 7.6-8.0 (control: 7.7-8.1)
- Dissolved oxygen:
- 8.2-8.5 = 95.1-98.7 % saturation
(control: 8.3-8.4 mg/l = 96.3-97.4 % saturation) - Nominal and measured concentrations:
- 70 mg/L (nominal)
- Details on test conditions:
- DILUTION WATER
- Synthetic fresh water in accordance with ISO
CONTROLS
- Synthetic fresh water in accordance with ISO, Hardness: 14.0 degree German hardness
TEST SYSTEM
- Concentration: 70 mg/l
- Exposure vessel type: 300 x 135 x 200 mm with 5 l test medium, ventilated
- Number of replicates, fish per replicate: 1 replicate with 10 fish each for exposed and control
- Photoperiod: 16 hours light / 8 hours dark
TEST PARAMETER
- mortality and visible effects (swimming behavior)
- observations at 2, 24, 48, 72, and 96 hours - Reference substance (positive control):
- not specified
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 72 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: TOC measurement
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 72 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- other: TOC measurement
- Basis for effect:
- mortality (fish)
- Details on results:
- No mortality was observed in control and treated fish. The swimming behavour was found to be normal.
- Sublethal observations / clinical signs:
RESULTS:
- Nominal/measured concentrations:
nominal: 70 mg/l; arithmetic mean analytical 72.3 mg/l
analytical TOC at
0 h: 48 mg/l; 24 h: 49 mg/l; 48 h: 48 mg/l;
72 h: 47 mg/l; 96 h: 49 mg/l
control: always < 2 mg/l
The TOC has to be multiplied with 1.5 to correspond with the amount of test substance.- Validity criteria fulfilled:
- yes
- Conclusions:
- The LC50 (96h) was found to be > 72 mg/L (arithmetic mean of analytical measured values) since no mortalities and abnormal swimming behaviour were
observed during the test. Furthermore, the mean measured concentration of the substance during the test is higher than its maximum determined water solubility of 15 mg/l (23°C). - Executive summary:
A static acute 96-hour fish toxicity limit test according to Directive 92/69/EEC was performed with Danio rerio (Bayer AG 2000). No mortalities and no abnormal swimming behaviour were observed (96h-LC50 >72 mg/L) at the tested concentration (70 mg/L nominal).
Due to fast hydrolysis it is assumed that the observed effect is rather attributed to the hydrolysis product than to the parent substance.
The study was assessed as "reliable with restrictions".
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1996-10-21 to 1996-10-25
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study with acceptable restrictions: Test substance not stable under test conditions (rapid hydrolysis)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- Cited as Directive 92/69/EEC, C.1
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - analysis of stock solution twice at 0 h and once after 48 h
- Vehicle:
- no
- Details on test solutions:
- STOCK AND TEST SOLUTION AND THEIR PREPARATION
- 1 g test substance was stirred for approx. 18 hours in water and filtered. Test solutions were prepared daily.
STABILITY OF THE TEST CHEMICAL SOLUTIONS
- Hydrolysis was expected but not quantified. TOC analysis after 24 hours indicated that losses were insignificant (less than 20 % compared to nominal concentrations). - Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- TEST ORGANISMS
- Supplier: Bio International B.V., Someren (NL)
- Age/size/weight/loading: length 2-3 cm, weight approx. 0.36 g
- kept in dechlorinated tap water in 300 L container
- Feeding: approx. 1 % of body weight daily (TRUOVIT)
- Pretreatment: 14 days quarantine
- Feeding during test: no - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- - approx. 11 °dH (German hardness)
- Test temperature:
- 18.1-21.5 °C,
mean: 20 °C - pH:
- - 7.7-8.3
- Dissolved oxygen:
- - 88-100 % saturation
- Nominal and measured concentrations:
- - 28; 46; 81; 139; 231 mg/l (nominal)
- 28; 46; 81; 139; 208 mg/l (used for evaluation, highest concentration is the arithmetic mean of measured values)
The maximum concentration of 231 mg/l could not be achieved every day. Thus the mean of the highest test concentrations was used for
evaluation. - Details on test conditions:
- DILUTION WATER
- Source: drinking water (Gelsenwasser AG)
- Aeration: continuously during test
TEST SYSTEM
- Exposure vessel type: approx. 20 l aquaria with 10 l test solution
- Number of replicates, fish per replicate: one replicate with 10 fish
TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 / 8 hours - Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- >= 208 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: TOC measurement
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 208 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: TOC measurement
- Basis for effect:
- mortality (fish)
- Details on results:
- No mortality was observed in the control and the treated animals
- Sublethal observations / clinical signs:
RESULTS:
- Nominal/measured concentrations:
- nominal: 28; 46; 81; 139; 231 mg/l
- 0 h (first analysis): 25; 45; 81; 134; 231 mg/l
- 0 h (second analysis): 27; 44; 78; 138; 178 mg/l
- 24 h (single analysis): 25; 48; 84; 147; 251 mg/l
- Effect data (mortality): no deaths in exposed or control animals- Validity criteria fulfilled:
- not specified
- Conclusions:
- No effects were observed at the tested concentrations. Hence the LC50 (96 hours) was determined to be >208 mg/L indicating that the test substance does not present a significant hazard to fish.
- Executive summary:
In a semi-static acute fish toxicity test according to Directive 92/69/EEC, Hüls AG (1996) observed no mortalities in Cyprinus carpio within 96 hours of exposure to concentrations up to the maximum possible concentration of 208 mg/l (arithmetic mean of analyses for four days). Hence the LC50 (96 hours) was determined as >208 mg/L.
Due to fast hydrolysis it is assumed that the observed effect is rather attributed to the hydrolysis product than to the parent substance.
The study was assessed as "reliable with restrictions".
Referenceopen allclose all
Description of key information
A static acute 96-hour fish toxicity limit test according to Directive 92/69/EEC was performed with Danio rerio (Bayer AG, 2000). No mortalities or abnormal swimming were observed. The analytical test concentration, which was determined daily by DOC measurements, was 72.3 mg/l. In a semi-static acute fish toxicity test according to Directive 92/69/EEC, Hüls AG (1996) no mortalities in Cyprinus carpio within 96 hours of exposure to concentrations up to the maximum possible concentration of 208 mg/l were observed.
Key value for chemical safety assessment
Additional information
The LC50 values for Danio rerio and Cyprinus carpio were determined as >72 mg/L and >208 mg/L, respectively. In view of the low solubility in water (see chapter 4.9) and the liability towards hydrolysis (see chapter 5.1.2) of 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate, exposure to well-defined aquatic concentrations is difficult to achieve. Due to fast hydrolysis, the observed effect is expected to be the effect of the hydrolysis product. In the aquatic environment, only the chemically less reactive hydrolysis product is expected to be relevant. The methods used for the determination of the test substance concentration (DOC or TOC) do not differentiate between parent substance and hydrolysis product. Hence the analytical results should be treated with caution.
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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