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EC number: 202-114-8 | CAS number: 91-99-6
- 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:
- 22 November 1999 - 26 November 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- 1992
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: control and 100 mg/L
- Sampling method: at t=0, 24, 48, 72 and 96 h - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: the test item was directly added to the test medium at a concentration of 100 mg/L. The solution was stirred on a magnetic stirrer for 2 hours before the start of the test.
- Controls: yes, medium without additives was used as a conrol. - Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: zebrafish
- Strain: Hamilton Buchanan
- Source: Bio International B.V. (The Netherlands)
- Age at study initiation (mean and range, SD): approx. 6 months old
- Length at delivery: 2.5 - 3.5 cm
- Delivery date: 1999-09-09
- Mortality: <2% mortality was observed during the period between delivery of the fish and the experimental start date.
- Acclimation conditions: synthetic freshwater according to ISO
FEEDING DURING TEST : not indicated - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- 244.52 CaCO3/L (13.7 deutscher Härtegrad)
- Test temperature:
- Control and 100 mg/L: 21.1 - 21.9 °C throughout the test
- pH:
- Control and 100 mg/L: 7.6-7.9 throughout the test
- Dissolved oxygen:
- Control: 8.5 - 8.9 mg O2/L throughout the test
100 mg/L: 8.6 - 8.9 mg O2/L throughout the test - Nominal and measured concentrations:
- Nominal concentration: 100 mg/L
Measured concentrations: 71, 68, 68, 68 and 68 mg/L at t=0, 24, 48, 72 and 96 h, respectively. - Details on test conditions:
- TEST SYSTEM
- Test vessel: aquaria with a size of 300 x 135 x 200 mm, fill volume: 5 L
- Aeration: yes
- No. of organisms: 10 for the test solution and 10 for the control
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: synthetic freshwater according to ISO
OTHER TEST CONDITIONS
- Photoperiod: 16 hours light/8 hours dark
EFFECT PARAMETERS MEASURED: mortality at t=2, 24, 48, 72 and 96 h
RANGE-FINDING STUDY: no range-finding study was conducted - Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 68.6 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- other: Based on TOC measurements
- Basis for effect:
- mortality (fish)
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 102 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Remarks:
- Calculated test item concentration from TOC measurements
- Basis for effect:
- mortality (fish)
- Details on results:
- - No mortality was observed in control and at the tested concentration of 100 mg/L
- No behavioural abnormalities were observed throughout the test for both control and test item concentration 100 mg/L
- The report indicated a 96h-LC0 of > 102.9 mg/L. However, based on the measured concentrations, an arithmetic mean exposure concentration of 68.6 mg/L was calculated by the applicant.
- Length at study end: 2.7 - 3.5 cm (control and 100 mg/L)
- Weight at study end, average of 10 fish: 0.364 g (control) and 0.325 g (100 mg/L) - Validity criteria fulfilled:
- yes
- Remarks:
- See 'Overall Remarks'
- Conclusions:
- The 96h-LC50 of N,N-Bis-(hydroxyethyl)-m-toluidin was determined in a limit test according to EU method C.1 to exceed the tested concentration (i.e. >68.6 mg/L, mean measured exposure concentration based on TOC measurement).
- Executive summary:
An acute fish toxicity test was performed according to EU method C.1. A concentration of 100 mg/L of the test item was directly applied to the test medium, the test solution was stirred for 2 hours on a magnetic stirrer and this solution was used as the test solution. Ten zebrafish were exposed to the limit concentration and a control for 96 hours. Observations for mortality were made at t=2, 24, 48, 72 and 96 h. Samples taken from the test solution and the control at t=0, 24, 48, 72 and 96 h were analysed by TOC analysis. Measured concentrations were 71 -68 mg/L. During the exposure period, no mortality occurred and no abnormalities were observed. Therefore, the LC50 was determined to exceed the limit concentration tested, i.e. >68.6 mg/L based on the mean measured exposure TOC concentration, corresponding to >102 mg/L test item.
Reference
Description of key information
In a limit study according to EU method C.1, the 96h-LC50 for freshwater fish was determined to be >102 mg/L based on mean measured concentration.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 102 mg/L
Additional information
An acute fish toxicity test was performed according to EU method C.1. A concentration of 100 mg/L of the test item was directly applied to the test medium, the test solution was stirred for 2 hours on a magnetic stirrer and this solution was used as the test solution. Ten zebrafish were exposed to the limit concentration and a control for 96 hours. Observations for mortality were made at t=2, 24, 48, 72 and 96 h. Samples taken from the test solution and the control at t=0, 24, 48, 72 and 96 h were analysed by TOC analysis. Measured concentrations were 71 -68 mg/L. During the exposure period, no mortality occurred and no abnormalities were observed. Therefore, the LC50 was determined to exceed the limit concentration tested, i.e. >68.6 mg/L based on the mean measured exposure TOC concentration, corresponding to >102 mg/L test item.
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