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EC number: 309-304-0 | CAS number: 100208-97-7
- 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
Toxicity to aquatic plants other than algae
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic plants other than algae
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 22 January - 03 July 2018
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 221 (Lemna sp. Growth Inhibition Test)
- Version / remarks:
- 23rd March, 2006
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Commission Regulation (EC) No 761/2009, Annex VI, C.26: „Lemna sp. Growth Inhibition Test“. Dated 24 August 2009
- Version / remarks:
- 24 August 2009
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures, section 3.1.2 Media preparation methods, Direct addition. OECD Series on Testing and Assessment No. 23, Paris September 2000
- Version / remarks:
- September 2000
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- Date of production:22 February 2016
Expiry date: 22 February 2021 - Analytical monitoring:
- yes
- Details on sampling:
- Based on the results of the preliminary experiment, the nominal concentrations of 6.25, 12.5, 25.0, 50.0 and 100 mg test item/L were investigated in the main study. The measured concentrations deviated more than 20 % from the nominal at the start and at the end of the study, therefore the geometric mean of the measured concentrations were calculated to determine exposure concentration. The corresponding calculated concentrations were 0.10, 0.30, 0.55, 0.91 and 1.69 mg/L, equivalent to the nominal 6.25, 12.5, 25.0, 50.0 and 100 mg test item/L, respectively (based on total product). Biological results and endpoints are based on the measured and calculated concentrations.
- Vehicle:
- no
- Details on test solutions:
- As the test item is poorly soluble in deionized water as well in the test medium, preparation of test solutions was performed using the WAF method (according to OECD Series on Testing and Assessment No. 23). The appropriate test item amounts were suspended in the appropriate amounts of the dilution water (20X AAP Medium; see 5.4) in order to give the loading rates of 6.25, 12.5, 25.0, 50.0 and 100 mg test item/L. The test suspensions were handled in ultrasonic bath for 10 minutes thereafter stirred rigorously for a period of 24 hours to achieve equilibrated test concentrations. These test suspensions were then filtrated through a membrane filter* (0.45 µm) to separate the possible non-dissolved test material. The test solutions were freshly prepared in the testing laboratory just before introduction of the test organisms at the start of the test.
- Test organisms (species):
- Lemna gibba
- Details on test organisms:
- TEST ORGANISM
- Common name (Strain): Lemna gibba (G3)
- Source: Friedrich Schiller Universität, Institut für Allgemeine Botanik und Pflanzenphysiologie,Jena, Germany
- Preculture: 7 days before testing, sufficient colonies were transferred from the stock culture aseptically into fresh sterile medium and cultured under the conditions of the test prior to beginning the test.
- Initial frond number: The initial frond number in the test cultures was 11. The number of colonies and fronds was identical in each test vessel.
- Replicates and controls: The test included three replicates at each test concentration and six replicates for the control group - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 7 d
- Remarks on exposure duration:
- The study was performed over an exposure period of 7 days in 20X AAP Medium.
- Post exposure observation period:
- none
- Hardness:
- not measured
- Test temperature:
- The cultures were maintained at a temperature in the range of 24 +/- 2 ºC (22.6 – 25.8°C in the climate chamber and 23.0 – 23.9 °C in the test vessels), which was checked at the beginning of the study and every 24 hours (in a surrogate flask filled with water in the climate chamber). In addition, the temperature was continuously measured (with a min/max thermometer) within the climate chamber during the experimental period.
- pH:
- The pH was checked at the start and at the end of the test in the test concentrations and in the control. The pH of the control medium did not increase by more than 1.5 units. The pH values ranged between 7.86 - 8.88 during the test.
- Dissolved oxygen:
- not measured
- Salinity:
- not applicable
- Conductivity:
- not applicable
- Nominal and measured concentrations:
- The corresponding measured concentrations were 0.10, 0.30, 0.55, 0.91 and 1.69 mg/L, equivalent to the nominal 6.25, 12.5, 25.0, 50.0 and 100 mg test item/L, respectively (based on total product).
- Details on test conditions:
- The test containers were kept during the test in a climate chamber with controlled environmental conditions.
Test type: Static test. Based on the results obtained during analytical method validation (Study number: 805-100-2578) the test item is stable for the duration of 7 days in 20X AAP Medium. Therefore no renewal of the test and control solutions was necessary during the test.
Temperature: The cultures were maintained at a temperature in the range of 24 +/- 2 ºC (22.6 – 25.8°C in the climate chamber and 23.0 – 23.9 °C in the test vessels), which was checked at the beginning of the study and every 24 hours (in a surrogate flask filled with water in the climate chamber). In addition, the temperature was continuously measured (with a min/max thermometer) within the climate chamber during the experimental period.
pH: The pH was checked at the start and at the end of the test in the test concentrations and in the control. The pH of the control medium did not increase by more than 1.5 units. The pH values ranged between 7.86 - 8.88 during the test.
Light intensity: The test vessels were placed randomly on a tray, illuminated continuously at a light intensity between 6500-10000 lux (measured 7945 - 8025 lux, SD: 25 lux) using fluorescent light tubes (with a spectral range of 400-700 nm). The light intensity was checked and recorded at the start of the test at the position occupied by test containers. The differences in light intensity between the measurement points (i.e. position of fronds) did not exceed +/- 15 % and therefore provided equal conditions for each test culture.
Test units: All-glass beakers (total capacity of 400 mL) were used and were covered by glass petri dishes. The volume of the test liquid in the vessels was 160 mL. Each test unit was uniquely identified with study code, test item concentration (and control) and replicate. - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol is tested at least twice a year.
- Duration:
- 7 d
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 7 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 7 d
- Dose descriptor:
- EC10
- Effect conc.:
- > 1.69 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: EC10 is higher than the nominal concentration of 100 mg/L of the test item in the test medium, which corresponds to the mean measured concentration of 1.69 mg/L
- Key result
- Duration:
- 7 d
- Dose descriptor:
- EC50
- Effect conc.:
- > 1.69 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: the EC50 is higher than the nominal concentration of 100 mg/L of the test item in the test medium, which corresponds to the mean measured concentration of 1.69 mg/L
- Duration:
- 7 d
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.69 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: the test item had no toxic effect at aquatic saturation on Lemna gibba
- Duration:
- 7 d
- Dose descriptor:
- LOEC
- Effect conc.:
- > 1.69 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: the overall LOEC is higher than the nominal concentration of 100 mg/L of the test item in the test medium, which corresponds to the mean measured concentration of 1.69 mg/L
- Details on results:
- Biological Results
All biological results are based on the calculated mean concentrations (based on total product).
Growth Rate
The average specific growth rate was not statistically significantly different from the control group at any observed test item concentration based on frond number and dry weight (Dunnett t-test, one-sided, α=0.05).
The 168-h NOEC was determined to be 1.69 mg/L, while the 168-h LOEC was determined to be greater than 1.69 mg/L (solubility level of the highest loading rate of 100 mg/L in the test medium).
Yield
The yield was not statistically significantly different from the control group at any observed test item concentration based on frond number and dry weight (Dunnett t-test, one-sided, α=0.05).
The 168-h NOEC was determined to be 1.69 mg/L, while the 168-h LOEC was determined to be greater than 1.69 mg/L (solubility level of the highest loading rate of 100 mg/L in the test medium). - Results with reference substance (positive control):
- For the evaluation of the quality of the Lemna gibba cultures and the experimental conditions, 3,5-dichlorophenol is tested at least twice a year to demonstrate satisfactory test conditions.
The date of the last study (Study number: 392-221-3267) with reference item 3,5-dichlorophenol was: 08 – 15 September 2017.
Endpoints of this study were: EyfnC50 (7 day, yield based on frond numbers): 3.980 mg/L, ErfnC50 (7 day, growth rate based on frond numbers): 6.053 mg/L, EydwC50 (7 day, yield based on dry weight): 2.906 mg/L, ErdwC50 (7 day, growth rate based on dry weight): 6.206 mg/L. - Reported statistics and error estimates:
- The doubling time of frond number in the control was 2.24 days (less than 2.5 days). The validity criterion was within acceptable limit and therefore the study can be considered as valid.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test item Leuco Sulfur Blue 15 had no toxic effect at aquatic saturation on Lemna gibba; the EC10, EC50 and overall LOEC is higher than the nominal concentration of 100 mg/L of the test item in the test medium, which corresponds to the mean measured concentration of 1.69 mg/L, based on water accommodated fraction of the total product.
- Executive summary:
The influence of the test item on the growth of the freshwater aquatic plant Lemna gibba (duckweed) was investigated in a 7‑day static test, based on the OECD Guideline No. 221 “Lemna sp. Growth Inhibition Test” (2006) with nominal concentrations of 6.25, 12.5, 25, 50 and 100 mg product/L.
Based on the results the EC50 and NOEC for the test item were determined to be > 100 mg/L and 100 mg/L (nominal concentration, corresponding to the mean measured concentration of 1.69 mg/L), respectively.
All validity criteria were met and therefore the study can be considered as valid. All biological results are based on the mean measured test item concentrations of the total product.
Reference
Results of the Preliminary Range-finding Test
Nominal concentrations |
Control |
0.1 |
1 |
10 |
50 |
100 |
|||||||
Average number of fronds |
80.0 |
75.5 |
89.0 |
78.5 |
63.0 |
61.0 |
|||||||
Growth Rates (µ) |
0.283 |
0.275 |
0.297 |
0.281 |
0.249 |
0.245 |
|||||||
% Inhibition of µ |
- |
2.89 |
-4.78* |
0.92 |
12.17 |
13.67 |
* Negative value means growth increase
Calculation of Exposure Concentrations
Nominal |
Measuredconcentration(mg/L) |
Mean measuredconcentration |
|
Start of the Study |
End of the Study |
||
Control |
- |
- |
- |
6.25 (WAF*) |
<LOD** |
<LOD** |
0.10 |
12.5 (WAF*) |
0.28 |
0.32 |
0.30 |
25 (WAF*) |
0.55 |
0.56 |
0.55 |
50 (WAF*) |
0.94 |
0.89 |
0.91 |
100 (WAF*) |
1.82 |
1.57 |
1.69 |
- not detected
* water accommodated fraction (OECD No. 23.)
**test concentration measured < LOD (Limit of detection) was calculated as LOD(OECD No. 23.)
Growth rates (µ) and Percentage Inhibition ofµbased on Frond Number
Concentration |
Growth rate (µ) and % inhibition ofµ |
||
Nominal |
Measured |
0–168 h(based on frond number) |
|
µ |
% Iµ |
||
Control |
- |
0.310 |
- |
6.25 (WAF*) |
0.10 |
0.314 |
-1.35** |
12.5 (WAF*) |
0.30 |
0.307 |
0.69 |
25 (WAF*) |
0.55 |
0.314 |
-1.52** |
50 (WAF*) |
0.91 |
0.310 |
-0.11** |
100 (WAF*) |
1.69 |
0.308 |
0.54 |
* water accommodated fraction (OECD No. 23.)
** negative value indicates increase in comparison to the control
Growth rates (µ) and Percentage Inhibition ofµbased on Dry Weight
Concentration |
Growth rate (µ) and % inhibition ofµ |
||
Nominal |
Measured |
0–168 h(based on dry weight) |
|
µ |
% Iµ |
||
Control |
- |
0.3309 |
- |
6.25 (WAF*) |
0.10 |
0.3337 |
-0.86** |
12.5 (WAF*) |
0.30 |
0.3276 |
0.98 |
25 (WAF*) |
0.55 |
0.3368 |
-1.79** |
50 (WAF*) |
0.91 |
0.3239 |
2.10 |
100 (WAF*) |
1.69 |
0.3307 |
0.04 |
* water accommodated fraction (OECD No. 23.)
**negative value indicates increase in comparison to the control
Yield (y) and Percentage Inhibition of Yield based on Frond Number
Concentration |
Yield (y) and % inhibition of yield |
||
Nominal |
Measured |
0–168 h(based on frond number) |
|
y |
% Iy |
||
Control |
- |
85.17 |
- |
6.25 (WAF*) |
0.10 |
88.00 |
-3.33** |
12.5 (WAF*) |
0.30 |
83.67 |
1.76 |
25 (WAF*) |
0.55 |
88.33 |
-3.72** |
50 (WAF*) |
0.91 |
85.33 |
-0.20** |
100 (WAF*) |
1.69 |
84.00 |
1.37 |
* water accommodated fraction (OECD No. 23.)
** negative value indicates increase in comparison to the control
Yield (y) and Percentage Inhibition of Yield based on Dry Weight
Concentration |
Yield (y) and % inhibition of yield |
||
Nominal |
Measured |
0–168 h(based on dry weight) |
|
y |
% Iy |
||
Control |
- |
0.0062 |
- |
6.25 (WAF*) |
0.10 |
0.0064 |
-2.27** |
12.5 (WAF*) |
0.30 |
0.0061 |
2.54 |
25 (WAF*) |
0.55 |
0.0065 |
-4.67** |
50 (WAF*) |
0.91 |
0.0059 |
5.15 |
100 (WAF*) |
1.69 |
0.0062 |
0.08 |
* water accommodated fraction (OECD No. 23.)
** negative value indicates increase in comparison to the control
Symptoms, Changes ofLemna gibbaPlants Observed during the Test
Concentration |
3rdday of |
5thday of |
7thday of |
||||
Nominal |
Measured |
Symptoms |
Degree of change |
Symptoms |
Degree of change |
Symptoms |
Degree of change |
Control |
- |
n |
- |
n |
- |
n |
- |
6.25 (WAF*) |
0.10 |
n |
- |
n |
- |
n |
- |
12.5 (WAF*) |
0.30 |
n |
- |
n |
- |
n |
- |
25 (WAF*) |
0.55 |
n |
- |
n |
- |
n |
- |
50 (WAF*) |
0.91 |
n |
- |
n |
- |
n |
- |
100 (WAF*) |
1.69 |
n |
- |
n |
- |
n |
- |
* water accommodated fraction (OECD No. 23.)
Description of key information
The test item Leuco Sulfur Blue 15 had no toxic effect at aquatic saturation on Lemna gibba; the EC10, EC50 and overall LOEC is higher than the nominal concentration of 100 mg/L of the test item in the test medium, which corresponds to the mean measured concentration of 1.69 mg/L, based on water accommodated fraction of the total product.
Key value for chemical safety assessment
- EC10 or NOEC for freshwater plants:
- 1.69 mg/L
Additional information
The influence of the test item on the growth of the freshwater aquatic plant Lemna gibba (duckweed) was investigated in a 7‑day static test, based on the OECD Guideline No. 221 “Lemna sp. Growth Inhibition Test” (2006) with nominal concentrations of 6.25, 12.5, 25, 50 and 100 mg product/L.
Based on the results the EC50 and NOEC for the test item were determinedto be > 100 mg/L and 100 mg/L,respectively.
All validity criteria were met and therefore the study can be considered as valid. All biological results are based on the mean measured test item concentrations of the total product.
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