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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 257-104-6 | CAS number: 51277-96-4
- 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 algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2015-04-19 to 2015-04-28
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Version / remarks:
- 2011
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- All test item concentrations and the control were analytically verified via LC-MS/MS at the beginning, after 24, 48 hours and at the end of the test. Samples at test start were taken from an additional replicate without algae. For the test item analysis after 24, 48 and 72 hours the test samples were taken from the pooled test replicates per concentration level and control.
- Sample storage conditions before analysis: room temperature - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
A stock solution of 10 mg test item/L was prepared with test medium (natural river water). This solution was stirred at a temperature of 40°C ± 2°C for 24 ± 1 hours. Thereafter, the saturated solution was stirred for further 24 ± 1 hours and cooled down to the temperature of the test (21 - 24°C).
5 concentration levels in a geometrical series with a separation factor of √10, prepared by diluting the stock solution of 10 mg test item/L with test medium, were tested as follows: 0.514 – 1.08 – 2.26 – 4.76 – 10.0 mg/L. As the test item is a solid with a content of ca. 96 % the test concentrations of the pure substance were: 0.493 – 1.04 – 2.17 – 4.57 – 9.60 mg pure compound/L. - Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Common name: green algae
- Strain: Desmodesmus subspicatus CHODAT SAG 86.81
- Source (laboratory, culture collection): Sammlung von Algenkulturen (SAG), Pflanzenphysiologisches Institut der Universität Göttingen, Nikolausberger Weg 18, D-37073 Göttingen
- Age of inoculum (at test initiation): two days old preculture
- Method of cultivation: Fresh stocks were prepared every month on Z-Agar. Light intensity amounted to 35 - 70 µE•m-2•s-1 for 24 h per day. Nutrient medium Z according to LÜTTGE et al. (1994) - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Test temperature:
- 22.5 (22.0 - 23.0) °C
- pH:
- start: 8.02 - 8.06; end: 7.87 - 8.01
- Nominal and measured concentrations:
- nominal: 0.493, 1.04, 2.17, 4.57, 9.60 mg a.i./L
measured (geom. mean): 0.0210, 0.0347, 0.133, 2.33, 8.37 mg a.i./L - Details on test conditions:
- TEST SYSTEM
- Test vessel: Sterile Erlenmeyer flasks, volume: 250 mL, provided with cotton wool plugs. The test container were pretreated with the appropriate test solutions for 72 hours under test conditions. Before the start of the exposure phase, the test container were emptied and refilled with freshly prepared test solutions.
- Fill volume: 100 mL
- Initial cells density: nominal: approximately 2 - 5 x 1E03 cells/mL; current: 4998 cells/mL
- Control end cells density: 696778 (mean)
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 6
GROWTH MEDIUM
- Standard medium used: no, natural river water, for details see section "any other information on materials and methods"
TEST MEDIUM / WATER PARAMETERS
river water as specified in section "any other information on materials and methods"
OTHER TEST CONDITIONS
- Sterile test conditions: The natural river water was stored at 15 ± 2 °C and at - 18± 2 °C for at least 24 hours. Freezing was found to be suitable to minimize the content of vital natural algae cells of the water as well as to reduce microbial (bacterial) activity
- Adjustment of pH: no
- Photoperiod: 24 hours/day light
- Light intensity and quality: 60 - 120 µE • m-2 • s-1
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Chlorophyll measurement: Chlorophyll a-fluorescence, excitation at 436 nm, emission at 685 nm
TEST CONCENTRATIONS
- Spacing factor for test concentrations: sqrt(10)
Range finding study
- Test concentrations: 0.096, 0.96, 9.6, 96 mg a.i./L, nominal, prepared in natural river water
- Results used to determine the conditions for the definitive study:
Growth Rate Inhibition: 100, 100, 10, -2% at 0.096, 0.96, 9.6, 96 mg a.i./L
Yield Inhibition: 100, 100, 43, -11% at 0.096, 0.96, 9.6, 96 mg a.i./L - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.02 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 0.205 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Remarks on result:
- other: 95% c.l. 0.131 - 0.881 mg/L
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.407 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- growth rate
- Remarks on result:
- other: 95% c.l. 0.213 -1.12 mg/L
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.02 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- < 0.02 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.252 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- act. ingr.
- Basis for effect:
- biomass
- Remarks on result:
- other: 95% c.l. 0.103 - 0.892 mg/L
- Details on results:
- - Exponential growth in the control (for algal test): yes
- Observation of abnormalities (for algal test): Microscopic evaluation of the cells at start and the end of the incubation period revealed nomorphological abnormalities. - Results with reference substance (positive control):
- - Results with reference substance valid?
- ErC50: 0.586 (95% c.l. 0.522 - 0.818mg/L); valid range: 0.678 ± 0.414
- EyC50: 0.401 (95% c.l. 0.285 - 0.469), valid range: 0.319 ± 0.141
- Other: tested from 2014-10-14 to 2014-10-17 - Reported statistics and error estimates:
- EC10-, EC20- and EC50-values of the growth rate and yield inhibition after 72 hours were calculated by sigmoidal dose-response. Calculation of the confidence intervals EC10-, EC20- and EC50-values were carried out using standard procedures.
The values for NOEC/LOEC were determined by calculation of statistical significance of inhibition of growth rate and yield. As standard methods, One Way Analysis of Variance (ANOVA) and DUNNETT’s test were used for NOEC/LOEC calculations. When running a One Way Analysis of Variance, a Normality test and an Equal Variance test were done first. P-values for both Normality and Equal Variance tests are 0.05. The alpha-value (acceptable probability of incorrectly concluding that there is a difference) is 0.05. Equal Variance test failed for yield. To pass the Equal Variance test, the two highest concentrations were excluded from statistical evaluation. - Validity criteria fulfilled:
- yes
- Conclusions:
- The NOEC, EC10 and EC50 of C16 Alkylamidopropyltrimethylammonium Chloride to the green alga Desmodesmus subspicatus based on growth rate were 0.0202 mg a.i./L, 0.205 mg a.i./L (95% c.l. 0.131 – 0.881 mg a.i./L) and 0.407 mg a.i./L (95% c.l. 0.213 – 1.12 mg a.i./L), respectively. All values given are based on the geometric mean exposure concentrations.
- Executive summary:
In a 72 hour toxicity study according to OECD Guideline 201 (2011), the cultures of Desmodesmus subspicatus CHODAT SAG 86.81 were exposed to C16 Alkylamidopropyltrimethylammonium Chloride at nominal concentrations of 0 (control), 0.493, 1.04, 2.17, 4.57, 9.60 mg a.i./L in natural river water, corresponding to geom. mean measured concentrations of 0 (control), 0.0210, 0.0347, 0.133, 2.33, 8.37 mg a.i./L under static conditions.
The test item is known to sorb to organic and inorganic materials by different mechanisms. The sorption processes are mostly non-linear, means are concentration dependent. Due to these properties the test item is difficult to test in synthetic water (e.g. sorption to the test organisms and glass walls of the test vessels) and results from such tests depend from the test settings applied.Therefore, natural river water was usedwhich contains particulate as well as dissolved organic carbon to which the test item can sorb partially to reduce the difficulties encountered in tests with synthetic water (e.g. preventing that the test item settles onto surfaces). The sorbed fraction of the test item is difficult to extract from the test system which normally leads to low analytical recoveries at the end of the exposure. Nevertheless the test item is present in the test system and therefore available for exposure (dissolved in water and sorbed).
Additionally, the test vessels were pre-treated with the test solutions one day before the start of the respective exposure interval to saturate the glass walls with sorbed test item in the definitive test.This procedure was carried out to achieve stable exposure concentrations in the test vessels and to reduce losses of the test item by adsorption onto the glass walls.All test concentrations and the control were analytically verified by LC-MS/MS analysis at the start of the exposure (0 hours), 24, 48 hours and the end of the exposure (72 hours).
The measured concentrations of the test item at the start of the exposure were in the range of 82 to 100 % of the nominal values. After 24 h, the measured concentrations of the test item were in the range of 22 to 76 % of the nominal values. After 48 h, the measured concentrations of the test item were in the range of < LOQ to 87 % of the nominal values and at the end of the exposure, the measured concentrations of the test item were in the range of< LOQto 96 % of the nominal values. Therefore, all values given are based on the geometric mean exposure concentrations.
The NOEC, EC10 and EC50 based on growth rate inhibition were0.0202 mg a.i./L, 0.205 mg a.i./L (95% c.l. 0.131 – 0.881 mg a.i./L) and 0.407 mg a.i./L (95% c.l. 0.213 – 1.12 mg a.i./L), respectively.
The % growth inhibition in the treated algal culture as compared to the control ranged from 2% to 100%.
The NOEC, EC10 and EC50 based on yield were0.0202 mg a.i./L, < 0.0202 mg a.i./L and 0.252 mg a.i./L (95% c.l. 0.103 – 0.892 mg a.i./L), respectively.
Microscopic evaluation of the cells at start and the end of the incubation period revealed no morphological abnormalities.
This toxicity study is classified as acceptable and satisfies the guideline requirements for the algal growth inhibition test in Desmodesmus subspicatus.
Results Synopsis
Test Organism: Desmodesmus subspicatus CHODAT SAG 86.81
Test Type: Static
72 hr ErC10: 0.205mg a.i./L,(95% c.l. 0.131 – 0.881 mg a.i./L)
72 hr ErC50: 0.407 mg a.i./L (95% c.l. 0.213 – 1.12 mg a.i./L)
72 hr NOEC: 0.0202 mg a.i./L
Endpoint(s) Effected: growth rate
72 hr ErC10: < 0.0202mg a.i./L
72 hr ErC50: 0.252 mg a.i./L (95% c.l. 0.103 – 0.892 mg a.i./L)
72 hr NOEC: 0.0202 mg a.i./L
Endpoint(s) Effected: yield
Reference
Validity Criterion |
Required |
This study |
Increase of the cell growth in the control (72 hours) |
Exponentially > 16-fold corresponding to a specific growth rate of 0.92 / day |
139-fold (specific growth rate 1.64 / day) |
Mean coefficients of variation for section-by-section specific growth rates (days 0-1, 1-2 and 2-3) in the control cultures |
< 35 % |
18.3 % |
Coefficient of variation of average specific growth rates during the whole test period in replicate control cultures |
< 7 % |
2.22 % |
Cell Densities
Geometric mean exposure test item concentration |
Replicate |
Cell density [cells/mL] |
|||
[mg/L] |
No. |
0 hours |
24 hours |
48 hours |
72 hours |
8.37 |
1 |
4998 |
<LOQ |
<LOQ |
<LOQ |
2 |
4998 |
<LOQ |
<LOQ |
<LOQ |
|
3 |
4998 |
<LOQ |
<LOQ |
<LOQ |
|
Mean |
4998 |
n.a. |
n.a. |
n.a. |
|
2.33 |
1 |
4998 |
3162 |
<LOQ |
<LOQ |
2 |
4998 |
3183 |
<LOQ |
<LOQ |
|
3 |
4998 |
4531 |
<LOQ |
<LOQ |
|
Mean |
4998 |
3625 |
n.a. |
n.a. |
|
0.133 |
1 |
4998 |
17425 |
146721 |
649803 |
2 |
4998 |
19427 |
135580 |
605795 |
|
3 |
4998 |
24118 |
153443 |
620349 |
|
Mean |
4998 |
20323 |
145248 |
625316 |
|
0.0347 |
1 |
4998 |
20761 |
102154 |
407455 |
2 |
4998 |
20237 |
98806 |
360588 |
|
3 |
4998 |
21904 |
105312 |
478535 |
|
Mean |
4998 |
20967 |
102091 |
415526 |
|
0.0210 |
1 |
4998 |
24507 |
169864 |
484816 |
2 |
4998 |
22220 |
191123 |
667475 |
|
3 |
4998 |
27388 |
139322 |
562610 |
|
Mean |
4998 |
24705 |
166770 |
571634 |
|
Control |
1 |
4998 |
22589 |
152625 |
643002 |
2 |
4998 |
17044 |
126423 |
582664 |
|
3 |
4998 |
24252 |
211299 |
777582 |
|
4 |
4998 |
19444 |
147440 |
685884 |
|
5 |
4998 |
24395 |
143190 |
735307 |
|
6 |
4998 |
26387 |
185661 |
756228 |
|
Mean |
4998 |
22352 |
161106 |
696778 |
Evaluation after 72 hours:Statistically significant differences of growth rates and yield compared to control values are marked (+), not significant differences are marked (-).
n.a. = not applicable
Geometric mean exposure test item concentration [mg/L] |
Replicate No. |
Growth rate [d-1] |
Growth rate inhibition [%] |
Yield [cells/mL] |
Inhibition of yield [%] |
||||||
8.37 |
1 2 3 Mean |
n.a. n.a. n.a. n.a. |
100 100 100 100 |
n.a. n.a. n.a. n.a. |
100 100 100 100 |
||||||
2.33 |
1 2 3 Mean |
n.a. n.a. n.a. n.a. |
100 100 100 100 |
n.a. n.a. n.a. n.a. |
100 100 100 100 |
||||||
0.133 |
1 2 3 Mean |
1.62 1.60 1.61 1.61 (-) |
1 3 2 2 |
644805 600797 615351 620318 (-) |
7 13 11 10 |
||||||
0.0347 |
1 2 3 Mean |
1.47 1.43 1.52 1.47(+) |
11 13 8 11 |
402457 355590 473537 410528 (+) |
42 49 32 41 |
||||||
0.0210 |
1 2 3 Mean |
1.53 1.63 1.58 1.58 (-) |
11 13 8 11 |
479818 662477 557612 566636 (-) |
31 4 19 18 |
||||||
Control |
1 2 3 4 5 6 Mean |
1.62 1.59 1.68 1.64 1.66 1.67 1.64 |
|
638004 577666 772584 680886 730309 751230 691780 |
|
Description of key information
72 h NOEC (growth rate) = 0.0202 mg a.i./L
72 h ErC10 = 0.205 mg a.i./L (95% c.l. 0.131 – 0.881 mg a.i./L)
72 h ErC50 = 0.407 mg a.i./L (95% c.l. 0.213 – 1.12 mg a.i./L) (geom. mean measured);
Desmodesmus subspicatus, static, river water; OECD Guideline 201 (2011); RL1; GLP
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 0.407 mg/L
- EC10 or NOEC for freshwater algae:
- 0.205 mg/L
Additional information
In a 72 hour toxicity study according to OECD Guideline 201 (2011), the cultures of Desmodesmus subspicatus CHODAT SAG 86.81 were exposed to C16 Alkylamidopropyltrimethylammonium Chloride at nominal concentrations of 0 (control), 0.493, 1.04, 2.17, 4.57, 9.60 mg a.i./L in natural river water, corresponding to geom. mean measured concentrations of 0 (control), 0.0210, 0.0347, 0.133, 2.33, 8.37 mg a.i./L under static conditions.
The test item is known to sorb to organic and inorganic materials by different mechanisms. The sorption processes are mostly non-linear, means are concentration dependent. Due to these properties the test item is difficult to test in synthetic water (e.g. sorption to the test organisms and glass walls of the test vessels) and results from such tests depend from the test settings applied.Therefore, natural river water was usedwhich contains particulate as well as dissolved organic carbon to which the test item can sorb partially to reduce the difficulties encountered in tests with synthetic water (e.g. preventing that the test item settles onto surfaces). The sorbed fraction of the test item is difficult to extract from the test system which normally leads to low analytical recoveries at the end of the exposure. Nevertheless the test item is present in the test system and therefore available for exposure (dissolved in water and sorbed).
Additionally, the test vessels were pre-treated with the test solutions one day before the start of the respective exposure interval to saturate the glass walls with sorbed test item in the definitive test.This procedure was carried out to achieve stable exposure concentrations in the test vessels and to reduce losses of the test item by adsorption onto the glass walls.All test concentrations and the control were analytically verified by LC-MS/MS analysis at the start of the exposure (0 hours), 24, 48 hours and the end of the exposure (72 hours).
The measured concentrations of the test item at the start of the exposure were in the range of 82 to 100 % of the nominal values. After 24 h, the measured concentrations of the test item were in the range of 22 to 76 % of the nominal values. After 48 h, the measured concentrations of the test item were in the range of < LOQ to 87 % of the nominal values and at the end of the exposure, the measured concentrations of the test item were in the range of< LOQto 96 % of the nominal values. Therefore, all values given are based on the geometric mean exposure concentrations.
The NOEC, EC10 and EC50 based on growth rate inhibition were 0.0202 mg a.i./L, 0.205 mg a.i./L (95% c.l. 0.131 – 0.881 mg a.i./L) and 0.407 mg a.i./L (95% c.l. 0.213 – 1.12 mg a.i./L), respectively.
The % growth inhibition in the treated algal culture as compared to the control ranged from 2% to 100%.
The NOEC, EC10 and EC50 based on yield were 0.0202 mg a.i./L, < 0.0202 mg a.i./L and 0.252 mg a.i./L (95% c.l. 0.103 – 0.892 mg a.i./L), respectively.
Microscopic evaluation of the cells at start and the end of the incubation period revealed no morphological abnormalities.
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.