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EC number: 701-177-3 | CAS number: -
- 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 aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 30 May - 01 Jun 1989
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Version / remarks:
- adopted in 1982
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The stock solution contained 100 mg/L test item and 100 mg/L Tween 80 and was stirred for 60 min at 293 K. A serial dilution with dilution water was prepared and each test vessel received 10 mL of the respective dilution.
- Chemical name of vehicle: Tween 80 - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Water flea
- Strain: Straus
- Source: Laboratory breed at BASF, originally obtained in 1978 from the Institut National de Recherche Chimique Appliquée, France
- Age at study initiation (mean and range, SD): 2 - 24 h
ANIMAL HUSBANDRY
- Light: 16 h light/8 h dark, 5 µE/m2 x s, 400 - 750 nm
- Type and amount of food: Green algae
- Feeding frequency: Once daily - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 2.77 mmol/L
- Test temperature:
- 292.5 - 293.8 K
- pH:
- 7.77 - 8.14
- Dissolved oxygen:
- 8.36 - 8.87
- Nominal and measured concentrations:
- Nominal: 0, 0.098, 0.195, 0.39, 0.781, 1.56, 3.12, 6.25, 12.5, 25.0, 50.0 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Centrifuge glass vessels with flat bottom
- Material, fill volume: Glass, 10 mL
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Deionised water
- Ca/Mg ratio: 4:1
- Conductivity: 600 - 700 µS/cm
- Intervals of water quality measurement: Temperature, oxygen and pH were measured at test start and test end.
OTHER TEST CONDITIONS
- Light intensity: Diffuse light
EFFECT PARAMETERS MEASURED (with observation intervals if applicable)
- Immobilisation was recorded after 0, 3, 6, 24 and 48 h.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.0 - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.53 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 0.47 - 0.59
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- 0.39 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- 0.781 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Mortality of control: No mortality
- Immobilisation: 5% immobilisation at 0.39 mg/L, 100% immobilisation at 0.781 to 50 mg/L - Reported statistics and error estimates:
- Determination of EC50 (48h) by moving average method
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 21 Jul - 24 Jul 2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- adopted in 2004
- Deviations:
- yes
- Remarks:
- Higher temperature during the test (Guideline: 18 - 22 °C, Test: 23.5 - 23.7 °C)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Version / remarks:
- adopted in 2008
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Mainz, Germany
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: All concentrations were measured at test start and test end.
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A stock solution containing 10 g/L was prepared using the following procedure: 10 g test item was mixed with 1.1 g NaOH (45%). 40 mL deionised water (80 – 100 °C) was added. After homogenisation with a glass stirrer, 85 mL deionised water (room temperature) was added. Then, the vessel was stirred on a magnetic stirrer. 0.5 M NaOH was added until the resulting solution was clear. The pH of the solution was adjusted to 7.8 ± 0.2 with 1 M HCl. the solution was transferred into a volumetric flask and filled up to 1000 mL with deionised water. From this solution, the concentrations to be tested were prepared by diluting with dilution water. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Water flea
- Strain: Straus
- Source: Umweltbundesamt Berlin, Germany, received on 27 Sep 2007
- Age at study initiation (mean and range, SD): < 24 h
- Feeding during test: None
ANIMAL HUSBANDRY
- Method of breeding: Daphnia magna is bred in the LAUS GmbH throughout the year. The animals are kept in 2L glass beakers in M4 medium and multiply by parthenogenesis thus being genetically identical.
- Type and amount of food: Unicellular green algae
- Feeding frequency: Twice a week - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 250 mg CaCO3/L
- Test temperature:
- 23.2 - 23.7 °C
- pH:
- 7.3 - 7.8
- Dissolved oxygen:
- 6.4 - 8.3 mg/L
- Nominal and measured concentrations:
- Nominal: 0, 0.1, 0.22, 0.46, 1.0, 2.2, 4.6, 10, 22, 46, 100 mg/L
Mean measured: < LOQ, < LOQ, < LOQ, < LOQ, 0.42, 0.60, 1.77, 5.58, 12.14, 28.94, 64.70 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel: Beakers
- Material, size, fill volume: Glass, 50 mL, 20 mL
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Deionised water was used for the preparation of M4 medium
- Culture medium different from test medium: no
- Intervals of water quality measurement: pH and oxygen concentration were measured at test start and test end.
OTHER TEST CONDITIONS
- Photoperiod: Darkness
EFFECT PARAMETERS MEASURED (with observation intervals if applicable)
- After 24 and 48h the immobilised daphnia were counted.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.2 - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.43 mg/L
- Nominal / measured:
- meas. (geom. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.38 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Mortality of control: 5% after 48 h
- Immobilisation: 10% at nominal 0.46 mg/L, 70% at nominal 1.0 mg/L, 100% at nominal 2.2 mg/L to 100 mg/L
- Analytical measurements: In treatments 0.1 – 0.46 mg/L (nominal) no test item was detectable after 48 h. The recovery after 48 h in treatments 1 – 100 mg/L (nominal) was in the range of 44 – 128% of the start concentration. Because of the medium correlation between nominal and measured concentrations, the determination of the biological results was based on the geometric mean of the measured concentrations for treatments 1 – 100 mg/L (nominal) and on the measured concentration at test start for treatment 0.46 mg/L (nominal, measured: 0.38 mg/L). Treatments 0.1 and 0.22 mg/L were not used for the evaluation of the results. - Results with reference substance (positive control):
- - The reference test was carried out 08 - 09 Jun 2010
- EC50 (24h): 1.6 mg/L, 95% CL = 1.4 - 1.9 mg/L
- NOEC (24h): 1.0 mg/L - Validity criteria fulfilled:
- yes
Referenceopen allclose all
Table 1: Immobilisation of Daphnia magna
Concentration (mg/L) |
Mobile Daphnia after |
||
0 h |
24 h |
48 h |
|
0 |
20 |
20 |
20 |
0.098 |
20 |
20 |
20 |
0.195 |
20 |
20 |
20 |
0.39 |
20 |
20 |
19 |
0.781 |
20 |
7 |
0 |
1.56 |
20 |
0 |
0 |
3.12 |
20 |
0 |
0 |
6.25 |
20 |
0 |
0 |
12.5 |
20 |
0 |
0 |
25.0 |
20 |
0 |
0 |
50.0 |
20 |
0 |
0 |
Immobilities Exp. 1
Nominal Conc. In mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
abs. |
in % |
abs. |
in % |
|||||||
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1.0 |
3 |
3 |
4 |
2 |
60 |
4 |
4 |
4 |
2 |
70 |
2.2 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
4.6 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
10 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
22 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
46 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
100 |
5 |
5 |
5 |
5 |
100 |
5 |
5 |
5 |
5 |
100 |
Immobilities Exp. 2
Nominal Conc. In mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
abs. |
in % |
abs. |
in % |
|||||||
0 |
1 |
0 |
0 |
0 |
5 |
1 |
0 |
0 |
0 |
5 |
0.1 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0.22 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0.46 |
0 |
0 |
0 |
0 |
0 |
1 |
1 |
0 |
0 |
10 |
Measured concentrations
Nominal Conc. in mg/L |
Measured Conc. in mg/L |
% Recovery after 48h |
% of Nominal Conc. |
Geom. Mean in mg/L |
||
0 h |
48 h |
|
0 h |
48 h |
|
|
0 |
n.d. |
n.d. |
- |
- |
- |
- |
0.1 |
0.36 |
n.d. |
0 |
363 |
-- |
-- |
0.22 |
0.37 |
n.d. |
0 |
166 |
-- |
-- |
0.46 |
0.38 |
n.d. |
0 |
82 |
-- |
-- |
1 |
0.51 |
0.35 |
70 |
51 |
35 |
0.42 |
2.2 |
0.90 |
0.40 |
44 |
41 |
18 |
0.60 |
4.6 |
2.20 |
1.43 |
65 |
48 |
31 |
1.77 |
10 |
5.80 |
5.36 |
93 |
58 |
54 |
5.58 |
22 |
12.65 |
11.64 |
92 |
58 |
53 |
12.14 |
46 |
27.02 |
30.99 |
115 |
59 |
67 |
28.94 |
100 |
57.21 |
73.17 |
128 |
57 |
73 |
64.70 |
n.d. = not detectable
Description of key information
EC50 (48h) = 0.43 mg/L for Daphnia magna (OECD 202)
Key value for chemical safety assessment
Additional information
Two studies investigating the short-term toxicity of N-methyl-N-(C18-(unsaturated)alkanoyl)glycine (EC 701-177-3) to aquatic invertebrates are available.
The key study was carried out according to OECD guideline 202 and GLP including analytical measurement. Daphnia magna was exposed to the following ten nominal concentrations 0.1, 0.22, 0.46, 1.0, 2.2, 4.6, 10, 22, 46, 100 mg/L under static conditions. These test concentrations were performed in two different tests. The first test was conducted using seven test concentrations (nominal: 1.0, 2.2, 4.6, 10, 22, 46, 100 mg/L). As immobilization (≥ 70%) was observed in all test concentrations, a second test was performed using three additional concentrations (nominal: 0.1, 0.22, 0.46 mg/L). Analytical measurements verified the test item concentration to be 44 – 128% of the initial test concentrations of 1 – 100 mg/L throughout the exposure period, 82 – 363% for the initial test concentrations of 0.1 – 0.46 mf/L. For the test concentrations 0.1 - 0.46 mg/L after 48 h test concentrations of < LOD are detectable. Immobility could be observed in concentrations ≥ 1 mg/L (nominal).The test revealed an EC50 (48h) of 0.43 mg/L (measured).
The supporting study was carried out under non-GLP conditions according to EU Method C.2 and without analytical measurement. Daphnia magna was exposed to ten test concentrations (0.098, 0.195, 0.39, 0.781, 1.56, 3.12, 6.25, 12.5, 25.0, 50.0 mg/L) under static conditions. Immobility of 100% could be observed in concentrations ≥ 0.781 mg/L. An EC50 (48h) of 0.53 mg/L (nominal) is reported.
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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