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Diss Factsheets

Ecotoxicological information

Toxicity to aquatic algae and cyanobacteria

Administrative data

Endpoint:
toxicity to aquatic algae and cyanobacteria
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1997
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Well documented report of a guideline study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1997
Report date:
1997

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 201 (Alga, Growth Inhibition Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Acrylamide
EC Number:
201-173-7
EC Name:
Acrylamide
Cas Number:
79-06-1
Molecular formula:
C3H5NO
IUPAC Name:
Prop-2-enamide
Details on test material:
- Name of test material (as cited in study report): ACRYLAMIDE 50 ST
- Substance type: organic
- Physical state: Colourless liquid
- Composition of test material, percentage of components: 50% in aqueous solution.
- Lot/batch No.: 5069
- Storage condition of test material: In dakness and room temperatue.

Sampling and analysis

Analytical monitoring:
no

Test solutions

Vehicle:
no

Test organisms

Test organisms (species):
Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
Details on test organisms:
TEST ORGANISM
- Common name: Green Algae
- Strain: Selenastrum capricornutum (CCAP 278/4)
- Source (laboratory, culture collection): AQUARIUM DE TROUVILLE (17 rue de Paris, 14360 TROUVILLE).
- Age of inoculum (at test initiation): approximately 72-hours
- Method of cultivation: the sub-culture used for the algal inoculation was made in the same culture medium as that used for the test, and kept under the same conditions as those employed for the test (culture medium, lighting, temperature, sting). Contemporaneously to the start of the test, pre-culture cell concentration was measured and the volume to be used for the inoculation of test and control media was determined.
ACCLIMATION
- Acclimation period: none reported
- Culturing media and conditions: same as test
- Any deformed or abnormal cells observed: none reported

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
72 h

Test conditions

Hardness:
40 mg/L
Test temperature:
24.0-24.5°C
pH:
6.95-8.84
Dissolved oxygen:
Not reported
Nominal and measured concentrations:
Nominal : 10, 18, 32, 56 and 100 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel:
- Type: open
- Material, size, headspace, fill volume: Erlenmeyer flasks of 250 ml capacity, provided with a cotton-wool plug.
- Aeration: no
- Initial cells density: 9,600 cells per millilitre
- Control end cells density: 3,263,333 per millilitre
- No. of vessels per concentration (replicates): 3
- No. of vessels per vehicle control (replicates): 3
GROWTH MEDIUM and TEST MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: sterile tap water
- Culture medium different from test medium: No
- Total organic carbon: 0 mg/l
- Particulate matter: 0 mg/l
- Salts: Ca(NO3)2.4 H2O = 40mg/L; KNO3 = 100mg/L, MgSO4.7 H2O = 30Mg/L; K2HPO4 = 40mg/L; CuSO4.5 H2O = 0.015mg/L; (NH4)6.Mo7O24.4 H2O = 0.030mg/L; ZnSO4.7 H2O = 0.030mg/L; CoCl2.6 H2O = 0.030mg/L; Mn(NO3)2.4 H2O = 0.030mg/L; C6H8O7.H20 = 0.030mg/L; H3BO3 = 0.030mg/L; Ammonium iron III citrate (Fe2O3 content = 29-32 %) = 0.8125mg/L; FeSO4.7 H2O = 0.3125mg/L; FeCl3.6 H2O = 0.3125mg/L
- Pesticides: none
- Chlorine: none reported
- Alkalinity: not reported
- Ca/mg ratio: not reported
- Conductivity: not reported
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Adjustment of pH: readjusted with HCl 0.1N.
- Photoperiod: continuous white lighting
- Light intensity and quality: artificial lighting 7180 - 7230 lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations:24 ,48 and 72 hours after the start of the test, the cell concentration was measured for each control and test flask by direct counting of cells with microscope.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 10, 18, 32, 56 and 100 mg
Reference substance (positive control):
no

Results and discussion

Effect concentrationsopen allclose all
Duration:
72 h
Dose descriptor:
IC50
Effect conc.:
67.7 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
biomass
Duration:
72 h
Dose descriptor:
IC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
growth rate
Duration:
72 h
Dose descriptor:
NOEC
Effect conc.:
32 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
biomass
Duration:
72 h
Dose descriptor:
NOEC
Effect conc.:
56 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
growth rate

Any other information on results incl. tables

Inhibitions íif the growth in comparison with the control group (lA as %)

 Test substace nomina! concentration (mg/L)   Inhibition of the cell growth (IA ) in 72 hours %
 10  -30
 18  - 18
 32  - 15
 56   43
 100   64

IA (%) = [(A control - A concentration) / A control] x 100

Inhibitions of the growth rate in comparison with the control group (lµ., as %)

 Test substace nominal concentration (mg/L)  Inhibition of the growth rate (Iµ) in 72 hours ( %)
10  -5
 18  -3
 32  -2
 56  14
100   26

Iµ (%) = [(µ control - µ concentration) / µ control ] x 100

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Remarks:
Cell concentration in the control group increased by a factor of at least 16 within 3 days as required: It increased by a factor of 340 during the test period.
Conclusions:
Under the test conditions the ICA50 (growth inhibition) of ACRYLAMIDE 50 ST to green algae Selenastrum capricornutum was 67.7 mg/l and the ICµ50 (growth rate inhibition) was greater than 100 mg/l. The No Observed Effect Concentration (NOEC) = 32 mg/l. These results are valid for the registered substance.