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EC number: 209-812-1 | CAS number: 593-84-0
- 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:
- key study
- Study period:
- 2000-04-12 to 2000-05-04
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- 194-04-04
- Deviations:
- no
- GLP compliance:
- no
- Remarks:
- The study described in this report was conducted in accordance with SN EN 45001.
- Specific details on test material used for the study:
- Batch 1210.9225
- Analytical monitoring:
- no
- Remarks:
- No chemical analyses of the test media were conducted. For the calculation of the effective concentrations, the nominal contents of the test solutions were use, assuming the test compound to be stable in water over 48 h.
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
Prior to the test, a batch of reconstituted water was aerated vigorously over a period of 2h. Final test concentrations were prepared with this aerated water by dilution of stock solutions of the test substance. 2 h before the test, vessels were filled with the formulated media to allow equilibration of pH, oxygen and temperature. Daphnia, which had been selected in size, were acclimatized to the reconstituted water for 4 hours before introduction into the test media. The pH was not adjusted before the test. Based on the results of a range finding test, nominal concentrations of the test substance forming a geometric series were added to the test media. A blank of test medium without test substance or other additives served as a control. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain/clone: Daphnia magna (Straus, 1820)
- Source: no data
- Age of parental stock (mean and range, SD): no data
- Feeding during test: no data
- Food type: 15 g sera micropan homogenized in 1L deionized water
- Frequency: Once a day, except weekends.
ACCLIMATION
- Acclimation period: 4 h
- Acclimation conditions (same as test or not): same
- Type and amount of food: no data
- Feeding frequency: no data
- Health during acclimation (any mortality observed): no data
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 20.0 (± 0.5) °C
- pH:
- 7.9 - 8.0
- Dissolved oxygen:
- 6.5 - 7.0 mg/l
- Salinity:
- no data
- Conductivity:
- no data
- Nominal and measured concentrations:
- Nominal concentrations:
0.25, 12.5, 25,.0, 50.0, 75.0, 100.0 mg/l - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml flasks, all-glass, with 50 ml of test medium
- Aeration: not aerated
- No. of organisms per vessel: 20
- No. of vessels per concentration (replicates): 2
- No. of vessels per control (replicates): 2
TEST MEDIUM / WATER PARAMETERS
Continuously aerated reconstituted water (ISO 6341 (3)); prepared with distilled water (conductivity <1.5 I-lS/cm).
The final test medium contained 25 mill of each of the following 4 stock solutions:
CaCI2 x 2 H20, 11.76 g/l; MgS04 x 7 H2O, 4.93 g/l; NaHCOs, 2.59 g/l; KCI, 0.23 g/l.
The sum of the Ca and Mg ions in this solution is 2.5 mmol/l.
The ratio of Ca:Mg ions is 4:1 and of Na:K ions is 10:1.
The total alkalinity of this solution is 0.8 mmol/l
OTHER TEST CONDITIONS
- Adjustment of pH: The pH was not adjusted before the test.
- Photoperiod: 16 h photoperiod a day, supplied by overhead white fluorescent tubes
- Light intensity: no data
EFFECT PARAMETERS MEASURED: Observations of immobile Daphnia were made after 24 and 48 h of exposure.
VEHICLE CONTROL PERFORMED: no
RANGE-FINDING STUDY
- Test concentrations: 1,10 and 100 mg/I
- Results used to determine the conditions for the definitive study:
Based on the data of the range finding test nominal concentrations with a spacing factor of 2 of 6.25, 12.5, 25, 50 and 100 mg/I and additionally 75 mg/I
were chosen for the definitive test. - Reference substance (positive control):
- no
- Remarks:
- Periodically conducted reference test with potassium dichromate.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 42.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 95 % confidence limits: 32.4-57.5 mg/I
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 77.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 95 % confidence limits: 66.1-95.5 mg/I)
- Details on results:
- The experimentally determined no-effect concentration (NOEC, ECo) was 12.5 and 6.25 mg/I after an exposure of 24 and 48 h, respectively.
- Reported statistics and error estimates:
- The coefficients (r2) of the regression curves for the 24 and 48 h observations were 0.950 and 0.878, respectively.
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the immobilization data the nominal median effect concentration (EC50) of Guanidine thiocyanate to Daphnia magna for 48 h was calculated to be 42.4 mg/I (95 % confidence limits: 32.4-57.5 mg/I).
- Executive summary:
The 48h-acute toxicity of Guanidine thiocyanate to Daphnia magna was studied under static conditions. Daphnids were exposed to control, and test chemical at (nominal) concentration of 0.25, 12.5, 25, 50.0, 75.0, 100.0 mg/l for 48 hr. Immobilization effects were observed daily. The 24 and 48 – hour EC50was 24 and 48 h was calculated to be 77.2 mg/l (95 % confidence limits: 66.1-95.5 mg/l) and 42.4 mg/l (95 % confidence limits: 32.4-57.5 mg/l), respectively.
The experimentally determined no-effect concentration (NOEC, EC0) based on immobilization was 12.5 and 6.25 mg/l after an exposure of 24 and 48 h, respectively.
This study is classified as acceptable and satisfies the guideline requirements for an acute toxicity study with freshwater invertebrates.
Results Synopsis
Test Organism: Daphnia magna < 2 mm
Test Type: Static
NOEL 48h: 6.25 mg/l (nominal) experimentally determined
EC50 48h: 42.4 mg /l (nominal) 95% C.I.: 32.4 - 57.5mg/I (nominal)
Endpoint(s) Effected: mobility
Reference
Definitive test: Immobilization of Daphnia magna after 24 and 48 h of exposure to the test material:
Nominal concentration (mg/I) |
Code |
Number of individuals per test vessel |
Immobile Daphnia (No./vessel) 24 h |
Immobile Daphnia (No./vessel) 48 h |
% immobile Daphnia after 24 h of exposure |
% immobile Daphnia after 48 h of exposure |
Control |
A |
20 |
0 |
0 |
0 |
0 |
0.0 |
B |
20 |
0 |
0 |
0 |
0 |
|
C |
20 |
0 |
1 |
0 |
5 |
6.25 |
A |
20 |
0 |
0 |
0 |
0 |
|
B |
20 |
0 |
0 |
0 |
0 |
12.5 |
A |
20 |
0 |
1 |
0 |
5 |
|
B |
20 |
1 |
4 |
5 |
20 |
25 |
A |
20 |
4 |
6 |
20 |
30 |
|
B |
20 |
4 |
5 |
20 |
25 |
50 |
A |
20 |
6 |
8 |
30 |
40 |
|
B |
20 |
7 |
7 |
35 |
35 |
75 |
A |
20 |
9 |
13 |
45 |
65 |
|
B |
20 |
11 |
15 |
55 |
75 |
100 |
A |
20 |
11 |
19 |
55 |
95 |
|
B |
20 |
12 |
17 |
60 |
85 |
Description of key information
The 48h-acute toxicity of Guanidine thiocyanate to aquatic invertebrates (Daphnids) was studied. The 48h-EC50 based on immobilization was found to be 42.4 mg/l (nominal, 100 % a.i.).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- 42.4 mg/L
Additional information
The 48h-acute toxicity of Guanidine thiocyanate to Daphnia magna was studied under static conditions. Daphnids were exposed to control, and test chemical at (nominal) concentration of 0.25, 12.5, 25, 50.0, 75.0, 100.0 mg/l for 48 hr. Immobilization effects were observed daily. The 24 and 48 – hour EC50was 24 and 48 h was calculated to be 77.2 mg/l (95 % confidence limits: 66.1-95.5 mg/l) and 42.4 mg/l (95 % confidence limits: 32.4-57.5 mg/l), respectively.
The experimentally determined no-effect concentration (NOEC, EC0) based on immobilization was 12.5 and 6.25 mg/l after an exposure of 24 and 48 h, respectively.
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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