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EC number: 483-940-8 | 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:
- key study
- Study period:
- From January 11, 2010 to March 25, 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)
- GLP compliance:
- yes
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- - Source: In-house laboratory culture
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- 24 and 48 hours.
- Nominal and measured concentrations:
- 0.1, 1.0, 10 and 100 mg/l
- Details on test conditions:
- - Test volume: 80 mL
- Aeration: None
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4 replicates for the highest test concentration and 2 replicates for other test concentration
- No. of vessels per control (replicates): 4
- Photoperiod: 16-hr photoperiod daily - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- The 48h-EC50 was 0.38 mg/l.
- Validity criteria fulfilled:
- yes
- Conclusions:
- According to OECD 202 test method, the 48-hr EC50 of Everzol Red CDN Crude was >100 mg/L.
- Executive summary:
This test using the procedures outlined in the NOTOX Study Plan for 492366 and OECD 202 (OECD, 2004). The results of this OECD 202 test for Everzol Red CDN Crude show that all validity criteria were met. Under the conditions of this test, the 48-hr EC50 of Everzol Red CDN Crude was >100 mg/L.
Reference
Table 1. Acute immobilization of daphnids after 24 and 48 hours
Concentration Everzol Red CDN Crude (mg/l) |
Vessel number |
Number Daphnia exposed |
Response at 24 h |
Response at 48 h |
||
number |
Total % |
number |
Total % |
|||
control |
A |
5 |
0 (4) |
0 |
0 (3) |
10 |
B |
5 |
0 (1) |
0 (1) |
|||
C |
5 |
0 (5) |
1 (2) |
|||
D |
5 |
0 (4) |
1 (5) |
|||
0.10 |
A |
5 |
0 (5) |
0 |
0 (3) |
0 |
B |
5 |
0 (2) |
0 (3) |
|||
1.0 |
A |
5 |
0 (1) |
0 |
0 (1) |
0 |
B |
5 |
0 (2) |
0 |
|||
10 |
A |
5 |
0 (3) |
0 |
0 (2) |
0 |
B |
5 |
0 (3) |
0 (1) |
|||
100 |
A |
5 |
0 |
0 |
0 |
0 |
B |
5 |
0 |
0 |
|||
C |
5 |
0 |
0 |
|||
D |
5 |
0 |
0 |
Between brackets: number of daphnids trapped at the surface. There daphnids were reimmersed into the respective solution before recording of immobility.
Table 2. Effect parameters
Parameter |
Concentration Everzol Red CDN Crude (mg/l) |
NOEC |
100 |
24 & 48h-EC50 |
>100 |
Table 3. pH and oxygen concentrations
ConcentrationEverzol Red CDN Crude(mg/l) |
Start (t=0 h) |
t=24 h old |
t=24 h fresh |
End (t=48 h) |
||||
pH |
O2 |
pH |
O2 |
pH |
O2 |
pH |
O2 |
|
control |
7.6 |
9.2 |
7.4 |
8.8 |
7.4 |
9.0 |
7.7 |
8.9 |
100 |
7.6 |
9.2 |
7.7 |
8.7 |
7.4 |
9.0 |
7.5 |
8.9 |
Description of key information
The 48-hr EC50 of Everzol Red CDN Crude was >100 mg/L for Daphnia magna (OECD TG202).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 100 mg/L
Additional information
Not more than 10 % of the Daphnia were immobilised in the control and the dissolved oxygen concentration at the end of the test was ≥3 mg O2/L. All test validity criteria were met. The pH of the test solutions was within the ranges outlined in the OECD 202 test guideline for limit test. Under the conditions of this test, the 48h-EC50of Everzol Red CDN Crude was greater than 100.00 mg/L.
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