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Diss Factsheets

Ecotoxicological information

Short-term toxicity to aquatic invertebrates

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Administrative data

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Aug - Sep 1990
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1990
Report date:
1990

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Version / remarks:
1984
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
Version / remarks:
1984
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7-bis(diethylamino)phenoxazin-5-ium acetate
EC Number:
279-349-8
EC Name:
3,7-bis(diethylamino)phenoxazin-5-ium acetate
Cas Number:
79916-07-7
Molecular formula:
C20H26N3O.C2H3O2
IUPAC Name:
3,7-bis(diethylamino)phenoxazin-5-ium acetate
Test material form:
solid: particulate/powder

Sampling and analysis

Analytical monitoring:
yes
Details on sampling:
Analytical measurements of the test article were performed in the stock solution and the test media of the nominal test concentrations 0.0625, 0.25 and 1 mg test article/L at the start and the end of the test by sampling freshly prepared test media and media, which were incubated under the same conditions as in the test itself during test duration.

The samples were stored deep-frozen (-20°C) until the analysis was performed.

Test solutions

Vehicle:
no
Details on test solutions:
A stock solution was prepared by dissolving the test article in test water (1 g/L). The stock solution was diluted in a series of sequential dilutions with test water and adequate volumes of these stock solutions were added to obtain the following nominal test concentrations: 0.0625, 0.125, 0.25, 0.50 and 1.0 mg/L and a control (test water without any additions).

Test organisms

Test organisms (species):
Daphnia magna
Details on test organisms:
The study was performed with young Daphnia magna (6-24 h old), bred in the laboratories of RCC under standardized conditions. The parental Daphnia were maintained in the same reconstituted water as in the test for at least 24 h prior to the start of the test.

Study design

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

Test conditions

Hardness:
2.5 mmol/L CaCO3
Test temperature:
20.5 - 20.6°C
pH:
7.9 - 8.0
Dissolved oxygen:
9.0 - 9.2 mg/L
Nominal and measured concentrations:
Nominal: 0 (control), 0.0625, 0.125, 0.250, 0.500, 1.00 mg/L
Measured (geometric mean): 0 (control), 0.0679 (109%), 0.236 (94%), 0.955 (96%)
Details on test conditions:
TEST SYSTEM
- Test vessel: glass beaker
- Material, size, headspace, fill volume: 100 mL total volume, 50 mL fill volume
- Aeration: no
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4

TEST MEDIUM / WATER PARAMETERS
- Alkalinity: 0.8 mmol/L
- Ca/mg ratio: 4:1
- Culture medium different from test medium: no

OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 16 light / 8 darkness
- Light intensity: 200 - 600 lux

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : mobility at 24 and 48 h
Reference substance (positive control):
not specified

Results and discussion

Effect concentrations
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
0.239 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 95% CI: 0.203 - 0.280 mg/L
Details on results:
0% immbolity in control
Analytical verification of test item within 80 - 120% recovery range
Reported statistics and error estimates:
Probit analysis

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The test item was found to be acutely toxic to Daphnia magna. The 48-h EC50 was determined at 0.239 mg/L (nominal, analytically verified.)