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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Ecotoxicological information

Short-term toxicity to aquatic invertebrates

Administrative data

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
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 202 (Daphnia sp. Acute Immobilisation Test)
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
Yellow MGi 1301
IUPAC Name:
Yellow MGi 1301
Test material form:
solid

Sampling and analysis

Analytical monitoring:
yes

Test organisms

Test organisms (species):
Daphnia magna

Study design

Test type:
semi-static
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
48 h

Test conditions

Nominal and measured concentrations:
200 mg/l (nominal)
Details on test conditions:
A limit test was performed to demonstrate that the test substance has no toxic effect on the test animals up to the concentration of nominal 200 mg test substance/I. Thus the only concentration tested was nominal 200 mg test substance/l and a control.
The analytically determined test substance concentrations in the freshly prepared test media varied between 101 and 102 % of the nominal value. During the renewal period of 24 hours a decrease of test substance concentration to 54 % of the nominal value was measured, if the quantification is based on the main compound. If the quantification is based on the sum of main compound and main degradation product 104 % of the nominal value were found.
Since the analytically determined test substance concentrations at the start of the test were in good agreement with the nominal test concentration, the reported biological results are related to the nominal test substance concentration.

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
200 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 200 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility

Applicant's summary and conclusion

Conclusions:
NOEC = 200 mg/l
EC50 (48 h) > 200 mg/l