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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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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:
other: see 'Remark'
Remarks:
The information of this endpoint has been provided by ECHA as a result of an inquiry, thus the full access to data in the report is not accessible to the registrant. However the reliability is estimated to be at level 1: Study conducted in accordance with generally accepted scientific principles. Possible deficiencies do not affect the quality of relevant results.

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: 92/69/EEC, C2
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
413-110-2
EC Name:
-
Cas Number:
135861-56-2
Molecular formula:
C24H30O6
IUPAC Name:
1-[2,6-bis(3,4-dimethylphenyl)-hexahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder

Sampling and analysis

Analytical monitoring:
yes

Test solutions

Details on test solutions:
Identity and concentration of auxiliary solvent for dispersal: dimethylformamide

Test organisms

Test organisms (species):
other: aquatic crustacea: DM

Test conditions

Hardness:
CA 270 mg CaCO3/L

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
EC50
Effect conc.:
> 0.1 mg/L
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 0.1 mg/L
Duration:
48 h
Dose descriptor:
EC100
Effect conc.:
> 0.1 mg/L
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
>= 0.1 mg/L
Details on results:
%Concentration loss over test: 0 ...

Applicant's summary and conclusion

Validity criteria fulfilled:
not specified
Conclusions:
Test details are not available. The 24 and 48 h EC50 values and 48 h EC 100 values of the test substance on Daphnia magna were > 0.1 mg/L nominal, the highest attainable test consentration using dimethylformamide as an auxiliary solvent. The test method was an EU C.2 limit test under GLP.
The 48 h NOEC >= 0.1 mg/L nominal.
Executive summary:

The 48 h EC50value of the test substance on Daphnia magna was > 0.1 mg/L nominal, the highest attainable test consentration using dimethylformamide as an auxiliary solvent. The test method was an EU C.2 limit test under GLP.

The 48 h NOEC >= 0.1 mg/L nominal, the solubility limit of the substance, indicating no acute toxicity at levels up to water solubility.

Concentrations were confirmed analytically.

As the study was conducted under GLP and the study was already assessed by authorities, it was considered valid, and selected as key.