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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1996-11-18 - 1996-11-22
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Guideline study without deviations. non-GLP

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 203 (Fish, Acute Toxicity Test)
Deviations:
no
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Poly(oxy-1,2-ethanediyl), a,a',a'',a'''-[1,2-ethanediylbis(nitrilodi-2,1-ethanediyl)]tetrakis[w-hydroxy-
EC Number:
608-035-9
Cas Number:
27014-42-2
IUPAC Name:
Poly(oxy-1,2-ethanediyl), a,a',a'',a'''-[1,2-ethanediylbis(nitrilodi-2,1-ethanediyl)]tetrakis[w-hydroxy-

Sampling and analysis

Analytical monitoring:
yes

Test organisms

Test organisms (species):
Danio rerio (previous name: Brachydanio rerio)
Details on test organisms:
Breeding by HOECHST AG, Hoechst Marion Roussel, Drug Safety
The fish had a mean body length of 3.1 cm (2.7 - 3.3 cm/ s = ± 0.22)

Study design

Test type:
not specified
Water media type:
freshwater
Limit test:
no
Total exposure duration:
96 h

Test conditions

Test temperature:
21.3 - 21.5 (°C)
pH:
7.6-8.1
Dissolved oxygen:
6.3-10.0 mg/l

Results and discussion

Effect concentrations
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 10 000 mg/L
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Details on results:
The fish of 10,000 mg / L group showed symptoms during the entire experimental period but showed no lethality.
In the control group (0 mg/l) also no lethality appeared.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The LC 50 after 96 hours is >10000 mg / L.
Executive summary:

The LC 50 after 96 hours is >10000 mg / L.