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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicity to soil macroorganisms except arthropods

Administrative data

Endpoint:
toxicity to soil macroorganisms except arthropods: short-term
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study performed according to OECD 207 under China GLP regulation.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2014
Report date:
2014

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 207 (Earthworm, Acute Toxicity Tests)
Deviations:
no
GLP compliance:
yes
Remarks:
China GLP regulation

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
liquid: viscous
Details on test material:
Chemical name: 2-(4-Hydroxy-3,5-dimethoxy-benzylidene)-malonic acid bis-(2-ethyl-hexyl) ester
CAS No.: 444811-29-4

Sampling and analysis

Analytical monitoring:
no

Test substrate

Vehicle:
no
Details on preparation and application of test substrate:
The test item was directly added into the soil. A total amount of 10 g mixture of the test item and dry soil was prepared (premix). Then the premix was added to 540 g soil (dry weight) for each test container. The medium was throughly mixed and deionised water was added to give an overall moisture content of about 35 %.

Test organisms

Test organisms (species):
Eisenia fetida
Animal group:
annelids
Details on test organisms:
The test organisms were obtained from a eartworm farm in Nanjing, China

Study design

Study type:
laboratory study
Substrate type:
artificial soil
Limit test:
yes
Total exposure duration:
14 d

Test conditions

Test temperature:
20 - 22°C
pH:
6.2 - 6.5
Moisture:
30 - 36 %
Nominal and measured concentrations:
1000 mg/kg (dry weight of soil)
Reference substance (positive control):
yes
Remarks:
2-chloracetamide

Results and discussion

Effect concentrationsopen allclose all
Duration:
14 d
Dose descriptor:
LC50
Effect conc.:
> 1 000 mg/kg soil ww
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Duration:
14 d
Dose descriptor:
NOEC
Effect conc.:
1 000 mg/kg soil ww
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
behaviour
Details on results:
No mortality were observed in worms exposed to the test item at a limit concentration of 1000 mg/kg soil ww during the 14-day exposure period.
Results with reference substance (positive control):
The LC50 0f 2-chloroacetamide to Eisenia fetida was 25.1 mg/kg (dry soil) after 14 days of exposure.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The test item did not induce any toxicity to earthworms exposed to the limit concentration of 1000 mg/kg soil over a period of 14 days.
Executive summary:

The acute toxicity of the substance to adult earth worm (Eisenia fetida) was investigated in an artificial soil test according to OECD No. 207. Artificial soil was used as the test medium. The moisture content of the test medium during the course of the study was between 30 and 36% and the pH was between 6.2 and 6.5. The earth worms were exposed to a limit dose of 1000 mg/kg dry weight soil for a period of 14 days at defined temperature (20 - 22°C), humidity (80 to 85%) and under continuous light (400 to 800 lux). Each group (control and treatment group) consisted of 4 replicates with 10 worms each. No lethality was observed during the 14 -day observation period neither in the control nor in the limit treatment group. Based on the results of this study, the LC50 of the test substance exceeded 1000 mg/kg dry soil. This concentration can be considered as the NOEC as no adverse effects have been observed in the treatment group.