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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Dibutyl carbonate
EC Number:
208-816-0
EC Name:
Dibutyl carbonate
Cas Number:
542-52-9
Molecular formula:
C9H18O3
IUPAC Name:
dibutyl carbonate

Sampling and analysis

Analytical monitoring:
yes

Test solutions

Vehicle:
no

Test organisms

Test organisms (species):
Daphnia magna

Study design

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

Test conditions

Test temperature:
room temperature over the test exposure was between 20.8 and 21.2°C.
pH:
8.0
Dissolved oxygen:
7.9 - 9.1 mg/l
Details on test conditions:
TEST SYSTEM
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
Reference substance (positive control):
yes
Remarks:
potassium dichromate

Results and discussion

Effect concentrations
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
68.5 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 54.2 - 94.4 mg/l 95% CL

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Executive summary:

Administrative data: add

- Purpose flag if key study

- "used for MSDS" if key study

- data: Study period if possible, otherwise delete entry

Data source:

- add year

- add date

- add company study number or report number if stated

- Check performing laboratory

Test material: add

- CAS #

- Name of test material (as cited in study report)

- Analytical purity, physical state?

Vehicle: yes/no?

Test conditions: check

- Test temperature

- pH

- Dissolved oxygen

- nominal and measured concentrations

- Details on test conditions

- No of vessels per concentration

- No of vessels per control

Results and discussion: add

- Effect concentrations

Any other information on results incl. tables:

- fill in table, replace ConcX with the real test concentrations