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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2013

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:
3-(ethenyloxy)propan-1-amine
EC Number:
633-172-6
Cas Number:
66415-55-2
Molecular formula:
C5 H11 N O
IUPAC Name:
3-(ethenyloxy)propan-1-amine
Details on test material:
- Identification: Aminopropyl Vinyl Ether
- Chemical name: 3-(ethenyloxy)propan-1-amine
- Physical form: liquid
- Appearance: colourless, clear
- Water solubility: miscible
- Density: 0.891 g/cm3 (20°C)
- Purity: 99.6 corrected area-%
- Homogeneity: homogeneous
- Storage conditions: The test substance was stored at ambient temperature (avoid temperature 25°C)

Sampling and analysis

Analytical monitoring:
yes
Details on sampling:
At the start of the exposure (0 h) samples from vessels without daphnids and at the end of the exposure (48 h) samples from vessels with daphnids were analyzed. The samples were transported to the Analytical Laboratory on the day of sampling.

Test solutions

Details on test solutions:
The volume of the test substance required for preparation of the nominal concentration was calculated from the density (d=0.891 g/cm3). Prior to use, the test substance container was shaken to ensure homogeneity.The stock solution (100 mg/L) was prepared by directly pipetting 224µL of test substance to 2L of test medium and stirring for approximately 10 min (magnetic stir plate) until visibly dissolved. The lower test concentrations were prepared by dilution of this stock solution. Before the dilution is performed, the stock solution was checked for complete dissolution of the test substance. The stock solution appeared colourless-clear.
- Test groups: 0 (control), 4.6, 10, 22, 46 and 100 mg/L as nominal concentrations based on test substance mass without a correction for purity.

Test organisms

Test organisms (species):
Daphnia magna
Details on test organisms:
Daphnia magna STRAUS

Study design

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

Test conditions

Hardness:
2.20-3.20 mmol/L
Test temperature:
19.6-20.1°C
pH:
7.5-8.5
Dissolved oxygen:
8.6-8.8 mg/L
Details on test conditions:
- Replicates: 4 replicates with test animals (5 animals per replicate)
- Test vessels: glass beakers (nominal volume 100mL)
- Test volume: 50 mL
- Biological loading: 5 animals/test vessel (0.1 animals/mL)
- Aeration: none
- Diet: No feeding during the exposure time.
Reference substance (positive control):
yes
Remarks:
Sodium chloride

Results and discussion

Effect concentrations
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility

Applicant's summary and conclusion

Validity criteria fulfilled:
yes