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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

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

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Reference substance name:
Indate (2-), hexachlorododeca-µ-methoxy-µ6-oxohexa-, hydrogen, compd. with N-methylmethanamine (1:2:2)
Cas Number:
1381802-10-3
Molecular formula:
[In6O(OMe)12Cl6]2–[NH2Me2]+2 · 2MeOH
IUPAC Name:
Indate (2-), hexachlorododeca-µ-methoxy-µ6-oxohexa-, hydrogen, compd. with N-methylmethanamine (1:2:2)
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
Batch number V107 – V110
Purity > 99 %
Molecular weight 1446.302 g/mol
Appearance Colorless, crystalline powder
Water solubility Reacts (sensitive to hydrolysis, t ½ (pH 7): approx. 5 minutes

Sampling and analysis

Analytical monitoring:
yes
Details on sampling:
The tested limit concentration of 100 mg/L of the test item iXsenic S Gen 3.4 and the control were analytically verified at the start of the exposure (0 h) and at the end of the exposure (48 h).

Test solutions

Vehicle:
no
Details on test solutions:
A stock solution (100 mg/L of the test item were weighed out) was freshly prepared with dilution water.
The test item dispersion was stirred with a magnetic stirrer (approx. 1100 rpm) at room temperature for 2 h. Since the test item is known to hydrolyse quickly (t1/2 pH 7: approx. 5 min), the reaction products were tested.

Test organisms

Test organisms (species):
Daphnia magna
Details on test organisms:
Daphnia magna STRAUS (Clone 5) was used as test organisms.
20 daphnids, divided into 4 replicates, each with 5 daphnids per limit concentration and control were tested. 2 to 24 h old daphnids were used for the study. They were obtained by removing the parental daphnids twice within 22 h. Daphnids were left for acclimatisaion for at least 2 h in dilution water.

Study design

Test type:
static
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
48 h

Test conditions

Test temperature:
During the test the incubator temperature was 19 – 20 °C.
pH:
Nominal
test item
concentration pH-value
[mg/L] 0h 48h (replicate 1-4)
100 7.10 7.69 7.63 7.60 7.56
Control 7.75 7.57 7.69 7.71 7.70
Dissolved oxygen:
Nominal
test item
concentration Dissolved O2-concentration [mg/L]
[mg/L] 0h 48h (replicate 1-4)
100 7.90 8.49 8.46 8.49 8.51
Control 8.17 7.91 8.19 8.16 8.23
Nominal and measured concentrations:
Measured TOC Concentrations in the Definitive Test

Sampling date 2013-06-05 2013-06-07
Start of the exposure, 0 End of the exposure, 48 h
Start of analysis 2013-06-05 2013-06-07
Nominal
test item
concentration
[mg/L] Total Organic Carbon (TOC)*
Measured concentration#[mg/L] Measured concentration# [mg/L] %
100 15.2 16.2 107
Control < 2.00 < 2.00 —
Reference substance (positive control):
yes
Remarks:
potassium dichromate

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Results with reference substance (positive control):
EC50: 1.66 mg/L (CI 1.48 - 2.01 mg/L)

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
At the limit concentration of 100 mg/L of the test item, no effects were observed on Daphnia magna.
Executive summary:

In the acute immobilisation test with Daphnia magna (STRAUS), the effects of the limit concentration of 100 mg/L of the test item were determined according to OECD 202 (2004) and Council Regulation (EC) No. 440/2008 Method C.2 (2008). The limit test was conducted under static conditions over a period of 48 hours.