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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
Study period:
Jun.- Nov. 2011
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: study conducted under GLP conditions and in acc. with OECD guideline

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2011

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), 5'→5'-ester with 3-(aminocarbonyl)-1-β-d-ribofuranosylpyridinium hydroxide, inner salt, disodium salt
EC Number:
246-129-8
EC Name:
Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), 5'→5'-ester with 3-(aminocarbonyl)-1-β-d-ribofuranosylpyridinium hydroxide, inner salt, disodium salt
Cas Number:
24292-60-2
Molecular formula:
C21H28N7O17P3.2Na
IUPAC Name:
Adenosine 5'-(trihydrogen diphosphate), 2'-(dihydrogen phosphate), 5'→5'-ester with 3-(aminocarbonyl)-1-β-d-ribofuranosylpyridinium hydroxide, inner salt, disodium salt
Constituent 2
Reference substance name:
b-NADP, Disodium salt
IUPAC Name:
b-NADP, Disodium salt
Details on test material:
- Molecular formula (if other than submission substance): C21H26N7O17P3Na2
- Molecular weight (if other than submission substance): 787.4
- Analytical purity: 98%
- Other: White powder

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:
yes
Total exposure duration:
48 h

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
100 mg/L
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Executive summary:

Acute Toxicity Study in Daphnia magna with b-NADP, Disodium salt.

The study procedures described in this report were based on the OECD guideline No. 202, 2004. In addition, the procedures were designed to meet the test methods of theCommissionRegulation (EC) No440/2008,Part C.2, 2008 and the ISO International Standard 6341, 1996.

The batch of b-NADP, Disodium salt tested was a white powder with a purity of 98% and completely soluble in test medium at the concentrations tested.

A combined limit/range-finding test was performed. Preparation started with a concentration of 100 mg/l. No other treatment than vigorous shaking was needed to completely dissolve the test substance. The lower test concentrations were prepared by subsequent dilutions of the highest concentration in test medium. The final test solutions were all clear and colourless.

Twenty daphnids per group (5 per vessel, 4 vessels) were exposed to a control and a concentration of 100 mg/l in a limit test. In addition, ten daphnids per group (5 per vessel, 2 vessels) were exposed to 0.1, 1.0 and 10 mg/l in a range-finding test. The total exposure period was 48 hours and samples for analytical confirmation of exposure concentrations were taken at the start and at the end of the test.

The measured concentration in the sample taken from the nominal concentration of 100 mg/l was in agreement with nominal and remained stable during the test.

Based on these results, the effect parameters were expressed in terms of analytically confirmed nominal concentrations.

The study met the acceptability criteria prescribed by the protocol and was considered valid.

b-NADP, Disodium salt did not induce acute immobilisation of Daphnia magna at analytically confirmed nominal concentration of 100 mg/l after 48 hours of exposure (NOEC).

The 48h-EC50was beyond the range tested, i.e. exceeded an analytically confirmed nominal concentration of 100 mg/l.