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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2020
Report date:
2020

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
yes
Remarks:
Minor deviation with no impact on study reliability
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
5-(dihydroxyboranyl)benzene-1,3-dicarboxylic acid
Cas Number:
881302-73-4
Molecular formula:
C8H7BO6
IUPAC Name:
5-(dihydroxyboranyl)benzene-1,3-dicarboxylic acid
Test material form:
solid

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
Total exposure duration:
48 h

Test conditions

Test temperature:
20°C ± 2°C
pH:
between 6.3 and 7.8
Dissolved oxygen:
between 8.0 and 8.4 mg/L
Nominal and measured concentrations:
Since the deviation between the measured concentrations and the nominal concentrations was
within the range of ± 20 %, analysis of the results were based in the nominal concentrations.
Reference substance (positive control):
yes
Remarks:
potassium dichromate

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
EC10
Effect conc.:
>= 73.6 - <= 86.5 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
24 h
Dose descriptor:
EC10
Effect conc.:
>= 73.6 - <= 86.5 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Key result
Duration:
24 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Results with reference substance (positive control):
EC50 with reference item over a period of 24 hours (No GLP results):
*Actual value: 1.65 mg/L
*Reference value: between 0.6 and 2.1 mg/L
*Compliance: yes

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The acute effects of 3,5-DICARBOXYPHENYLBORONIC ACID at the definitive nominal concentrations of 0; 11.96; 20.36; 34.6; 58.84 and 100.0 mg test item.L-1 to Daphnia magna were investigated under laboratory conditions. Validity criteria are met. Results show that EC50-48H is greater than 100 mg/L for the test item.
Executive summary:

The aim of this study was to assess the effects of the test item 3,5-DICARBOXYPHENYLBORONIC ACID on the mobility of Daphnia magna over a period of 48 hours under static conditions according to OECD Guideline 202 (April 2004). Daphnia magna is a freshwater crustacean that is recommended by the OECD Guideline 202.
The test item is a soluble product under the test conditions and the test solutions were prepared in the test medium by dilution of a primary stock solution of test item.
The acute effects of 3,5-DICARBOXYPHENYLBORONIC ACID at the definitive nominal concentrations of 0; 11.96; 20.36; 34.6; 58.84 and 100.0 mg test item.L-1 to Daphnia magna were investigated under laboratory conditions.
The analytical samples were sampled at the beginning of the test and at the end of the test in the content of the vessels pooled and homogenised.
Since the deviation between the measured concentrations and the nominal concentrations was within the range of ± 20 %, analysis of the results was based in the nominal concentrations.

EC50-24h (95% confidence limits) >100 mg/L
EC50-48h (95% confidence limits) >100 mg/L
EC10-24h (95% confidence limits) 80.0 mg/L (73.6 – 86.5)
EC10-48h (95% confidence limits) 80.0 mg/L (73.6 – 86.5)