Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP guideline study without anayltical monitoring

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987
Report date:
1987

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Sulfoisophtalsäure Na-Salz sulfatarm
IUPAC Name:
Sulfoisophtalsäure Na-Salz sulfatarm
Details on test material:
- Name of test material (as cited in study report): Sulfoisophtalsäure Na-Salz sulfatarm
- Analytical purity: 85-88 %; 12-15% water
Specific details on test material used for the study:
Details on properties of test surrogate or analogue material (migrated information):
Data on the aquatic toxicity of ‘4-Sulfophthalic acid, disodium salt’ is used to fill data gaps where data are not available for the submission item. For details on the analogue/category rationale please see respective document attached to section 13 of this technical dossier.

Sampling and analysis

Analytical monitoring:
no

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:
18.9-20.8 °C
pH:
3.39-8.16
Dissolved oxygen:
7.6 - 9.3 mg/l
Nominal and measured concentrations:
Nominal test concentrations (mg/L):
Details on test conditions:
TEST SYSTEM
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
EC0
Effect conc.:
62.5 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
88.39 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 88.39-88.39 mg/l 95% CL
Duration:
48 h
Dose descriptor:
EC100
Effect conc.:
125 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mobility

Applicant's summary and conclusion