Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 202-774-7 | CAS number: 99-63-8
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of 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:
- guideline study with acceptable restrictions
- Remarks:
- This study is used for read-across and therefore has been assigned a reliability of 2 (reliable with restrictions). The study, if used in support of isophthalic acid, has a reliability of 1 (reliable without restriction).
- Justification for type of information:
- The test substance rapidly hydrolyses to isophthalic acid (IPA). Therefore, the study with IPA is being used to fulfil this data requirement. Additional documentation, provided within the IUCLID Assessment Reports section, supports the read-across approach.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Samples were collected from the test solutions containing 0, 80, 350 and 1000 mg/L of the test substance at 0 hours and 48 hours.
- Sampling method: High Performance Thin-Layer Chromatography
- Sample storage conditions before analysis: less than 20ºC - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION: The stock solution was prepared once before starting the test. The amount of test material used was 4999.8 mg. The test material was added to 5 L reconstituted water, it was allowed to dissolve after addition of NaOH for pH adjustment. The formation of a clear solution was enhanced by using a stirrer and lasted approximately 24 h. The concentration of the stock solution was 1000 mg/L. The stock solution was diluted with water to prepare the individual test concentrations.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM:
- Strain: Daphnia magna (Straus)
- Age at study initiation: 6-20 hours
- Feeding during test: None
ACCLIMATION
- Acclimation period: 6-20 hours - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 213 - 249.0 mg/L CaCO3
- Test temperature:
- 22.1 - 22.3 °C
- pH:
- 7.7 - 7.9
- Dissolved oxygen:
- 8.1 - 9.0 mg/L
- Salinity:
- freshwater
- Nominal and measured concentrations:
- Nominal Concentrations used in test: 0, 80, 130, 220, 350, 600 and 1000 mg/L
Measured Concentrations at 0 hours: 0, 74, 317, 1050 mg/L and 0, 74.3, 364, 1005 mg/L
Measured Concentrations at 48 hours: 0, 64, 303, 832 mg/L and 0, 70, 269, 920 mg/L - Details on test conditions:
- TEST SYSTEM
- Test vessel: 300 mL; height: 5 cm; diameter: 9 cm; glass
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Conductivity: at time 0 hours
0 mg/L - 580 µS/cm
80 mg/L - 600 µS/cm
130 mg/L - 760 µS/cm
220 mg/L - 850 µS/cm
350 mg/L - 970 µS/cm
600 mg/L - 1100 µS/cm
1000 mg/L - 1300 µS/cm
OTHER TEST CONDITIONS
- Adjustment of pH: initially adjusted to 7.8
- Photoperiod: light/dark (16/8 h).
- Light intensity: 940 ±. 270 Lux, which corresponds to 15.6 ± 3.4 µE x sec e-1 x m e-2
TEST CONCENTRATIONS
- Range finding study: 1, 3, 10, 30 and 100 mg/L - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 952 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 952 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Behavioural abnormalities: none
- Other biological observations: none
- Mortality of control: none - Reported statistics and error estimates:
- Probit analysis was used to determine the EC values. When less than 3 test substance concentrations caused immobilisation between 0 % and 100 % the geometrical: mean was used to determine the EC50.
- Validity criteria fulfilled:
- yes
- Conclusions:
- 48-hour EC50 could not be determined as it was greater than the highest measured concentration tested (>952 mg/L).
- Executive summary:
In accordance with GLP regulations the acute toxicity to Daphnia magna (Straus), water-flea, was investigated in a static test system during a test period of 48 hours. The study was performed according to the OECD Guideline 202, Part I, 1984. The nominal concentrations to which the test organisms were exposed were 80, 130, 220, 350, 600 and 1000 mg/L.
The analytically determined actual concentrations of the test material at the beginning of the study were found to be within the range of 91% and 105% with an average of 97.8%. After 48 hours of exposure, analysed concentrations of the test material were relatively unchanged from measurements at 0 hours. They were found to be within the range of 77% and 92% of the nominal values with an average of 84.5%.
The EC50(48 h) was >952 mg/L test substance (as sodium terephthalate), based on the mean measured exposure concentration at the highest treatment. Based on the absence of treatment-related immobilisation exceeding that observed in the salinity control, the NOEC was 952 mg TS/L.
It is thought that Isopthalic Acid was hydrolysed under test conditions. As a result it is believed that under test conditions and after pH adjustment to the required physiological value Isophthalic Acid and Isophthalic Sodium Salt were the test materials investigated in this study.
Reference
It is thought that Isopthalic Acid was hydrolysed under test conditions. As a result it is believed that under test conditions and after pH adjustment to the required physiological value Isophthalic Acid and Isophthalic Sodium Salt, respectively, were the test materials investigated in this study.
Immobilisation (%)
Nominal Concentration (mg/L) |
||||||||
Time (h) |
Control |
Salinity Control* |
80 |
130 |
220 |
350 |
600 |
1000 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
24 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
48 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
* The salinity control consisted of test medium amended with NaOH solution only.
Measured Concentrations
Nominal IPA Conc. (mg/L) |
Measured mg IPA/L, Time 0 |
% of nominal |
Measured mg IPA/L, Time 48 h |
% of nominal |
80 |
74.4 |
93 |
64 |
80 |
|
74.3 |
93 |
70 |
88 |
350 |
317 |
91 |
303 |
87 |
|
364 |
104 |
269 |
77 |
1000 |
1050 |
105 |
832 |
83 |
|
1005 |
101 |
920 |
92 |
In the report, the endpoint is given as >876 mg/L, apparently the mean measured value at the highest concentration, but based on the 48-h data only, i.e. (832 + 920)/2. This is incorrect; the mean should include the 0-h data as well, i.e. (1050 + 1005 + 832 + 920)/4 = 952 mg/L.
Description of key information
The study was conducted using isophthalic acid, the primary degradate of isophthaloyl dichloride, according to OECD 202 under GLP. Daphnia magna were exposed in a static test system over a period of 48 hours to the test substance after conversion to its sodium salt. The nominal concentrations to which the test organisms were exposed were 80, 130, 220, 350, 600 and 1000 mg/L. Exposure concentrations were verified analytically at the start and end of the test and were between 77% and 105% of the nominal values. The static 48-h EC50of the test substance (converted to its sodium salt prior to exposure) to Daphnia magna was >952 mg/L, based on the mean measured concentration at the maximum treatment applied. Based on the absence of treatment-related immobilisation exceeding that observed in the control, the NOEC was 952 mg/L.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 952 mg/L
Additional information
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.