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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 942-225-5 | CAS number: -
- 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
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Dec 2002 to Jan 2003
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Deviations:
- no
- GLP compliance:
- yes
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: Schering AG, Bergkamen, Germany (61703003)
- Purity: 99.5 %
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Solubility and stability of the test substance in the solvent/vehicle: S20°c> 546 g/L (according to Schering report A09525)
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Amount of substance in test solution (nominal) : 321 mg/L
OTHER SPECIFICS:
Vapor pressure: P25 < 10·3 Pa (according to Schering report A07301)
Hydrolytical stability: t½ > 1 year at 25°C (according to Schering report A08129) - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): The activated sewage sludge for the inoculum was collected on the day before the start of the experiment from a well-operated municipal sewage treatment plant ("Klaranlage Berlin Ruhleben"), predominantly dealing with domestic sewage. Upon arrival at the laboratory, the activated sludge was stirred and aerated for approximately two hours. Thereafter, the sludge was homogenized in a blender. Then it was allowed to settle for approximately 30 minutes. 3 mL corresponding to 9 to 15 mg suspended solids were taken from the supernatant for each test vessel. The nutrient solution (mineral medium) was prepared according to the OECD guideline 301F (1).
- Duration of test (contact time):
- 29 d
- Initial conc.:
- 200 mg/L
- Based on:
- ThOD
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium: 200 mg ThOD/L:
- Test temperature: 21 to 22°C
- pH: 7.7 to 7.8
- pH adjusted: no
TEST SYSTEM
- Method used to create aerobic conditions: For the determination of the 02 consumed, an electronical manometric device, mounted on the top of each bottle was employed (WTW OxyTop C6).
- Details of trap for CO2 and volatile organics if used: The produced CO2 was absorbed by an absorbing agent (soda lime) installed inside. The resulting negative pressure was recorded by the electronical rnanometric device and calculated as mg 02/L consumption. The recorded values were transmitted to a portable controller instrument by infrared technique (WTW OxyTop OCl 10) and subsequently transferred to a laboratory computer by a serial connection cable. The percentage calculation of the degradation rate from the transferred data were performed by Microsoft Excel.
CONTROL AND BLANK SYSTEM
- Toxicity control: Iotroxic acid disodium salt +sodium acetate (100 mg + 100 mg ThOD/L) (single set)
- Blank control: 0mgThOD/L (triplicate) - Reference substance:
- acetic acid, sodium salt
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- 0
- Sampling time:
- 29 d
- Results with reference substance:
- The reference compound sodium acetate was degraded to 89 % on day 29 (28 days of incubation). 60% degradation was reached between day 2 and 6.
In the toxicity control, the reference compound (sodium acetate) plus the test compound iotroxic acid disodium salt, was degraded to 44 % on day 29 (28 days of incubation), which reflected the degradation in the individual sets. - Validity criteria fulfilled:
- yes
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The test compound iotroxic acid disodium salt was not degraded up to day 29 (28 days of incubation).
- Executive summary:
In a 28 day study on the biodegradability of iotroxic acid, disodium salt in the manometric respiration test, iotroxic acid disodium salt was incubated in an freshwater aqueous solution including nutrients with microorganisms from a municipal sewage treatment plant for 28 days (start of treatment= day 1). The biological degradation of the test and reference substances was evaluated by measurement of the 02 consumption during the test period. The test substance iotroxic acid, disodium salt was incubated at a concentration of 200 mg theoretical oxygen demand (Th OD) per litre. Additionally, a reference substance (sodium acetate) was tested in a single set according to the same procedure, in order to verify the viability and activity of the degrading microorganisms. One further set was incubated with sodium acetate at 100 mg ThOD/L (reference substance) plus iotroxic acid disodium salt at 100 mg ThOD/L representing a toxicity control. Furthermore, a blank control was tested in triplicate without any test or reference substance.
The test compound iotroxic acid disodium salt was not degraded up to day 29 (28 days of incubation). The reference compound sodium acetate was degraded to 89 % on day 29 (28 days of incubation). 60% degradation was reached between day 2 and 6.
In the toxicity control, the reference compound (sodium acetate) plus the test compound iotroxic acid disodium salt, was degraded to 44 % on day 29 (28 days of incubation), which reflected the degradation in the individual sets. In accordance with the OECD 301F (1), the test compound iotroxic acid disodium salt is not readily biodegradable under the conditions of the test and it was not toxic to the microbes of activated sludge.
Reference
Biological degradation (cumulative) in percent (corrected for blank 02 consumption) of iotroxic acid, disodium salt (ZK 232105) | |||||||||
Test compound | Conc. expressed in theoretical O2 demand | Day of sampling | |||||||
2 | 6 | 10 | 14 | 18 | 22 | 26 | 29 | ||
Iotroxic acid, disodium salt | 200 mg/L | 0.0 | 0.0(1) | 0.0(1) | 0.0(1) | 0.0(1) | 0.0 | 0.0 | 0.0 |
Reference (sodium acetate) |
200 mg/L | 17.5 | 70.7 | 84.2 | 85.5 | 86.2 | 87.5 | 88.3 | 88.5 |
Toxicity control (iotroxic acid disodium salt+ sodium acetate) |
100 mg/L + 100 mg/L | 19.5 | 39.7 | 41.8 | 43.3 | 44.0 | 44.0 | 43.8 | 44.0 |
(1) negative values are considered as 0% degradation |
Description of key information
The test compound iotroxic acid disodium salt was not degraded up to day 29 (28 days of incubation).
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
- Type of water:
- freshwater
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.