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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 206-076-3 | CAS number: 299-29-6
- 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_ecotoxicological-information.png)
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 24 October through the 27 October, 2000
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with generally accepted scientific standards and described in sufficient detail
- Qualifier:
- according to guideline
- Guideline:
- ISO 10253 (Water quality - Marine Algal Growth Inhibition Test with Skeletonema costatum and Phaeodactylum tricornutum)
- GLP compliance:
- yes
- Details on test solutions:
- Nominal concentrations of the test material over a range of 56.2, 100.0, 177.8, 316.2, 562.3. and 1000.0 mg/L were prepared in Guillard's f/2 + Si test media from the stock solution.
- Test organisms (species):
- Skeletonema costatum
- Details on test organisms:
- Supplier: Culture Collection of Algae and Protozoa. Dunstaffnage
Stock cultures were maintained in Guillard's f/2 medium + Si in accordance with STL Runcorn SOP 1.18. - Test type:
- static
- Water media type:
- saltwater
- Total exposure duration:
- 3 d
- Remarks on exposure duration:
- Exposures were conducted between 24 October and 27 October 2000.
- Post exposure observation period:
- 2 ml sub-samples of the contents of each test vessel were removed after 24, 48 and 72 hours of incubation and cell numbers determined according to STL Runcorn SOP III.19
- Hardness:
- No data
- Test temperature:
- 20 ± 2°C
- pH:
- pH range 5.73-8.90
- Dissolved oxygen:
- Dissolved Oxygen range: 82.7-98.8 %
- Salinity:
- No data
- Nominal and measured concentrations:
- Nominal concentrations of the test material over a range of 56.2, 100.0, 177.8, 316.2, 562.3. and 1000.0 mg/L were prepared in Guillard's f/2 + Si test media from the stock solution.
- Details on test conditions:
- Six replicate control flasks and three replicate flasks at each test concentration and reference material, were prepared with algae added from a culture concentrate to give an initial algal cell concentration of approximately 8820 cells per ml. The culture flasks were incubated in a rotary incubator at a target temperature of 20 ± 2°C under constant illumination for 72 hours.
- Reference substance (positive control):
- yes
- Remarks:
- 3,5- dichlorophenol
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 265.7 mg/L
- Basis for effect:
- growth rate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 106.2 mg/L
- Basis for effect:
- growth rate
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 88.2 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 56.2 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 100 mg/L
- Basis for effect:
- growth rate
- Details on results:
- From this study the 72 hour EC50 value tor the test substance was determined to be 265.7 mg/L. The 24 and 48 hour values were determined to be 106.2 and 88.2 mg/L respectively.
The No Observed Effect Concentration, (NOEC), after 72 hours was determined to be 56.2 mg/L. The Lowest Observed Effect Concentration. (LOEC), was determined to be 100.0 mg/L.
Concentrations of 316.2, 562.3, and 1000.0 mg/L produced greater than 100% inhibition after 24 hours exposure. After 48 hours exposure concentrations of 562.3 and 1000.0 mg/L produced greater than 100% inhibition. Greater than 100% inhibition was also evident at 1000.0 mg/L after 72 hours exposure. There was evidence of a dose response in this study.
Microscopic examination indicated no unusual cell growth or deformity at any of the test concentrations. - Reported statistics and error estimates:
- The growth rate, u, was determined for each test flask using the following equation:
u= ( In Nn - In No )/ tn
tn = time of the final measurement (days) after the beginning of the test
No = the nominal, or measured, initial cell density
Nn= the measured final cell density at time. n
From the calculated growth rates the percentage inhibition, (Iui) for each test concentration was determined using the following equation:
Iui = ((Uc-Ui)/Uc) X 100
Iui = the percentage inhibition (growth rate) for test concentration i
Ui = the mean growth rate for test concentration i
Uc = the mean growth rate for the control
The concentration of test material required to cause 50% inhibition of growth rate (EC50) was determined using the statistical computer programme, Toxcalc, supplied by Tidepool Scientific. (STL Runcorn SOP V.4). - Conclusions:
- The 72 hour EC50 for expsoure to iron gluconate to the algae Skeletonema costatum is 265.7 mg/L.
Iron Gluconate is classified as non-hazardous for this end point - Executive summary:
In study, a sample of iron gluconate was assessed for its potential toxicity to the marine alga Skeletonema costatum in a static test over 72 hours according to the procedure described in ISO/DIS 10253 and as detailed in STL Runcorn SOP III. 19. Test concentrations were prepared over the range 56.2 to 1000.0 mg/L. Cultures of Skeletonema costatum were exposed to determine the concentration which inhibited algal growth rate by 50% over 72 hours (EC5o). From this study the 72 hour EC50 value was determined to be 265.7 mg/L. The 24 and 48 hour values were determined to be 106.2 and 88.2 mg/L respectively.
Iron Gluconate is classified as non-hazardous for this end point
Reference
In this study the effective concentration of the test substance which inhibited the algal growth rate by 50% after 72 hours exposure (72 hour EC50) was determined to be 265.7 mg/L. The pH readings for the test concentrations 56.2 - 1000.0 mg/L at the start of the study were below the acceptable tolerance limit of 7.80-8.20. pH for the test volumes was adjusted to within acceptable limits before the inoculum was added. It was noted that the test media changed from clear to a yellow/orange colouration upon addition of the test material. This increased with increasing concentration.
Description of key information
A sample of iron gluconate was assessed for its potential toxicity to the marine alga Skeletonema costatum in a static test over 72 hours according to the procedure described in ISO/DIS 10253 and as detailed in STL Runcorn SOP III. 19. Test concentrations were prepared over the range 56.2 to 1000.0 mg/L. Cultures of Skeletonema costatum were exposed to determine the concentration which inhibited algal growth rate by 50% over 72 hours (EC50). From this study the 72 hour EC50 value was determined to be 265.7 mg/L. The 24 and 48 hour values were determined to be 106.2 and 88.2 mg/L respectively.
Iron Gluconate is classified as non-hazardous for this end point
Key value for chemical safety assessment
- EC50 for marine water algae:
- 265.7 mg/L
- EC10 or NOEC for marine water algae:
- 56.2 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.
![ECHA](/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/echa_logo.png)