Registration Dossier
Registration Dossier
Diss Factsheets
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EC number: 939-338-7 | 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

Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
Description of key information
Data waiving: Based on the ready biodegradability study the test substance is not toxic to microorganisms.
Absence of microbial toxicity can be inferred from biodegradation studies in the laboratory. The information content of ready biodegradability tests can be used to derive a NOEC. The assumption that the substance under investigation is not inhibitory to the micro-organisms when dosed in the test system is implicit in ready biodegradability testing. If a compound does not inhibit the degradation of a positive control at a certain concentration, this concentration can be used as a NOEC value.
Any Ready Biodegradability Test relying on continuous monitoring or the Manometric Respirometry test (OECD 301F) is considered more reliable for observing the effects of a chemical on the inoculum.
Based on the ready biodegradability study the test substance is not toxic to microorganisms since it does not inhibit the degradation of a positive control at 100 mg/L. Therefore, this concentration can be used as a NOEC value.
Key value for chemical safety assessment
- EC10 or NOEC for microorganisms:
- 100 mg/L
Additional information
Data waiving: Based on the ready biodegradability study the test substance is not toxic to microorganisms.
Absence of microbial toxicity can be inferred from biodegradation studies in the laboratory. The information content of ready biodegradability tests can be used to derive a NOEC. The assumption that the substance under investigation is not inhibitory to the micro-organisms when dosed in the test system is implicit in ready biodegradability testing. If a compound does not inhibit the degradation of a positive control at a certain concentration, this concentration can be used as a NOEC value.
Any Ready Biodegradability Test relying on continuous monitoring or the Manometric Respirometry test (OECD 301F) is considered more reliable for observing the effects of a chemical on the inoculum.
Based on the ready biodegradability study the test substance is not toxic to microorganisms since it does not inhibit the degradation of a positive control at 100 mg/L. Therefore, this concentration can be used as a NOEC value.
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.

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