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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 200-087-7 | CAS number: 51-28-5
- 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 soil microorganisms
Administrative data
Link to relevant study record(s)
Description of key information
Data have beenn obtained fron secondary source that include several pubblications.
PERIPLASMIC NITRATE REDUCTASE ACTIVITY FOR 2,4-DINITROPHENOL
Periplasmic nitrate reductase (NAP) activity was expressed relative to the amount of nitrite formed.
Median inhibitory concentration IC50 (mg/l) nitrate reductase activity: 45 .62 (R2 0.999).
PERIPLASMIC NITRATE REDUCTASE ACTIVITY FOR 2,4-DINITROPHENOL
The amount of formazan produced was determined by reference to a standard dose-response curve. Dehydrogenase activity (DHA) was expressed as milligrams of TPF formed per mg dry weight of cell biomass per hour.
Median inhibitory concentration IC50 (mg/l) nitrate reductase activity: > 200 (2,4-Dinitrophenol was stimulatory to dehydrogenase activity all concentrations studied).
Other observations during biodegradation in soil and sediment tests with observation of the toxicity lever for microorganisms defined that above the level of c.a 100 mg/L, 2,4 -dinitrophenol may be toxic to the degrader microorganisms (Bartha et al. 1967; Namkoong et al. 1988; Schmidt and Gier 1989).
Key value for chemical safety assessment
Additional information
2,4-Dinitrophenol showed decreasing progressive stimulation of dehydrogenase enzyme with increasing concentration (40 – 200 mg/l) while 2-nitrophenol, 4-nitrophenol and 4-bromophenol showed increasing progressive inhibition of both enzyme activities. The IC50 of the phenolic compounds to the periplasmic nitrate reductase activity were comparable (33.46 – 44.75 mg/l) but lower than those for the dehydrogenase activity (>200 mg/l). This suggested greater sensitivity of periplasmic nitrate reductase than dehydrogenase enzyme to the phenolic compounds (
J. C. Okolo*, C. O. Nweke, R. N. Nwabueze, C. U. Dike and C. E. NwanyanwuToxicity of phenolic compounds to oxidoreductases of Acinetobacter species isolated from a tropical soil, Department of Microbiology, Federal University of Technology, P. M. B.1526, Owerri, Nigeria. Scientific Research and Essay Vol. 2 (7), pp. 244-250, July 2007).
Other observations during biodegradation in soil and sediment tests with observation of the toxicity lever for microorganisms defined that above the level of c.a 100 mg/L, 2,4 -dinitrophenol may be toxic to the degrader microorganisms (Bartha et al. 1967; Namkoong et al. 1988; Schmidt and Gier 1989).
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.