Acute toxicity - Category 4, Oral
Acute toxicity - Category 4, Dermal
Acute toxicity - Category 4, Inhalation
Hazardous to the aquatic environment, short-term (Acute) - Category Acute 1
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 1
H302 Harmful if swallowed
H312 Harmful in contact with skin
H332 Harmful if inhaled
H400 Very toxic to aquatic life
H410 Very toxic to aquatic life with long lasting effects
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P273 Avoid release to the environment.
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P317 Get medical help.
P321 Specific treatment (see ... on this label).
P362+P364 Take off contaminated clothing and wash it before reuse.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P391 Collect spillage.
none
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest. Refer for medical attention.
Remove contaminated clothes. Rinse and then wash skin with water and soap.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Refer for medical attention .
Inhalation or ingestion causes headache, drowsiness, nausea, and blue color in lips, ears, and fingernails (cyanosis). Contact with eyes causes irritation. Can be absorbed through the intact skin to give same symptoms as for inhalation. (USCG, 1999)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Dinitrophenol and Related Compounds
If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use foam, dry chemical, or carbon dioxide. Keep run-off water out of sewers and water sources. Nitrophenols
Special Hazards of Combustion Products: Toxic and irritating fumes of unburned material and oxides of nitrogen can form in fire. (USCG, 1999)
Use dry powder, carbon dioxide, water spray, alcohol-resistant foam.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers.
Collect and arrange disposal. Keep the chemical in suitable and closed containers for disposal. Remove all sources of ignition. Use spark-proof tools and explosion-proof equipment. Adhered or collected material should be promptly disposed of, in accordance with appropriate laws and regulations.
NO open flames. Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Store in an area without drain or sewer access. Separated from strong oxidants, strong bases, strong acids and food and feedstuffs.
no data available
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear safety goggles.
Protective gloves.
Use local exhaust or breathing protection.
no data available
Solid. Needles or prismas.
Yellowish.
Peculiar, aromatic color
44 °C. Atm. press.:1 013 hPa.
214 °C. Atm. press.:1 013 hPa.
Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
no data available
100.5 °C. Atm. press.:1 013 hPa.
485 °C. Atm. press.:1 013 hPa. Remarks:Temperature class: T1.
no data available
no data available
no data available
Miscible with water
log Pow = 1.77.
0.069 hPa. Temperature:20 °C.;0.2 hPa. Temperature:30 °C.;1 hPa. Temperature:50 °C.
1.495 g/cm3. Temperature:20 °C.
(air = 1): 4.81
no data available
Decomposes on burning. This produces toxic and corrosive fumes including nitrogen oxides. Reacts with strong acids, strong bases and strong oxidants.
May explode on heating. On combustion, forms nitrogen oxides. Decomposes on heating. This produces toxic fumes including nitrogen oxides. Reacts with strong oxidants.
no data available
AROMATIC NITROCOMPOUNDS ARE FLAMMABLE ... /AROMATIC NITROCMPD/Dust explosion possible if in powder or granular form, mixed with air.2-NITROPHENOL is a yellow, crystalline material, moderately toxic, low melting point (45° C). When heated to decomposition it emits toxic fumes of oxides of nitrogen. In molten form violent reaction with strong alkali (85% potassium hydroxide) [491 M, 1975, p. 342]. Reaction product with chlorosulfuric acid decomposes violently at room temperature [Vervalin, C. H., Hydrocarbon Proc., 1976, 55(9), p. 321].
no data available
The molten ortho-nitrophenol reacts violently with commercial 85% potassium hydroxide pellets. (possibly involving formation of the aci-o-nitroquinonoid salt).
When heated to decomp it emits toxic fumes of /nitrogen oxides/.
no data available
no data available
no data available
no data available
no data available
no data available
The substance is mildly irritating to the eyes and skin. Ingestion could cause effects on the blood. This may result in the formation of methaemoglobin.
no data available
A harmful concentration of airborne particles can be reached quickly.
AEROBIC: More than 64 days were required to biodegrade 2-nitrophenol in an aqueous soil solution(1) however 2-nitrophenol was completely degraded in 7-14 days in a second soil inoculum(2). 2-Nitrophenol was mineralized 10% in a terrestrial ecosystem over the course of 10 days(3). 2-Nitrophenol, present at 100 mg/L, reached 0% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(4). A half-life of about 37 days was observed for 2-nitrophenol in a laboratory batch microcosm incubated with sediment and groundwater(5). 2-Nitrophenol was degraded over 80% in an aerobic groundwater/sediment microcosm from a landfill during a 60 day incubation period(6). First-order rate constants of 0.01/day to 0.05/day were determined for 2-nitrophenol in aerobic aquifer material(7), corresponding to half-lives of about 14-69 days(SRC).
BCF values of <2.2 to 5 were measured for carp (Cyprinus carpio) exposed to 1 ppm of 2-nitrophenol over a 6 week incubation period(1); BCF values of <22 were measured for carp exposed to 0.1 ppm 2-nitrophenol over a 6 week incubation period(1). According to a classification scheme(2), these BCF values suggest bioconcentration in aquatic organisms is low.
The Koc of 2-nitrophenol in five reference European soils (pH 3.2-7.4) ranged from 32.1 to 265.7 with Koc generally decreasing with increasing pH(1); similar Koc values were determined for a second-generation set of five reference European soils(2). The Koc for 2-nitrophenol in Brookston clay loam was 114(3). In sorption studies using peat, 2-nitrophenol had measured Koc values of 85 (when 2-nitrophenol was in the neutral state) and 13 (when 2-nitrophenol existed as anionic species)(4). According to a classification scheme(5), a Koc range of 13 to 265 suggests that 2-nitrophenol is expected to have very high to moderate mobility in soil. The pKa of 2-nitropehnol is 7.23(6), indicating that this compound will exist partially in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(7).
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: UN1663 (For reference only, please check.)
IMDG: UN1663 (For reference only, please check.)
IATA: UN1663 (For reference only, please check.)
ADR/RID: NITROPHENOLS (o-, m-, p-) (For reference only, please check.)
IMDG: NITROPHENOLS (o-, m-, p-) (For reference only, please check.)
IATA: NITROPHENOLS (o-, m-, p-) (For reference only, please check.)
ADR/RID: 6.1 (For reference only, please check.)
IMDG: 6.1 (For reference only, please check.)
IATA: 6.1 (For reference only, please check.)
ADR/RID: III (For reference only, please check.)
IMDG: III (For reference only, please check.)
IATA: III (For reference only, please check.)
ADR/RID: Yes
IMDG: Yes
IATA: Yes
no data available
no data available
Specific treatment is necessary in case of poisoning with this substance; the appropriate means with instructions must be available.