Acute toxicity - Category 3, Oral
Acute toxicity - Category 3, Dermal
Acute toxicity - Category 3, Inhalation
Specific target organ toxicity – repeated exposure, Category 2
Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 3
H301 Toxic if swallowed
H311 Toxic in contact with skin
H331 Toxic if inhaled
H373 May cause damage to organs through prolonged or repeated exposure
H412 Harmful 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.
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P273 Avoid release to the environment.
P301+P316 IF SWALLOWED: Get emergency medical help immediately.
P321 Specific treatment (see ... on this label).
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P316 Get emergency medical help immediately.
P361+P364 Take off immediately all contaminated clothing and wash it before reuse.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P319 Get medical help if you feel unwell.
P405 Store locked up.
P403+P233 Store in a well-ventilated place. Keep container tightly closed.
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. Artificial respiration may be needed. Refer for medical attention.
Remove contaminated clothes. Rinse skin with plenty of water or shower. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention .
Inhalation or ingestion causes headache, nausea, methemo- globinemia, vomiting, weakness, and stupor; cyanosis caused by contact usually develops in 4-6 hrs.; prolonged and excessive exposure may also cause liver damage. Contact with eyes or skin causes irritation; continued exposure may cause same symptoms as inhalation or ingestion. (USCG, 1999)
INHALATION: Fresh air, rest. Artificial respiration if indicated. Refer for medical attention. SKIN: Remove contaminated clothes. Rinse skin with plenty of water or shower. Refer for medical attention. EYES: First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then take to a doctor.
Extinguish with water, dry chemicals, foam or carbon dioxide.
Special Hazards of Combustion Products: Toxic oxides of nitrogen may form in fire. (USCG, 1999)
Use water spray, powder, foam, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water. Combat fire from a sheltered position.
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. If appropriate, moisten first to prevent dusting. Carefully collect remainder.
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. If appropriate, moisten first to prevent dusting. Carefully collect remainder.
1. Ventilate area of spill. 2. For small quantities, sweep onto paper or other suitable material, place in an appropriate container & burn in a safe place (such as a fume hood). Large quantities may be reclaimed; however, if this is not practical, dissolve in a flammable solvent (such as alcohol) & atomize in a suitable combustion chamber equipped with an appropriate effluent gas cleaning device.
NO open flames. NO contact with combustible substances. Closed system, dust explosion-proof electrical equipment and lighting. Prevent deposition of dust. 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.
Separated from strong acids, strong oxidants, combustible substances, reducing agents and food and feedstuffs.Protect against physical damage to containers and prevent from moisture contacts.
Component | 2-nitroaniline | |||
---|---|---|---|---|
CAS No. | 88-74-4 | |||
Limit value - Eight hours | Limit value - Short term | |||
ppm | mg/m3 | ppm | mg/m3 | |
Finland | 1 | 5,7 | 3 (1) | 17 (1) |
Latvia | ? | 0,5 | ? | ? |
Remarks | ||||
Finland | (1) 15 minutes average value |
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 face shield or eye protection in combination with breathing protection.
Protective gloves. Protective clothing.
Use local exhaust or breathing protection.
no data available
Solid. Powder.
Orange.
Musty
Ca. 74 °C.
284 °C
Combustible. Many reactions may cause fire or explosion.
no data available
167 °C.
970° F (USCG, 1999)
no data available
no data available
no data available
Insoluble in water
log Pow = 1.85. Remarks:Experimental data.
0.003 mm Hg. Temperature:25 °C. Remarks:=0.369 Pa; Experimental data.
0.901 g/cm3. Temperature:25 °C.
4.77 (NTP, 1992) (Relative to Air)
no data available
On combustion, forms toxic fumes of nitrogen oxides. Reacts with strong acids, strong oxidants and strong reducing agents. Reacts with organic materials in the presence of moisture. This generates fire hazard.
no data available
SLIGHT, WHEN EXPOSED TO HEAT OR FLAME.Dust explosion possible if in powder or granular form, mixed with air.O-NITROANILINE may be sensitive to prolonged exposure to light. Mixtures of this chemical with magnesium are hypergolic on contact with nitric acid. It forms extremely explosive addition compounds with hexanitroethane. It has a vigorous reaction with sulfuric acid above 392° F. It is incompatible with acids, acid chlorides, acid anhydrides, chloroformates and strong oxidizers. (NTP, 1992)
no data available
Forms extremely explosive addition compounds with hexanitroethane. Vigorous reaction with sulfuric acid above 200 deg C.
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 may cause effects on the blood. This may result in the formation of methaemoglobin. The effects may be delayed. Medical observation is indicated. See Notes.
The substance may have effects on the blood. This may result in the formation of methaemoglobin. See Notes.
No indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20°C.
AEROBIC: In a 2 week closed bottle biodegradation test, using 100 mg/L substrate and 30 mg/L sludge, 2-nitroaniline had a theoretical BOD of 0%(1). Degradation in a soil mineral salts suspension took greater than 64 days as determined by 100% loss of UV absorbance(2). A 16% BOD threshold was measured with a Warburg respirometer using aniline-acclimated activated sludge(3). A 0% removal (based on chemical oxygen demand) was measured in a batch system using activated sludge and a 5-day incubation period(4). Biological degradation in an electrolytic respirometer using activated sludge was in excess of 10 days(5). 2-Nitroaniline was not biodegradable in an electrolytic respirometer study, although 4-nitroaniline was found to be biodegradable using the same test conditions(6). Aerobic incubation of 2-nitroaniline in a rotary shaker using sewage inocula for 52 days resulted in a maximum loss of 15% as measured by UV absorbance loss(7). A 20-day study using uniformly ring-labeled 2-nitroaniline had a 14-carbon dioxide evolution of 1.9%, measured from laboratory flask system containing a silt loam soil media(8); 14-carbon dioxide evolution was less than 0.3% from the same soil system which had been sterilized with sodium azide(8). 2-Nitroaniline had a biodegradation rate of 0.023/hr in river water giving a half-life of 31 hours, which was classified as poor degradation(9). A 5 day BOD at 20 deg C in Songhua river water was -5% for 2-nitroaniline(10).
A 6 week bioconcentration study obtained BCF values of 2.1-4.9 and <10 for concentrations of 2- nitroaniline of 0.5 and 0.05 mg/L, respectively(1). An aquarium study using carp fish found 2-nitroaniline to have a low bioaccumulation potential(2). A study using zebrafish experimentally determined the BCF for 2-nitroaniline to be 8.1(3). According to a classification scheme(4), these BCF values suggest bioconcentration in aquatic organisms is low(SRC).
The log Koc of 2-nitroaniline was measured as 1.77 giving a Koc of 59(1). According to a classification scheme(2), this Koc value suggests that 2-nitroaniline is expected to have high mobility in soil. 2-Nitroaniline was found to have a Kd value of 8.4 L/kg in homoionic K+ Montmorillonite type soil(3). However, anilines are expected to bind strongly to humus or organic matter in soils due to high reactivity of the aromatic amine group(4,5), suggesting that mobility may be much lower in some soils(SRC).
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: UN1661 (For reference only, please check.)
IMDG: UN1661 (For reference only, please check.)
IATA: UN1661 (For reference only, please check.)
ADR/RID: NITROANILINES (o-, m-, p-) (For reference only, please check.)
IMDG: NITROANILINES (o-, m-, p-) (For reference only, please check.)
IATA: NITROANILINES (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: II (For reference only, please check.)
IMDG: II (For reference only, please check.)
IATA: II (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
Depending on the degree of exposure, periodic medical examination is indicated.Specific treatment is necessary in case of poisoning with this substance; the appropriate means with instructions must be available.See ICSCs 0307 and 0308.