| | 4-Nitrotoluene Basic information |
| | 4-Nitrotoluene Chemical Properties |
| Melting point | 52-54 °C (lit.) | | Boiling point | 238 °C (lit.) | | density | 1.392 g/mL at 25 °C (lit.) | | vapor density | 4.7 (vs air) | | vapor pressure | 5 mm Hg ( 85 °C) | | refractive index | 1.5382 | | Fp | 223 °F | | storage temp. | 2-8°C | | solubility | 0.26g/l | | form | Crystalline Solid | | pka | 11.27 (Perrin, 1972) | | color | Yellow | | Specific Gravity | 1.392 | | explosive limit | 1.6%(V) | | Water Solubility | 0.35 g/L (20 ºC) | | Merck | 14,6650 | | BRN | 1906911 | | Henry's Law Constant | 5.64 at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999) | | Exposure limits | NIOSH REL: TWA 2 ppm (11 mg/m3), IDLH 200 ppm; OSHA PEL: TWA 5
ppm (30 mg/m3); ACGIH TLV: TWA 2 ppm (adopted). | | Stability: | Stability May be shock sensitive. Incompatible with sulfuric acid, strong bases, reducing agents, strong oxidizing agents. | | InChIKey | ZPTVNYMJQHSSEA-UHFFFAOYSA-N | | LogP | 2.37 at 25℃ | | CAS DataBase Reference | 99-99-0(CAS DataBase Reference) | | IARC | 3 (Vol. 65) 1996 | | NIST Chemistry Reference | Benzene, 1-methyl-4-nitro-(99-99-0) | | EPA Substance Registry System | p-Nitrotoluene (99-99-0) |
| | 4-Nitrotoluene Usage And Synthesis |
| Chemical Properties | light yellow crystals | | Chemical Properties | Nitrotoluene is formed in 3 isomeric forms.
The o-and m-forms are yellow liquids or solids. The p-form
is a pale yellow crystalline solid. All have weak aromatic
odors. The Odor Thresholds are: 0.05 mg/L (o-isomer);
1.74 ppm (m-isomer). | | Uses | used in the synthesis of
dyestuffs, explosives, and agricultural chemicals | | Uses | 4-Nitrotoluene is an explosive material. | | Uses | manufacture of dyes, toluidines, nitrobenzoic acids, agricultural and rubber chemicals. | | Definition | ChEBI: 4-nitrotoluene is a mononitrotoluene that consists of toluene bearing a nitro substituent at the 4-position. | | Synthesis Reference(s) | Journal of the American Chemical Society, 79, p. 5528, 1957 DOI: 10.1021/ja01577a053
Tetrahedron Letters, 29, p. 97, 1988 DOI: 10.1016/0040-4039(88)80026-1 | | General Description | A yellow liquid with a weak aromatic odor. Toxic. Insoluble in water. Combustible but may take some effort to ignite. Produces toxic oxides of nitrogen when burned. In a spill, immediate steps should be taken to limit its spread to the environment. Can easily penetrate the soil and contaminate groundwater or nearby streams. Used to make other chemicals. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | 4-Nitrotoluene may react violently with sodium, tetranitromethane, strong oxidizing agents , sulfuric acid and other acids. | | Hazard | Toxic by inhalation, ingestion, skin absorption. Methemoglobinemia. Questionable carcinogen. | | Health Hazard | INHALATION, INGESTION, OR SKIN: Headache, flushed face, dizziness, dyspnea (difficult breathing), cyanosis, nausea, vomiting, muscular weakness, rapid pulse and respiration, irritability, and convulsions. | | Fire Hazard | Special Hazards of Combustion Products: Yields toxic oxides of nitrogen when burning. | | Safety Profile | A poison. Moderately
toxic by ingestion, inhalation, and
intraperitoneal routes. Mildly toxic by skin
contact. Mutation data reported.
Combustible when exposed to heat or
flame. To fight fire, use CO2, dry chemical,
foam. The residue from vacuum distillation
may explode spontaneously. Reacts with
sodmm to form an ignitable product.
Violent reaction with concentrated sulfuric
acid (above 16O°C), sulfuric acid + sulfur
trioxide (above 52°C). Mixtures with
tetranitromethane are sensitive high
explosives. May explode on standing. It has
been involved in plant scale explosions.
When heated to decomposition it emits
toxic fumes of NOx. See also other
methylnitrobenzene entries and NITRO
COMPOUNDS OF AROMATIC
HYDROCARBONS. | | Potential Exposure | The nitrotoluenes are used in the
production of toluidines and other dye intermediates.
All isomers are used in manufacture of agriculture and
rubber chemicals and in various dyes. | | Environmental fate | Biological. Under anaerobic conditions using a sewage inoculum, 3- and 4-nitrotoluene both
degraded to toluidine (Hallas and Alexander, 1983). Robertson et al. (1992) reported that toluene
dioxygenases from Pseudomonas putida F1 and Pseudomonas sp. Strain JS 150 oxidized the
methyl group forming 2-methyl-5-nitrophenol and 3-methyl-6-nitrocatechol.
Chemical. Though no products were identified, 4-nitrotoluene (1.5 x 10-5 M) was reduced by
iron metal (33.3 g/L acid washed 18 to 20 mesh) in a carbonate buffer (1.5 x 10-2 M) at pH 5.9 and
15 °C. Based on the pseudo-first-order disappearance rate of 0.0335/min, the half-life was 20.7
min (Agrawal and Tratnyek, 1996). | | Shipping | UN1664 Nitrotoluenes, (o-; m-; p-), Hazard
Class: 6.1; Labels: 6.1-Poisonous materials. | | Purification Methods | Dry it in air, then dry it in a vacuum desiccator over H2SO4. [Wright & Grilliom J Am Chem Soc 108 2340 1986, Beilstein 5 IV 848.] | | Incompatibilities | Decomposes on contact with strong oxidizers;
strong acids; reducing agents; strong bases; ammonia,
amines producing toxic fumes, causing fire and explosion
hazard. Heat above 190C may cause explosive decomposition.
Attacks some plastics, rubbers, and coatings. | | Waste Disposal | Controlled incineration-care
must be taken to maintain complete combustion at all
times. Incineration of large quantities may require scrubbers
to control the emission of nitrogen oxides. |
| | 4-Nitrotoluene Preparation Products And Raw materials |
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