2-Nitrotoluene

 

Product Name: 2-Nitrotoluene

Synonyms: O-NITROTOLUENE;o-nitrophenylmethane;1-methyl-2-nitro-benzen;Benzene,1-methyl-2-nitro-;2-NITROTOLUENE,1X1ML, ACN 1000UG/ML;2-NITROTOLUENE OEKANAL, 250 MG;2-NITROTOLUENE, 1000MG, NEAT;2-NitroTolueneForSynthesis

CAS: 88-72-2

MF: C7H7NO2

MW: 137.14

EINECS: 201-853-3

Product Categories: Intermediates of Dyes and Pigments;2-MethyInitrobenzene;Organics;8000 Series Solidwaste Methods;Analytical Standards;AromaticsEnvironmental Standards;Chemical Class;Environmental Standards;ExplosivesEPA;Method 8330Alphabetic;N;NA - NIAnalytical Standards;Nitro CompoundsChromatography;Solid WasteMore...Close...;-;Volatiles/ Semivolatiles

Mol File: 88-72-2.mol

2-Nitrotoluene Structure

2-Nitrotoluene Chemical Properties

Melting point -9 °C

Boiling point 225 °C(lit.)

density 1.163 g/mL at 25 °C(lit.)

vapor pressure 0.1 hPa (20 °C)

refractive index n20/D 1.546(lit.)

Fp 223 °F

storage temp. 2-8°C

solubility 0.65g/l (experimental)

form Liquid

color Clear yellow to yellow-green

PH 6-8 (H2O)

explosive limit 1.47-8.8%(V)

Water Solubility 0.44 g/L (20 ºC)

Merck 14,6650

BRN 1907580

Henry's Law Constant 1.25 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: Stable. Combustible. Incompatible with oxidizing agents, strong bases, sulfuric acid, reducing agents, hydrogen, sodium.

InChIKey PLAZTCDQAHEYBI-UHFFFAOYSA-N

CAS DataBase Reference 88-72-2(CAS DataBase Reference)

NIST Chemistry Reference Benzene, 1-methyl-2-nitro-(88-72-2)

EPA Substance Registry System o-Nitrotoluene (88-72-2)

Safety Information

Hazard Codes T,N,F

Risk Statements 45-46-22-51/53-62-36/37/38-23/24/25-11-36-20/21/22

Safety Statements 53-45-61-27-16-36/37-26

RIDADR UN 1664 6.1/PG 2

WGK Germany 3

RTECS XT3150000

Autoignition Temperature 420 °C

TSCA Yes

HazardClass 6.1

PackingGroup II

HS Code 29042000

Hazardous Substances Data 88-72-2(Hazardous Substances Data)

Toxicity LD50 orally in Rabbit: 891 mg/kg

MSDS Information

Provider Language

alpha-Methylnitrobenzene English

SigmaAldrich English

ACROS English

ALFA English

2-Nitrotoluene Usage And Synthesis

Overview O-nitrotoluene is also known as 2-nitrotoluene or 1-methyl-2-nitrobenzene，and is yellow oily transparent liquid. It has the smell of nitrobenzene. The relative density is 1.1629. The melting point is-2.9℃ (α-type, stable type),-9.5℃ (β-type, non-stable type). The boiling point is 221.7 °C, 118 °C (2.133×103Pa) and 50.0 °C (0.133×103Pa). The flash point is 106.1 °C (closed system). The refractive index is 1.5450. The viscosity is 0.0262 mPa•s (15℃). The vapor pressure (×103 Pa) is 10.906 (5℃), 12.639 (10℃), 14.612 (20℃), 15.892 (30℃). It is slightly soluble in water (0.061 at 30°C), soluble in benzene, chloroform and petroleum ether and immiscible with ethanol and ether. It can evaporate together with water vapor. Due to the strong electron-withdrawing ability of nitro group, the methyl of is easy to be oxidized to form o-nitrobenzaldehyde or o-nitrobenzoic acid according to oxidation conditions. And o-nitrotoluene can be reduced in the presence of catalyst to generate o-toluidine, which can generate 2,4 or 2,6 dinitrotoluene after further nitration. O-nitrotoluene can also be chlorinated to generate nitrobenzyl chloride. In addition, o-nitrotoluene can also generate azo compounds. LD50 (rat oral) is 801mg/kg.

O-nitrotoluene is mainly used as the raw material of dyestuffs to prepare 4-chloro-2-nitrotoluene, 6-chloro-2-nitrotoluene, o-toluidine, o-tolidine, 2,6-dichlorobenzaldehyde and other dyestuffs intermediates, in which 4-chloro-2-nitrotoluene is a pharmaceutical raw material and o-toluidine is the raw material of pesticide fungicides and spices. O-nitrotoluene is a pharmaceutical raw material to prepare 2,2'-dinitrobenzene, o-nitrobenzyl bromide, bromine alkane and other medicines, and is also the raw material to prepare indole to be used as amino acids and plant growth regulators. O-nitrotoluene is the raw material to prepare dinitrotoluene to be used as powder. O-toluidine can also be used as vulcanization accelerator and to prepare o-nitrobenzoic acid as pharmaceutical raw material.

Chemical Properties Yellow flammable liquid; insoluble in water; soluble in chloroform and benzene; immiscible with ethanol and ethyl ether.

Application Used for the intermediates of dyes and pesticides, and also for the production of coatings, plastics and pharmaceuticals. O-nitrotoluene is mainly used in the production of o-toluidine, o-tolidine, and also used as the important raw materials of dyes, paints, plastics and pharmaceutical. In the pharmaceutical industry, it is used for the production of nifedipine, tegretol, imipramine hydrochloride, bromide has hydrochloride amine and sodium dicloxaeillin.I can also be used for dyes, pharmaceuticals, pesticides, plastics and other industries.

Production method Nitrify toluene with mixed acid to generate mixed nitrotoluene, which mainly consists of o-nitrotoluene (about two-thirds) and p-nitrotoluene (about one-third). The mixed nitrotoluene can be separated to get the pure product. Add toluene to the reactor and cool to below 25℃. Then add the mixed acid (ie, 25-30% of nitric acid, 55-58% of sulfuric acid and 20-21% of water) and control the temperature not exceeding 50℃. Stir for 1-2h, and then stand for 6h. Separate the generated nitrotoluene, and wash them with water and alkali liquor to remove unreacted toluene and aliphatic compound. The crude nitrotoluene products consist of 55-60% of o-nitrotoluene, 2-5% of m-nitrotoluene and 35-40% of p-nitrotoluene, with a yield of 90-95%. The various isomers can be separated by crude distillation and crystallization according to the difference of the boiling point and melting point. Namely, first distill the crude nitrotoluene under vacuum to separate out the majority of o-nitrotoluene. And then the residual fraction containing more p-nitrotoluene is separated by vacuum distillation, and cooled for crystallization and separated to obtain the finished products. The tarry substance with high boiling point remains in the still. M-nitrotoluene remains in the mother liquor separated out the p-nitrotoluene, and can be obtained by rectification after repeated accumulation. The purity of ortho and para nitrotoluene can respectively reach 98% and 99%. The domestic process is the two-pot series process, and the reaction temperature of the main pot is 40-45℃ and the second pot is 50-55℃. The preparation of mixed acid is roughly similar, including 26-28% of nitric acid, 56-57% of sulfuric acid and 16-18% of water. The raw material consumption quota: toluene (98%) 800kg/t, nitric acid (98%) 470kg/t, sulfuric acid (92.5%) 450kg/t, caustic soda (42%) 100kg /t

Category Toxic substance

Toxicity classification moderate toxicity

Acute toxicity Oral-Rat LD50: 891 mg/kg; Oral-mouse LD50: 970 mg/kg

Explosives hazardous characteristics Explore when mixing with air; explore itself when meeting heat

Flammability Hazardous properties Combust when meeting open fire; Combustion produces toxic nitrogen oxide fumes.

Storage and transportation characteristics Stored in the low-temperature, well-ventilated and dry warehouse and stored separately with oxidants and food additives.

Fire extinguishing agent mist water, foam, carbon dioxide

Occupational Standard TWA 28 mg/m3; STEL 58 mg/m3

Description o-Nitrotoluene is a yellow-coloured liquid. It is used for the synthesis of a variety of industrial products. These include to synthesise agricultural and rubber chemicals, azo and sulphur dyes, and dyes for cotton, wool, silk, leather, and paper. O-nitrotoluene decomposes on contact with strong oxidants, reducing agents, acids, or bases producing toxic fumes, nitrogen oxides, and carbon monoxide.

Chemical Properties light yellow to darker yellow-green liquid

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).

Physical properties Clear, colorless to pale yellowish combustible liquid with a faint, aromatic odor. May darken on exposure to air.

Uses 2-Nitrotoluene may be employed as nitrogen supplement in the culture medium of Pseudomonas sp. strain ClS1. It may be employed as carbon and energy supplement in the culture medium of Pseudomonas sp. strain JS42

Definition ChEBI: A mononitrotoluene that is toluene carrying a nitro substituent at position 2.

General Description Light yellow oily liquid with a characteristic odor of aromatic nitro compounds. Sinks in water. Derived from toluene by nitration and separation by fractional distillation. Flash point 223°F.

Air & Water Reactions Insoluble in water.

Reactivity Profile 2-Nitrotoluene is toxic by inhalation, ingestion and skin aborption, targeting the blood, central nervous system, skin, and gastrointestinal tract. Symptoms include, anoxia, weakness or dizziness, nausea and vomiting. If 2-Nitrotoluene contacts the eye, the eye should be irrigated immediately. If 2-Nitrotoluene contacts the skin, the area should be washed with soap. If inhaled, respiratory support should be administered. Finally, if ingested, medical attention should be sought. 2-Nitrotoluene also reacts with sulfuric acid, sodium hydroxide, hydrogen, sodium, tetranitromethane, reducing agents and strong oxidizers. 2-Nitrotoluene is very heat sensitive.

Hazard Toxic by inhalation, ingestion, skin absorption. Methemoglobinemia. Probable carcinogen.

Health Hazard INHALATION, INGESTION, OR SKIN: Headache, flushing of face, dizziness, dyspnea (difficult breathing), cyanosis, nausea, vomiting, muscular weakness, increased pulse and respiratory rate, irritability, and convulsions. SKIN: Irritation.

Safety Profile Confirmed carcinogen. A poison. Moderately toxic by ingestion. Mucous membrane effects by inhalation. Mutation data reported. Combustible when exposed to heat or open flame. To fight fire, use water spray, fog, foam, CO2. Potentially explosive reaction with alkali (e.g., sodmm hydroxide). 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.

Carcinogenicity o-Nitrotoluene is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimental animals and supporting data on mechanisms of carcinogenesis.

Environmental fate Biological. Robertson et al. (1992) reported that toluene dioxygenases from Pseudomonas putida F1 and Pseudomonas sp. Strain JS 150 oxidized the methyl group forming 2-nitrobenzyl alcohol.

Shipping UN1664 Nitrotoluenes, (o-; m-; p-), Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Purification Methods Crystallise 2-nitrotoluene (repeatedly) from absolute EtOH by cooling in a Dry-ice/alcohol mixture. Further purify it by passing an alcoholic solution through a column of alumina. [Beilstein 5 IV 845.]

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.

2-Nitrotoluene Preparation Products And Raw materials

Preparation Products o-Toluidine-->4-Nitrotoluene-->Indole-->2,6-Dichlorotoluene-->2,4-Dichlorotoluene-->3-Nitrotoluene-->2-(CYANOMETHYL)-BENZENESULFONAMIDE-->2-Nitrobenzaldehyde-->3-Chloro-2-methylaniline-->Quinclorac-->2,4-Dinitrotoluene-->4-Chloro-2-nitrotoluene-->2-Chloro-6-nitrotoluene-->Nifedipine-->5-chloro-2-methylbenzenediazonium -->Dibenz[b,f]azepine-5-carbonyl chloride-->5-Methylphenazinium methosulfate-->5-Chloro-2-methylaniline-->Dicloxacillin sodium-->2-Nitrobenzoic acid-->2-Nitrobenzyl bromide-->2,6-Dinitrotoluene-->2-Nitrobenzyl alcohol-->Carbamazepine-->Iminodibenzyl