3-Nitrotoluene

3-Nitrotoluene Basic information
Product Name:3-Nitrotoluene
Synonyms:3-NITROTOLUENE;3-METHYLNITROBENZENE;m-mononitrotoluene;m-nitro-toluen;MNT;nsc9578;Toluene, m-nitro-;toluene,3-nitro-
CAS:99-08-1
MF:C7H7NO2
MW:137.14
EINECS:202-728-6
Product Categories:Environmental Standards;ExplosivesEPA;N;Nitro CompoundsChromatography;Solid WasteMore...Close...;Volatiles/ Semivolatiles;Industrial/Fine Chemicals;Aromatic Hydrocarbons (substituted) & Derivatives;Organics;Method 8330Alphabetic;NA - NIAnalytical Standards;8000 Series Solidwaste Methods;Analytical Standards;AromaticsEnvironmental Standards;Chemical Class
Mol File:99-08-1.mol
3-Nitrotoluene Structure
3-Nitrotoluene Chemical Properties
Melting point 15 °C
Boiling point 230-231 °C(lit.)
density 1.157 g/mL at 25 °C(lit.)
vapor density 4.73 (vs air)
vapor pressure 1 mm Hg ( 50.2 °C)
refractive index n20/D 1.541(lit.)
Fp 215 °F
storage temp. 2-8°C
solubility 0.419g/l
form Liquid
color Clear yellow to yellow-brownish
explosive limit2.2%(V)
Water Solubility insoluble
Merck 14,6650
BRN 1906910
Henry's Law Constant9.31 at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999)
Exposure limitsNIOSH 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 reducing agents, strong oxidizing agents, strong bases.
LogP2.4
CAS DataBase Reference99-08-1(CAS DataBase Reference)
IARC3 (Vol. 65) 1996
NIST Chemistry ReferenceBenzene, 1-methyl-3-nitro-(99-08-1)
EPA Substance Registry Systemm-Nitrotoluene (99-08-1)
Safety Information
Hazard Codes T,F,Xn
Risk Statements 23/24/25-33-51/53-36/37/38-11-36-20/21/22
Safety Statements 36/37-45-61-37-28A-27-16-26
RIDADR UN 1664 6.1/PG 2
WGK Germany 2
RTECS XT2975000
TSCA Yes
HazardClass 6.1
PackingGroup II
HS Code 29042000
Hazardous Substances Data99-08-1(Hazardous Substances Data)
ToxicityAcute oral LD50 for guinea pigs 3,600 mg/kg, mice 330 mg/kg, rats 1,072 mg/kg, rabbits 2,400 (quoted, RTECS, 1985).
MSDS Information
ProviderLanguage
m-Nitrophenylmethane English
SigmaAldrich English
ACROS English
ALFA English
3-Nitrotoluene Usage And Synthesis
Chemical PropertiesNitrotoluene 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 properties3-Nitrotoluene is a light yellow oily liquid with a nitrobenzene-like odor. The relative density is 1.1571, the melting point is 16°C, and the boiling point is 230-231°C. Almost insoluble in water, soluble in ethanol, ether, chloroform and benzene. Can volatilize with water vapor.
Uses3-Nitrotoluene is mainly used in organic synthesis as an intermediate for pesticides, dyes, explosives, medicines, color developers, plastics, synthetic fibers and auxiliaries.
Preparation3-Nitrotoluene is obtained by fractional distillation and purification after nitration of toluene with mixed acid below 50℃. Toluene nitration can get different products with different reaction conditions and catalysts, such as o-nitrotoluene, p-nitrotoluene, m-nitrotoluene, 2,4-dinitrotoluene and 2,4,6-trinitrotoluene Toluene etc.
DefinitionChEBI: 3-nitrotoluene is a mononitrotoluene carrying a nitro group at position 3.
General DescriptionYellow crystals that melt at 59°F to a yellow liquid. Often therefore encountered as a liquid. Flash point 223°F. Boiling point 450°F. Insoluble in water. Toxic by inhalation and ingestion.
Air & Water ReactionsInsoluble in water.
Reactivity Profile3-Nitrotoluene reacts with sulfuric acid, strong oxidizing agents and reducing agents.
HazardToxic by inhalation, ingestion, skin absorption. Methemoglobinemia. Probable carcinogen.
Health HazardINHALATION, INGESTION OR SKIN ABSORPTION: Headache, flushing of face, dizziness, difficult breathing, cyanosis, nausea, vomiting, muscular weakness, increased pulse and respiratory rate, irritability and convulsions. EYES: Slight irrita- tion. SKIN: Slight irritation.
Potential ExposureThe 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 fateBiological. Under anaerobic conditions using a sewage inoculum, 3-nitrotoluene 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 3-nitrobenzyl alcohol.
ShippingUN1664 Nitrotoluenes, (o-; m-; p-), Hazard Class: 6.1; Labels: 6.1-Poisonous materials.
Purification MethodsDry 3-nitrotoluene over P2O5 for 24hours, then fractionally distil it under reduced pressure. [Clark & Taylor Org. Synth Coll Vol I 415 1941, Beilstein 5 IV 847.]
IncompatibilitiesDecomposes 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 DisposalControlled 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.
2,4-Dichloro-5-trifluoromethyl-3-nitrotoluene Methyl 3-BROMO-2-NITROTOLUENE 2-(1,1,2,2-TETRAFLUOROETHOXY)-5-NITROTOLUENE,2-(1,1,2,2-TETRAFLUOROETHOXY)-5-NITROTOLUENE ETHYLENEDIAMINE TETRAKIS(PROPOXYLATE-BLOCK-ETHOXYLATE) TETROL Diphenolic acid Trinitrotoluene mixed with aluminium Cyelotrimethylenetrinitramine and trinitrotoluene, aluminium powder mixtures ALPHA-BROMO-3-IODO-4-NITROTOLUENE,ALPHA-BROMO-3-IODO-4-NITROTOLUENE 5-Chlorovaleric acid 2-Fluoro-3-nitrotoluene TRITON Nitrotoluol 5-Nitroso-2-cresol Trinitrotoluene and nitronaphthalene mixtures O-NITROTOLUENE (RING-13C6),O-NITROTOLUENE (RING-13C6) Trinitrotoluene and hexanitro-1,2-diphenylethene mixtures Trinitrotoluene and trinitrobenzene and bexanitro-1,2-diphenylethene mixtures

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