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2,4-Dinitrotoluene

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2,4-Dinitrotoluene - Names and Identifiers

Name 2,4-Dinitrotoluene
Synonyms 2,4-DNT
NCI-C01865
Dinitrotoluol
DINITROTOLUENE
2,4-Dinitrotoluene
rcrawastenumberu105
toluene,2,4-dinitro-
Toluene, 2,4-dinitro-
dinitrotoluenes,molten
Rcra waste number U105
1-methyl-2,3-dinitrobenzene
1-Methyl-2,4-dinitrobenzene
CAS 121-14-2
EINECS 204-450-0
InChI InChI=1/C7H6N2O4/c1-5-3-2-4-6(8(10)11)7(5)9(12)13/h2-4H,1H3
InChIKey RMBFBMJGBANMMK-UHFFFAOYSA-N

2,4-Dinitrotoluene - Physico-chemical Properties

Molecular FormulaC7H6N2O4
Molar Mass182.13
Density1,521 g/cm3
Melting Point67-70°C(lit.)
Boling Point300 °C
Flash Point155 °C
Water Solubility0.3 g/L (20 ºC)
Solubility Soluble in acetone, ethanol, benzene, ether, and pyrimidine (Weast, 1986)
Vapor Presure1 mm Hg ( 102.7 °C)
Appearanceneat
BRN1912834
pKa13.53 (Perrin, 1972)
Storage Condition2-8°C
StabilityStable. Incompatible with oxidizing agents, reducing agents, strong bases.
Refractive Index1.4420
Physical and Chemical Properties

trait yellow needle crystal or monoclinic prisms. Industrial products are oily liquids.
melting point 67~70 ℃
boiling point 300 ℃ (decomposition)
relative density 1.3208
solubility: soluble in benzene, slightly soluble in carbon disulfide, slightly soluble in ether, cold ethanol, very slightly soluble in water.

UseUsed as a raw material for organic synthesis, dyes and explosives

2,4-Dinitrotoluene - Upstream Downstream Industry

Raw MaterialsToluene
Nitric acid

2,4-Dinitrotoluene - Nature

Open Data Verified Data

light yellow, darker in the sun, and red in contact with alkali. Toxic, flammable. Vapor pressure 13. 33kPa/157.7 °c; Flash point 207 °c; Melting point 69.5 °c; Boiling point 300 °c. Slightly soluble in water, ethanol, ether, soluble in benzene, acetone and other organic solvents. Dinitrotoluene has certain chemical activity, can be decomposed by heat, and can be hydrolyzed in water. It is flammable in case of open flame and high heat. It is mixed with an oxidizing agent to form an explosive mixture. Combustion or explosion may be caused by friction, shock, or impact. A large amount of smoke is produced during combustion.

Last Update:2025-06-10 22:55:16

2,4-Dinitrotoluene - Preparation Method

Open Data Verified Data

O-nitrotoluene or p-nitrotoluene is nitrated by mixed acid to produce dinitrotoluene, and the reaction product is separated, washed with water and distilled to obtain a finished product.

Last Update:2022-01-01 10:50:46

2,4-Dinitrotoluene - Application

Open Data Verified Data

DNT is an important explosive and a starting material for the preparation of 2,4-= nitrotoluene. Can also be used in polyurethane, dyes, medicine, rubber and other organic synthesis industry.

Last Update:2025-08-19 16:24:40

2,4-Dinitrotoluene - Safety

Open Data Verified Data

highly toxic. With carcinogenicity. Rat oral LD50:268mg/kg. This product can cause methemoglobinemia. Staff should be well protected, if accidentally touch the eyes and skin, should immediately rinse with flowing water. Toxic to aquatic organisms, the concentration of 10 mg/L, can cause the death of fish and aquatic organisms. Extremely flammable and explosive. When there is a fire, use a dry powder, foam and other fire extinguishing, and water spray cooling container wall.

Last Update:2022-01-01 10:13:36

2,4-Dinitrotoluene - Reference Information

Henry's Law Constant5.39(x 10-8 atm?m3/mol) at 25 °C (thermodynamic method-GC/UV spectrophotometry, Altschuh et al., 1999)
(IARC) carcinogen classification 2B (Vol. 65) 1996
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Uses Used as a raw material for organic synthesis, dyes and explosives
2,4-dinitrotoluene can be derived from a series of intermediates, such as: These intermediates are used to produce sulphide yellow GC, sulphide yellow brown 5G, sulphide yellow brown 6G, sulphide red brown B3R and other dyes, produce explosive TNT, and produce 2,4-toluene diisocyanate. The amount of toluene diisocyanate in these intermediates is large, mainly used for bulk products such as polyurethane foam, polyurethane elasticity, polyurethane coatings, etc.
production method 1. obtained from nitration of p-nitrotoluene: nitration waste acid (sulfuric acid concentration is 77%) is added to the nitration kettle, then melted p-nitrotoluene is added and stirred to reduce the temperature in the kettle to about 55 ℃. Then the mixed acid (composed of 31.75% nitric acid and 64.85% sulfuric acid) is added in two batches. The first batch of feeding temperature is 52-56 ℃, and the second batch of feeding process temperature gradually rises from 54 ℃ to 70 ℃, about 6-7h after feeding, and the reaction continues at 75 ℃ for nearly 3h. After the reaction is completed, add cold water to dilute under stirring, and let it stand for cooling. After the upper reactants are completely solidified, the waste acid is released (part of it is applied). Heat and melt the reactant again, stir it a little and let it stand for cooling. After the reactant solidifies, put the waste acid again. The reactants were melted and neutralized with liquid alkali at 68-70°C to a pH of 5-6. Spray cold water to cool down, cool to 35 ℃, filter and wash with water to obtain 2, 4-dinitrotoluene. Raw material consumption quota: p-nitrotoluene 774kg/t, sulfuric acid (95.5%)785kg/t, nitric acid (98%)362kg/t. 2. Nitration of toluene: crude nitrotoluene containing o-nitrotoluene 62-63%, p-nitrotoluene 33-34% and m-nitrotoluene 3-4% was obtained in 97% yield. Mixed acid is added dropwise to this crude nitrotoluene. Stirring, nitrification reaction in 98.6% yield to obtain crude dinitrotoluene (CAS number [25321-14-6], is a mixture of three isomers). The general situation of material balance in nitrification process is as follows. Dissolve the dinitrotoluene mixture in methanol or ethanol, then cool, crystallize, separate and distill 2, 4-dinitrotoluene to obtain 2, 4-dinitrotoluene. The former method is mainly used to produce pure 2,4-dinitrotoluene, I .e. nitration of p-nitrotoluene, and the purity of industrial products is ≥ 95%.
category flammable solids
toxicity classification poisoning
acute toxicity oral-rat LD50: 268 mg/kg; Oral-mouse LD50: 790 mg/kg
stimulation data skin-rabbit 500 mg/24 hours mild
explosive hazard characteristics blastable when mixed with oxidant
flammability hazard characteristics flammable in case of open flame, high temperature and oxidant; toxic nitrogen oxide smoke from combustion
storage and transportation characteristics warehouse ventilation and low temperature drying; Store separately from oxidants and acids
fire extinguishing agent water, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent
occupational standard TWA 1.5 mg/m3
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-10 22:29:15
2,4-Dinitrotoluene
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2,4-Dinitrotoluene
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Raw Materials for 2,4-Dinitrotoluene
Toluene
Nitric acid
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