Product Details:
Minimum Order Quantity250 Kilogram
ApplicationPaint Solvents, Agro, etc.
Packaging TypeDrum (Barrels) & Tanker
Packaging Size250 Kgs Drum (Barrel) & Tanker load.
Grade StandardTechnical Grade
BrandAkshar Group
H.S. Code29042010
CAS No.98-95-3

Manufacturers and Suppliers of nitro benzene mumbai

akshar international is one of the largest chemical supplier and manufacturer in mumbai. we provides a list of chemicals also we provide one of the best quality nitro benzene. we provide nitro benzene with Minimum Order Quantity 250kg online. which really Used as Paint Solvents, Agro, etc.

Here some important information about nitro benzene.


Nitrobenzene is a natural compound with the concoction equation C6H5NO2. It is a water-insoluble light yellow oil with an almond-like smell. It stops to give greenish-yellow precious stones. It is delivered on a substantial scale from benzene as an antecedent to aniline. In the research facility, it is once in a while utilized as a dissolvable, particularly for electrophilic reagents.


Nitrobenzene is set up by nitration of benzene with a blend of concentrated sulfuric corrosive, water, and nitric corrosive. This blend is some of the time called “blended corrosive.” The creation of nitrobenzene is a standout amongst the most risky procedures directed in the substance business as a result of the exothermicity of the response (ΔH = −117 kJ/mol).[3]

Benzol.svg + Nitronium particle vert.svg


Rightward response bolt with minor product(s) to upper right


World limit with respect to nitrobenzene in 1985 was about 1.7×106 tonnes.[3]

The nitration procedure includes arrangement of the nitronium particle (NO2+), trailed by an electrophilic fragrant substitution response of it with benzene. The nitronium particle is produced by the response of nitric corrosive and an acidic parchedness specialist, ordinarily sulfuric corrosive:

HNO3 + H+ ⇌ NO2+ + H2O


Around 95% of nitrobenzene is devoured in the creation of aniline:[3]

C6H5NO2 + 3 H2 → C6H5NH2 + 2 H2O

Aniline is a forerunner to urethane polymers, elastic synthetic concoctions, pesticides, colors (especially azo colors), explosives, and pharmaceuticals.

Most aniline is expended in the generation of methylenedianiline, a forerunner to polyurethanes.

Particular applications of nitro benzene

Nitrobenzene is likewise used to veil horrendous scents in shoe and floor shines, calfskin dressings, paint solvents, and different materials. Redistilled, as oil of mirbane, nitrobenzene had been utilized as a modest fragrance for cleansers. It has been substituted by less poisonous synthetic concoctions for this purpose.[4] A noteworthy trader advertise for nitrobenzene is its utilization in the generation of the pain relieving paracetamol (otherwise called acetaminophen) (Mannsville 1991).[5] Nitrobenzene is additionally utilized in Kerr cells, as it has an abnormally vast Kerr consistent. Proof recommends its utilization in horticulture as a plant development/blooming stimulant.[6]

Natural responses

Beside its transformation to aniline, nitrobenzene can be specifically decreased to azoxybenzene,[7] azobenzene,[8] nitrosobenzene,[9] hydrazobenzene,[10] and phenylhydroxylamine.[11]


Nitrobenzene is profoundly harmful (Threshold Limit Value 5 mg/m3) and promptly consumed through the skin.

Drawn out presentation may make genuine harm the focal sensory system, weaken vision, cause liver or kidney harm, weakness and lung disturbance. Inward breath of vapors may actuate cerebral pain, sickness, weariness, tipsiness, cyanosis, shortcoming in the arms and legs, and in uncommon cases might be lethal. The oil is promptly retained through the skin and may build pulse, cause seizures or infrequently passing. Ingestion may comparatively cause cerebral pains, tipsiness, sickness, retching and gastrointestinal bothering, loss of sensation/use in appendages and furthermore causes interior bleeding.[9]

Nitrobenzene is viewed as a conceivable human cancer-causing agent by the United States Environmental Protection Agency,[12] and is characterized by the IARC as a Group 2B cancer-causing agent which may be “perhaps cancer-causing to humans”. It has been appeared to cause liver, kidney, and thyroid adenomas and carcinomas in rats.

It is delegated an amazingly unsafe substance in the United States as characterized in Section 302 of the U.S. Crisis Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is liable to strict detailing necessities by offices which produce, store, or use it in critical quantities.

Mainstream culture

The 1927 short story The Avenging Chance by Anthony Berkeley talks about contemporary employments of nitrobenzene. It is additionally at the focal point of the plot in Berkeley’s The Poisoned Chocolates Case of 1929.

In the 1937 Nero Wolfe investigator novel The Red Box by Rex Stout, an individual is killed by having oil of mirbane spilled on him in his vehicle.

In Belfast, amid the Troubles’ Bloody Friday (1972), the bombs utilized contained clocks fastened to sacks loaded with nitrobenzene.


NIOSH Pocket Guide to Chemical Hazards. “#0450”. National Institute for Occupational Safety and Health (NIOSH).

“Nitrobenzene”. Quickly Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

Corner G (2007). “Nitro Compounds, Aromatic”. Ullmann’s Encyclopedia of Industrial Chemistry (sixth ed.). Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 978-3-527-30385-4.

Hogarth CW (January 1912). “an instance of harming by oil of mirbane (nitro-benzol)”. English Medical Journal. 1 (2665): 183. PMC 2344391. PMID 20765985.

Bhattacharya A, Purohit VC, Suarez V, Tichkule R, Parmer G, Rinaldi F (March 2006). “One-advance reductive amidation of nitro arenes: application in the union of Acetaminophen”. Tetrahedron Letters. 47 (11): 1861– 1864. doi:10.1016/j.tetlet.2005.09.196.

“Blooming stimulant organization utilizing nitrobenzene”.

Bigelow, H. E.; Palmer, Albert. “Azoxybenzene”. Natural Syntheses.; Collective Volume, 2, 1943, p. 57

Bigelow HE, Robinson DB (1955). “Azobenzene”. Natural Syntheses.; Collective Volume, 3, p. 103

Coleman GH, McCloskey CM, Stuart FA. “Nitrosobenzene”. Natural Syntheses.; Collective Volume, 3, p. 668

Karwa, Shrikant L.; Rajadhyaksha, Rajeev A. (January 1988). “Particular synergist hydrogenation of nitrobenzene to hydrazobenzene”. Modern and Engineering Chemistry Research. 27 (1): 21– 24. doi:10.1021/ie00073a005. ISSN 0888-5885.

Kamm O. “β-Phenylhydroxylamine”. Natural Syntheses.; Collective Volume, 1, p. 445

Division, US EPA, ORD, Integrated Risk Information System. “Nitrobenzene CASRN 98-95-3 – IRIS – US EPA, ORD”. Recovered 10 August 2017.

“Operators Classified by the IARC Monographs, International Agency for Research on Cancer” (PDF). Recovered 10 August 2017.