Product Details:
Minimum Order Quantity250 Kilogram
ApplicationDyes, Basic Pharma, Pigments, Agro Chemicals, Molymer etc.
Packaging TypeDrum (Barrels) & Tanker
Packaging Size250 Kgs Drum (Barrel) & Tanker load.
BrandAkshar Group
H.S. Code29039110
CAS No.108-90-7

Manufacturers and Suppliers of mono chloro benzene (mcb) 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 mono chloro benzene (mcb). we provide mono chloro benzene (mcb) with Minimum Order Quantity 250kg online. which really Used as Dyes, Basic Pharma, Pigments, Agro Chemicals, Molymer etc.

Here some important information about mono chloro benzene (mcb).


Chlorobenzene is a sweet-smelling natural compound with the substance recipe C6H5Cl. This dry, combustible fluid is a typical dissolvable and a broadly utilized middle of the road in the production of different synthetic concoctions.


The real utilization of chlorobenzene is as a middle of the road in the generation of items, for example, herbicides, dyestuffs, and elastic. Chlorobenzene is likewise utilized as a high-bubbling dissolvable in numerous mechanical applications just as in the laboratory. Chlorobenzene is nitrated on an expansive scale to give a blend of 2-nitrochlorobenzene and 4-nitrochlorobenzene, which are isolated. These mononitrochlorobenzenes are changed over to related 2-nitrophenol, 2-nitroanisole, bis(2-nitrophenyl)disulfide, and 2-nitroaniline by nucleophilic uprooting of the chloride, with separately sodium hydroxide, sodium methoxide, sodium disulfide, and smelling salts. The transformations of the 4-nitro subsidiary are similar

Chlorobenzene used to be utilized in the assembling of specific pesticides, most outstandingly DDT, by response with chloral (trichloroacetaldehyde), however this application has declined with the reduced utilization of DDT. At one time, chlorobenzene was the fundamental antecedent for the assembling of phenol:

C6H5Cl + NaOH → C6H5OH + NaCl

The response additionally has a side-effect of salt. The response is known as the Dow procedure, with the response did at 350 °C utilizing melded sodium hydroxide without dissolvable. Marking tests demonstrate that the response continues by means of disposal/expansion, through benzyne as the middle of the road.

Creation of mono chloro benzene (mcb)

It was first depicted in 1851. Chlorobenzene is made by chlorination of benzene within the sight of a synergist measure of Lewis corrosive, for example, ferric chloride, sulfur dichloride, and anhydrous aluminum chloride

The impetus upgrades the electrophilicity of the chlorine. Since chlorine is electronegative, C6H5Cl shows to some degree diminished vulnerability to facilitate chlorination. Mechanically the response is led as a nonstop procedure to limit the development of dichlorobenzenes.

Research center courses

Chlorobenzene can be created by from aniline by means of benzenediazonium chloride, the course being known as the Sandmeyer response.


Chlorobenzene shows “low to direct” harmfulness as shown by its LD50 of 2.9 g/kg. The Occupational Safety and Health Administration has set a passable introduction limit at 75 ppm (350 mg/m3) over an eight-hour time-weighted normal for specialists taking care of chlorobenzene.

Toxicology and biodegradation

Chlorobenzene can endure in soil for a while, in air for about 3.5 days, and in water for short of what one day. People might be presented to this specialist by means of breathing tainted air (essentially by means of word related presentation), expending defiled sustenance or water, or by coming into contact with sullied soil (commonly close risky waste destinations). Be that as it may, on the grounds that it has just been found at 97 out of 1,177 NPL dangerous waste destinations, it isn’t viewed as a far reaching ecological contaminant. The bacterium Rhodococcus phenolicus corrupts chlorobenzene as sole carbon sources.

After entering the body, ordinarily through tainted air, chlorobenzene is discharged both by means of the lungs and the urinary framework.

On different planets

In 2015, the SAM science group declared that the Curiosity wanderer detailed proof of higher convergences of chlorobenzene in a sedimentary shake, named “Cumberland”, on Mars.[9] The group conjectured that the chlorobenzene may have been delivered when the example was warmed in the instrument testing chamber. The warming would have set off a response of organics in the Martian soil, which is known to contain perchlorate .

See moreover





NIOSH Pocket Guide to Chemical Hazards. “#0121”. National Institute for Occupational Safety and Health (NIOSH).

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

U. Beck, E. Löser “Chlorinated Benzenes and different Nucleus-Chlorinated Aromatic Hydrocarbons” Ullmann’s Encyclopedia of Industrial Chemistry, 2012, Wiley-VCH, Weinheim. doi:10.1002/14356007.o06_o03

Rossberg, Manfred; Lendle, Wilhelm; Pfleiderer, Gerhard; Tögel, Adolf; Dreher, Eberhard-Ludwig; Langer, Ernst; Rassaerts, Heinz; Kleinschmidt, Peter; Strack, Heinz; Cook, Richard; Beck, Uwe; Lipper, Karl-August; Torkelson, Theodore R.; Löser, Eckhard; Beutel, Klaus K.; Mann, Trevor (2006). “Chlorinated Hydrocarbons”. Ullmann’s Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a06_233.pub2. ISBN 3527306730.

Gerald Booth (2007). “Nitro Compounds, Aromatic”. Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411.

Weber, Manfred; Weber, Markus; Kleine-Boymann, Michael (2004). “Phenol”. Ullmann’s Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a19_299.pub2. ISBN 3527306730.

CDC – NIOSH Pocket Guide to Chemical Hazards

Rehfuss, M.; Urban, J. (2005). “Rhodococcus phenolicus sp. nov., a novel bioprocessor secluded actinomycete with the capacity to corrupt chlorobenzene, dichlorobenzene and phenol as sole carbon sources”. Methodical and Applied Microbiology. 28 (8): 695– 701. doi:10.1016/j.syapm.2005.05.011. PMID 16261859. Mistake: Rehfuss, M. (2006). “Mistake to “Rhodococcus phenolicus sp. nov., a novel bioprocessor separated actinomycete with the capacity to debase chlorobenzene, dichlorobenzene and phenol as sole carbon sources” [Systematic and Applied Microbiology 28 (2005) 695– 701]”. Precise and Applied Microbiology. 29 (2): 182. doi:10.1016/j.syapm.2005.11.005.

Freissinet, C.; et al. (2015). “Natural atoms in the sheepbed mudstone, storm hole, defaces”. Diary of Geophysical Research: Planets. 120 (3): 495– 514. doi:10.1002/2014JE004737.