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M dinitrobenzene

Manufactured by Merck Group
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Sourced in China

M-dinitrobenzene is a chemical compound used as a laboratory reagent. It is a crystalline solid with a yellow color. M-dinitrobenzene has applications in organic synthesis and can be used as a precursor for other chemical compounds.

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Lab products found in correlation

Dehydroascorbic acid, by Merck Group (1 mentions) Ch3cn, by Merck Group (1 mentions) 4 nitrophenol, by Merck Group (1 mentions) 3 5 dinitrobenzoic acid, by Merck Group (1 mentions) 4 nitrobenzoic acid, by Merck Group (1 mentions) Ascorbic acid, by Merck Group (1 mentions) 2 naphthol, by Merck Group (1 mentions) 1 naphthylamine, by Merck Group (1 mentions) O dichlorobenzene, by J&K Scientific (1 mentions) 1 3 5 trimethylbenzene, by Maclin Biochemical Technology (1 mentions) M xylene, by Merck Group (1 mentions) P xylene, by Merck Group (1 mentions) Naphthalene, by Merck Group (1 mentions) Toluene, by Nanjing Chemical Reagent (1 mentions) Phenanthrene, by Merck Group (1 mentions)

2 protocols using m dinitrobenzene

1

Pyrene-based Luminescent Probe Synthesis

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1-Pyrenecarboxaldehyde,
4-nitrochlorobenzene,
ethylenediamine (Sigma-Aldrich), absolute ethanol, salts of cations
like Ca2+, Al3+, Co2+, Cd2+, Cr3+, Fe3+, Cu2+, K+, Mn2+, Mg2+, Na+, Ni2+, Zn2+, and Pb2+ and different reactive molecules/ions
like •OH, H2O2, NO3–, O2–, ClO–, (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) radical, NO2–, ONOO–, ascorbic acid
(AA), dehydroascorbic acid (DHA), and DEA-NONOate as well as 2,4,6-trinitrophenol
(TNP), 2,4-dinitrophenol (DNP), 4-nitrophenol (4-NP), p-choloronitrobenzene (Cl-NB), m-dinitrobenzene (DNB),
3,5-dinitrobenzoic acid (DNBA), and 4-nitrobenzoic acid (4-NBA) were
obtained from commercial suppliers and Sigma-Aldrich, which were used
without further purification. The reagent-grade solvents like CH3CN (Merck, India), MeOH, and tetrahydrofuran were dried before
use.
Islam A.S., Sasmal M., Maiti D., Dutta A., Show B, & Ali M. (2018). Design of a Pyrene Scaffold Multifunctional Material: Real-Time Turn-On Chemosensor for Nitric Oxide, AIEE Behavior, and Detection of TNP Explosive. ACS Omega, 3(8), 10306-10316.
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2

Characterization of Aromatic Compounds and Graphene Derivatives

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The aromatic compounds used in this study included benzene (99.5%; Shanghai Lingfeng Chemical Reagent Co. Ltd., China), naphthalene (99%; Sigma-Aldrich), phenanthrene (98%; Sigma-Aldrich), 1-naphthylamine (98%; Sigma-Aldrich), 2-naphthol (99%; Sigma-Aldrich), chlorobenzene (99.0%; Shanghai Lingfeng Chemical Reagent Co. Ltd.), o-dichlorobenzene (99%; J&K Chemical, China), m-dichlorobenzene (97%; Sigma-Aldrich), p-dichlorobenzene (99.5%; Fluka, Switzerland), 1,2,4-trichlorobenzene (99.0%; Fluka), 1,3,5-trichlorobenzene (99%; Supelco, USA), p-chlorophenol (99%; Alfa Aesar, USA), p-chloroaniline (98%; Nanjing Chemical Reagent Co. Ltd., China), toluene (99.5%; Nanjing Chemical Reagent Co. Ltd), o-xylene (98.0%; Supelco), m-xylene (99.5%; Sigma-Aldrich), p-xylene (99.5%; Sigma-Aldrich), 1,3,5-trimethylbenzene (97%; Macklin, China), nitrobenzene (99.5%; Fluka), m-dinitrobenzene (97%; Sigma-Aldrich), and 1,3,5-trinitrobenzene (99.9%; Sigma-Aldrich). GO (99.0%) and RGO (98.9%) were purchased from XFNANO Materials Tech (China). GO was prepared by the modified Hammers method (18 (link), 23 ) and was mainly in the form of nanosheets with a diameter of 0.5 to 5 μm and thickness of 0.8 to 1.2 nm (according to the information provided by the manufacturer). RGO was prepared by the reduction of GO using l-ascorbic acid (48 ). All these materials were used without further purification.
Fu H., Wang B., Zhu D., Zhou Z., Bao S., Qu X., Guo Y., Ling L., Zheng S., Duan P., Mao J., Schmidt-Rohr K., Tao S, & Alvarez P.J. (2022). Mechanism for selective binding of aromatic compounds on oxygen-rich graphene nanosheets based on molecule size/polarity matching. Science Advances, 8(30), eabn4650.
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