1,4-Dinitrobenzene, 98+%
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1,4-Dinitrobenzene, 98+%
1,4-Dinitrobenzene, 98+%
1,4-Dinitrobenzene, 98+%
Thermo Scientific Chemicals

1,4-Dinitrobenzene, 98+%

CAS: 100-25-4 | C6H4N2O4 | 168.108 g/mol
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Catalog number A10293.22
also known as A10293-22
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Chemical Identifiers
CAS100-25-4
IUPAC Name1,4-dinitrobenzene
Molecular FormulaC6H4N2O4
InChI KeyFYFDQJRXFWGIBS-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC=C(C=C1)[N+]([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Pale yellow or orange to brown
FormPowder or crystalline powder or crystals and/or chunks
Assay (GC)≥98%
Identification (FTIR)Conforms
1,4-Dinitrobenzene is used in a study to evaluate the ionization mechanism and solvent effect by novel atmospheric pressure photoionization mass spectrometry in negative ion mode for analysis of some compounds. 1,4-Dinitrobenzene can be used in synthesis of dyes and dye intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,4-Dinitrobenzene is used in a study to evaluate the ionization mechanism and solvent effect by novel atmospheric pressure photoionization mass spectrometry in negative ion mode for analysis of some compounds. 1,4-Dinitrobenzene can be used in synthesis of dyes and dye intermediates.

Solubility
Soluble in water. (0.8 g/L) at 20°C.

Notes
Incompatible with bases, alkali metals, oxidizing agents and nitric acid.
RUO – Research Use Only

General References:

  1. Tiina J Kauppila; Tapio Kotiaho; Risto Kostiainen; Andries P Bruins. Negative ion-atmospheric pressure photoionization-mass spectrometry. Journal of the American Society for Mass Spectrometry. 2004, 15 (2), 203-211.
  2. Hui Li; Brian J Teppen; Cliff T Johnston; Stephen A Boyd. Thermodynamics of nitroaromatic compound adsorption from water by smectite clay. Environmental Science & Technology. 2004, 38 (20), 5433-5442.
  3. Displacement of one activated nitro-group by phenoxides has been used as a route to hindered diaryl ethers: J. Chem. Soc., Perkin 1, 3229 (1988):