4-Nitrobenzoic acid

4-Nitrobenzoic acid
Names
	Preferred IUPAC name 4-Nitrobenzoic acid
	Other names p-Nitrobenzoic acid
Identifiers
CAS Number	62-23-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:262350 ;
ChEMBL	ChEMBL101263 ;
ChemSpider	5882 ;
ECHA InfoCard	100.000.479
PubChem CID	6108;
UNII	G83NWR61OW ;
CompTox Dashboard (EPA)	DTXSID3020966 ;
	InChI InChI=1S/C7H5NO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4H,(H,9,10) Key: OTLNPYWUJOZPPA-UHFFFAOYSA-N ; InChI=1/C7H5NO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4H,(H,9,10) Key: OTLNPYWUJOZPPA-UHFFFAOYAB;
	SMILES O=[N+]([O-])c1ccc(C(=O)O)cc1;
Properties
Chemical formula	C7H5NO4
Molar mass	167.1189 g/mol
Appearance	Light yellow crystalline powder
Density	1.58
Melting point	237 °C (459 °F; 510 K)
Boiling point	Sublimes
Solubility in water	<0.1 g/100 mL at 26 °C
Acidity (pKa)	3.41 (in water), 9.1 (in DMSO)
Magnetic susceptibility (χ)	-78.81·10−6 cm3/mol
Related compounds
Related compounds	Benzoic acid; Nitrobenzene; Anthranilic acid; 3,5-Dinitrobenzoic acid, 3-Nitrobenzoic acid, 2-Nitrobenzoic acid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

4-Nitrobenzoic acid is an organic compound with the formula C₆H₄(NO₂)CO₂H. It is a pale yellow solid. It is a precursor to 4-nitrobenzoyl chloride, the precursor to the anesthetic procaine and folic acid. It is also a precursor to 4-aminobenzoic acid.^[6]

Production

4-Nitrobenzoic acid is prepared by oxidation of 4-nitrotoluene using oxygen or dichromate as oxidants.^[7]

Alternatively, it has been prepared by nitration of polystyrene followed by oxidation of the alkyl substituent. This method proceeds with improved para/ortho selectivity owing to the steric protection of the ortho positions by the polymer backbone.

Safety

This compound has a rat LD₅₀ of 1960 mg/kg.^[8]

References

^ "4-nitrobenzoic acid - PubChem Public Chemical Database". Retrieved 11 April 2010.
^ ^a ^b ^c ^d "Safety data for p-nitrobenzoic acid". Archived from the original on 27 May 2008. Retrieved 11 April 2010.
^ "p-Nitrobenzoic acid". Archived from the original on 7 May 2010. Retrieved 11 April 2010.
^ "Dissociation Constants Of Organic Acids And Bases". Retrieved 11 April 2010.
^ "Bordwell pKa Table (Acidity in DMSO)". Retrieved 11 April 2010.
^ Takao Maki; Kazuo Takeda (2002). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_555. ISBN 3527306730..
^ O. Kamm; A. O. Matthews (1922). "p-Nitrobenzoic Acid". Org. Synth. 2: 53. doi:10.15227/orgsyn.002.0053.
^ "Material Safety Data Sheet - P-nitrobenzoic acid MSDS". Archived from the original on 7 August 2011. Retrieved 11 April 2010.

[pubchem-1] "4-nitrobenzoic acid - PubChem Public Chemical Database". Retrieved 11 April 2010.

[msds.chem.ox.ac.uk-2] "Safety data for p-nitrobenzoic acid". Archived from the original on 27 May 2008. Retrieved 11 April 2010.

[chemicalbook-3] "p-Nitrobenzoic acid". Archived from the original on 7 May 2010. Retrieved 11 April 2010.

[pkaValues-4] "Dissociation Constants Of Organic Acids And Bases". Retrieved 11 April 2010.

[bordwell-5] "Bordwell pKa Table (Acidity in DMSO)". Retrieved 11 April 2010.

[6] Takao Maki; Kazuo Takeda (2002). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_555. ISBN 3527306730..

[7] O. Kamm; A. O. Matthews (1922). "p-Nitrobenzoic Acid". Org. Synth. 2: 53. doi:10.15227/orgsyn.002.0053.

[scienceLab-8] "Material Safety Data Sheet - P-nitrobenzoic acid MSDS". Archived from the original on 7 August 2011. Retrieved 11 April 2010.

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