3,5-Dinitrosalicylic acid

3,5-Dinitrosalicylic acid^[1]
Names
	Preferred IUPAC name 2-Hydroxy-3,5-dinitrobenzoic acid
	Other names 3,5-Dinitrosalicylic acid
Identifiers
CAS Number	609-99-4 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	2220661
ChEBI	CHEBI:53648 ;
ChEMBL	ChEMBL2260697;
ChemSpider	11380 ;
ECHA InfoCard	100.009.278
EC Number	210-204-3;
Gmelin Reference	5309
KEGG	C11319 ;
PubChem CID	11873;
UNII	2ACT5NW8HU ;
CompTox Dashboard (EPA)	DTXSID9060576 ;
	InChI InChI=1S/C7H4N2O7/c10-6-4(7(11)12)1-3(8(13)14)2-5(6)9(15)16/h1-2,10H,(H,11,12) Key: LWFUFLREGJMOIZ-UHFFFAOYSA-N ; InChI=1/C7H4N2O7/c10-6-4(7(11)12)1-3(8(13)14)2-5(6)9(15)16/h1-2,10H,(H,11,12) Key: LWFUFLREGJMOIZ-UHFFFAOYAQ;
	SMILES c1c(cc(c(c1C(=O)O)O)[N+](=O)[O-])[N+](=O)[O-];
Properties
Chemical formula	C7H4N2O7
Molar mass	228.116 g·mol−1
Appearance	Yellow needles or plates
Melting point	182 °C (360 °F; 455 K)
Solubility in water	Soluble
Solubility in organic solvents	Soluble in ethanol, diethyl ether, benzene
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H315, H318, H319, H335
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
	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

3,5-Dinitrosalicylic acid (DNS or DNSA, IUPAC name 2-hydroxy-3,5-dinitrobenzoic acid) is an aromatic compound that reacts with reducing sugars and other reducing molecules to form 3-amino-5-nitrosalicylic acid, which strongly absorbs light at 540 nm. It was first introduced as a method to detect reducing substances in urine by James B. Sumner^[2] and has since been widely used, for example, for quantifying carbohydrate levels in blood.^[3] It is mainly used in assay of alpha-amylase. However, enzymatic methods are usually preferred due to DNS's lack of specificity.^[4]

Synthesis edit

3,5-Dinitrosalicylic acid can be prepared by the nitration of salicylic acid.^[5]

References edit

^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 3–318. ISBN 978-0-8493-0594-8.
^ Sumner, J.B. Dinitrosalicylic acid: a reagent for the estimation of sugar in normal and diabetic urine. Journal of Biological Chemistry 47, 5, 1921.
^ "Description of lab use from the Department of Chemical Engineering, University of Maryland". Archived from the original on 2007-08-17. Retrieved 2006-03-17.
^ Miller, Gail Lorenz (1959). "Use of dinitrosalicylic acid reagent for determination of reducing sugar". Anal. Chem. 31 (3): 426–428. doi:10.1021/ac60147a030.
^ Thiel, W.; Mayer, R.; Jauer, E.-A.; Modrow, H.; Dost, H.: Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series in J. Prakt. Chem. (Leipzig) 328 (1986) 497-514, doi:10.1002/prac.19863280406.

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[hand-1] Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 3–318. ISBN 978-0-8493-0594-8.

[2] Sumner, J.B. Dinitrosalicylic acid: a reagent for the estimation of sugar in normal and diabetic urine. Journal of Biological Chemistry 47, 5, 1921.

[3] "Description of lab use from the Department of Chemical Engineering, University of Maryland". Archived from the original on 2007-08-17. Retrieved 2006-03-17.

[4] Miller, Gail Lorenz (1959). "Use of dinitrosalicylic acid reagent for determination of reducing sugar". Anal. Chem. 31 (3): 426–428. doi:10.1021/ac60147a030.

[Thiel-5] Thiel, W.; Mayer, R.; Jauer, E.-A.; Modrow, H.; Dost, H.: Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series in J. Prakt. Chem. (Leipzig) 328 (1986) 497-514, doi:10.1002/prac.19863280406.

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