Date published: 2026-5-20

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3,5-Dinitrosalicylaldehyde (CAS 2460-59-5)

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CAS Number:
2460-59-5
Molecular Weight:
212.12
Molecular Formula:
(O2N)2C6H2-2-(OH)CHO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3,5-Dinitrosalicylaldehyde (DNSA) is a highly versatile and widely employed reagent in both organic and biochemistry laboratories. This compound exists as yellow to orange-red crystalline solids and exhibits excellent solubility in water, alcohols, and various organic solvents. The extensive utilization of 3,5-Dinitrosalicylaldehyde in scientific research is attributed to its broad reactivity with various molecules. It serves as a valuable labeling agent for proteins, carbohydrates, and lipids. Moreover, 3,5-Dinitrosalicylaldehyde finds application in detecting and quantifying the concentration of specific molecules, such as glucose and cholesterol, in biological samples. Furthermore, this compound facilitates the identification of certain enzymes, including proteases and glycosidases, in biological samples. The reactivity of 3,5-Dinitrosalicylaldehyde arises from a process known as Schiff-base formation. This involves the reaction between a carbonyl group on the 3,5-Dinitrosalicylaldehyde molecule and a primary amine group on the target molecule. Through this reaction, a covalent bond is formed between the two molecules, enabling 3,5-Dinitrosalicylaldehyde to serve as a reliable label for the target molecule.


3,5-Dinitrosalicylaldehyde (CAS 2460-59-5) References

  1. Preparation of general proteinase substrates using 3,5-dinitrosalicylaldehyde.  |  Gallegos, NG., et al. 1996. J Biochem Biophys Methods. 33: 31-41. PMID: 8905466
  2. Chiral Ru(II) Schiff base complex-catalysed enantioselective epoxidation of styrene derivatives using iodosyl benzene as oxidant. II  |  R.I Kureshy, N.H Khan, S.H.R Abdi, S.T Patel, P Iyer. 1999. Journal of Molecular Catalysis A: Chemical. 150: 175-183.
  3. Synthesis, physico-chemical studies and solvent-dependent enantioselective epoxidation of 1,2-dihydronaphthalene catalysed by chiral Ruthenium(II) Schiff base complexes. I  |  R.I Kureshy, N.H Khan, S.H.R Abdi, S.T Patel, P Iyer. 1999. Journal of Molecular Catalysis A: Chemical. 150: 163-173.
  4. Dynamic Kinetic Resolution of α-Amino Acid Esters in the Presence of Aldehydes  |  Daniel A. Schichl, Stephan Enthaler, Wolfgang Holla, Thomas Riermeier, Udo Kragl, Matthias Beller. 2008. European Journal of Organic Chemistry. 2008: 3506-3512.
  5. Catalytic activity of Schiff base cobalt(III) complexes immobilized on terpolymers of glycidyl methacrylate in the addition of carboxylic acids to terminal epoxides  |  Agnieszka Bukowska, Wiktor Bukowski, Jarosław Noworól. 2010. 117: 655-663.
  6. Fluorescein hydrazone-based supramolecular architectures, molecular recognition, sequential logic operation and cell imaging  |  Kamini Tripathi a, Abhishek Rai a, Amarish Kumar Yadav b, Saripella Srikrishna b, Niraj Kumari *a and Lallan Mishra *a. 2017. RSC Adv. 7: 2264-2272.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3,5-Dinitrosalicylaldehyde, 1 g

sc-226318
1 g
$57.00