| Weight | 228.116 g/mol |
|---|---|
| Formula | C7H4N2O7 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
3,5-DINITROSALICYLIC ACID (609-99-4)
3,5-dinitrosalicylic acid, monorubidium salt · 3,5-dinitrosalicylic acid, monopotassium salt · 3,5-dinitrosalicylic acid, monolithium salt
Score:
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- Solubilities ofo-acetylsalicylic, 4-aminosalicylic, 3,5-dinitrosalicylic, andp-toluic acid, and magnesium-DL-aspartate in water fromT=(278 to 348) K (The Journal of Chemical Thermodynamics, 1999)
- Comparison of the 3,5-dinitrosalicylic acid and NelsonSomogyi methods of assaying for reducing sugars and determining cellulase activity (Enzyme and Microbial Technology, 1985)
- A colorimetric estimation of reducing sugars in potatoes with 3,5-dinitrosalicylic acid (Potato Research, 1973)
- Molecular cocrystals of carboxylic acids. XX. The crystal structures of 3, 5-Dinitrosalicylic acid and its adducts with the isomeric monoaminobenzoic acids (Australian Journal of Chemistry, 1995)
- Synthesis, spectroscopic investigations, antimicrobial and DNA binding studies of a new charge transfer complex of o-phenylenediamine with 3,5-dinitrosalicylic acid (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2013)
- Amino acids interference on the quantification of reducing sugars by the 3,5-dinitrosalicylic acid assay mislead carbohydrase activity measurements (Carbohydrate Research, 2012)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5-dinitrosalicylic acid, monorubidium salt
- 3,5-dinitrosalicylic acid, monopotassium salt
- 3,5-dinitrosalicylic acid, monolithium salt
- 3,5-dinitrosalicylic acid, monosodium salt
- 3,5-dinitrosalicylic acid, dipotassium salt
- 3,5-dinitrosalicylic acid, dilithium salt
- 3,5-dinitrosalicylic acid, monocesium salt
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SMILESC1=C(C=C(C(=C1[N+](=O)[O-])O)C(=O)O)[N+](=O)[O-]
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InChIKeyLWFUFLREGJMOIZ-UHFFFAOYSA-N
- Pubchem - 3,5-DINITROSALICYLIC ACID
- Wikipedia - 3,5-dinitrosalicylic acid
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 and has since been widely used, for example, for quantifying carbohydrate levels in blood. It is mainly used in assay of alpha-amylase.
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3,5-DINITROSALICYLIC ACID
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