3-Nitrobenzoic acid, 99%, Thermo Scientific Chemicals
3-Nitrobenzoic acid, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Nitrobenzoic acid, 99%, Thermo Scientific Chemicals

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Catalog number A13494.30
also known as A13494-30
Price (USD)/ Each
36.30
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Quantity:
250 g
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Price (USD)/ Each
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3-Nitrobenzoic acid, 99%, Thermo Scientific Chemicals
Catalog numberA13494.30
Price (USD)/ Each
36.30
-
Add to cart
Chemical Identifiers
CAS121-92-6
IUPAC Name3-nitrobenzoic acid
Molecular FormulaC7H5NO4
InChI KeyAFPHTEQTJZKQAQ-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=CC(=C1)[N+]([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream or pale yellow
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Melting Point139.5-145.5?C
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
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3-Nitrobenzoic acid was used to investigated the role of ozone as additional decomposition or finishing reagent in the degradation of o-, m- and p-nitobenzoic acids

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
3-Nitrobenzoic acid was used to investigated the role of ozone as additional decomposition or finishing reagent in the degradation of o-, m- and p-nitobenzoic acids

Solubility
Soluble in water. Insoluble in acetic acid.

Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Narender P. Luthra.; R.Bruce Dunlap.; Jerome D. Odom. Characterization of a new sulfhydryl group reagent: 6,6'-Diselenobis-(3-Nitrobenzoic acid), a selenium analog of Ellman's reagent. Analytical Biochemistry. 1981, 117, (1), 94-102.
  2. Henrik Stephensen.; Florencio Zaragoza. Solid-phase synthesis of N-hydroxyindoles and benzo[c]isoxazoles by C-arylation of substituted acetonitriles and 1,3-dicarbonyl compounds with polystyrene-bound aryl fluorides. Tetrahedron Letters. 1999, 40, (31), 5799-5802.