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2-Nitrobenzoic acid, 95%
CAS: 552-16-9 | C7H5NO4 | 167.12 g/mol
| Catalog Number | Quantity |
|---|---|
| ALFA10393.22 | 100 g |
Catalog number ALFA10393.22
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Quantity:
100 g
Specifications
Chemical Name or Material2-Nitrobenzoic acid
CAS552-16-9
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H341-H315-H319-H335
Suspected of causing genetic defects.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H341-H315-H319-H335
Suspected of causing genetic defects.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
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It is employed as a synthetic reagent and can function as a growth supplement for Pseudomonas fluorescens strain KU-7. It also finds its use as a reagent for protection of amine groups and in organic synthesis.
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
It is employed as a synthetic reagent and can function as a growth supplement for Pseudomonas fluorescens strain KU-7. It also finds its use as a reagent for protection of amine groups and in organic synthesis.
Solubility
Soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
It is employed as a synthetic reagent and can function as a growth supplement for Pseudomonas fluorescens strain KU-7. It also finds its use as a reagent for protection of amine groups and in organic synthesis.
Solubility
Soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Y Hasegawa, et al. A novel degradative pathway of 2-nitrobenzoate via 3-hydroxyanthranilate in Pseudomonas fluorescens strain KU-7.FEMS Microbiol Lett.,2000,190(2), 185-190.
- Smith, G, et al. Molecular adducts of 2,6-diaminopyridine with nitro-substituted aromatic carboxylic acids and the crystal structure of the 1:1 adduct of 2,6-diaminopyridine with 2-nitrobenzoic acid.Australian Journal of Chemistry.,1999,52(1), 71-74.