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| 3-Nitrobenzoic acid Basic information |
| 3-Nitrobenzoic acid Chemical Properties |
| Melting point | 139-141 °C(lit.) | | Boiling point | 295.67°C (rough estimate) | | density | 1,494 g/cm3 | | vapor density | 5.76 (vs air) | | vapor pressure | 0.005Pa at 25℃ | | refractive index | 1.6280 (estimate) | | Fp | 190 °C | | storage temp. | no restrictions. | | solubility | water: soluble3g/L at 25°C | | form | Crystals or Powder | | pka | 3.47(at 25℃) | | color | Slightly green to light yellow | | PH | 3 (5g/l, H2O, 20℃)(aqueous suspension) | | PH Range | 3 | | Water Solubility | <0.01 g/100 mL at 18 ºC | | Merck | 14,6588 | | BRN | 908644 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | InChIKey | AFPHTEQTJZKQAQ-UHFFFAOYSA-N | | LogP | 1.1 at 25℃ | | CAS DataBase Reference | 121-92-6(CAS DataBase Reference) | | NIST Chemistry Reference | Benzoic acid, 3-nitro-(121-92-6) | | EPA Substance Registry System | m-Nitrobenzoic acid (121-92-6) |
| 3-Nitrobenzoic acid Usage And Synthesis |
| Chemical Properties | White or light yellow monoclinic leaf-like crystal. Soluble in acetone, chloroform, ethanol and ether, slightly soluble in benzene, water, carbon disulfide and petroleum ether, more soluble in hot water. It smells like almonds. 3-nitrobenzoic acid is quite a strong acid, it is soluble in a relatively weak base. It is about ten times more acidic than benzoic acid.The conjugate base of benzoic acid is stabilised by the presence of the electron withdrawing nitro group which explains its increased acidity in comparison to unsubstituted benzoic acid. | | Uses | 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 | | Application | 3-Nitrobenzoic acid is an intermediate of photosensitive materials, functional pigments and drugs. In the pharmaceutical industry, it is used to produce bile acid, acetic acid and so on.m-nitrobenzoic acid is a reagent used in the coupling of allyl acetate to allylic, aliphatic and benzylic alcohols. It is also used as a chemoattractant against Pseudomonas strains. | | Preparation | 3-Nitrobenzoic acid is prepared by nitrating benzoic acid at low temperature. Approximately 20% of the 2-nitro isomer and 1.5% of the 4-nitro isomer are co-produced. The 3-nitrobenzoic acid can be purified by recrystallization of the sodium salt. The oxidation of 3-nitrobenzaldehyde, prepared by the controlled oxidation of benzaldehyde, gives a higher yield. | | Synthesis Reference(s) | Organic Syntheses, Coll. Vol. 1, p. 391, 1941The Journal of Organic Chemistry, 46, p. 3056, 1981 DOI: 10.1021/jo00328a013 | | General Description | Off white to yellowish-white crystals. Bitter taste. Melts in hot water. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | 3-Nitrobenzoic acid is incompatible with strong oxidizers. 3-Nitrobenzoic acid is also incompatible with strong bases. 3-Nitrobenzoic acid may react with cyanides. | | Fire Hazard | Flash point data for 3-Nitrobenzoic acid are not available but 3-Nitrobenzoic acid is probably combustible. | | Flammability and Explosibility | Nonflammable | | Purification Methods | Crystallise the acid from *benzene, H2O, EtOH (charcoal), glacial acetic acid or MeOH/H2O. Dry and store it in a vacuum desiccator. The amide has m 143o (from H2O or *C6H6). [Beilstein 9 III 1489, 9 IV 1055.] |
| 3-Nitrobenzoic acid Preparation Products And Raw materials |
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