ANTHRANILIC ACID
| Anthranilic Acid | ||
|---|---|---|
| General | ||
| Systematic name | 2-aminobenzoic acid | |
| Other names | vitamin L1, Anthranilate | |
| Molecular formula | C7H7NO2 | |
| Molar mass | 137.136 g/mol | |
| CAS number | [118-92-3] | |
| Properties | ||
| Solubility in water | 0.6 g/L | |
| Solubility in | Hot water | |
| Density | 1.4 g/cm3 | |
| Melting point (m.p.) | 146-148 °C | |
| Boiling point | Sublimes]] above m.p.IPCS | |
| Hazards | ||
| MSDS | External (html) | |
| EU classification | ||
| R-phrases | ||
| S-phrases | ||
| Flash point | >150 °C | |
| LD50 oral, mouse | 1400 mg/kg | |
| LD50 oral, rat | 5410 mg/kg. | |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | ||
'Anthranilic acid' is the organic compound with the formula C6H4(NH2)CO2H. This amino acid is white solid when pure, although commercial samples may appear yellow. The molecule consists of a benzene ring with two adjacent funcitonal groups, a carboxylic acid and an amine. Because these two groups are polar, this organic compound is highly soluble in water. It is sometimes referred to as vitamin L
Anthranilic acid is biosynthesized from chorismic acid. It is the precursor to the amino acid tryptophan via the attachment of a ribose to the amine group.
| Contents |
| Uses |
| See also |
| References |
| External links |
Uses
Anthranilic acid is used as an intermediate for production of dyes, pigments, and saccharin. It and its esters are used in preparing perfumes, pharmaceuticals and UV-absorber as well as corrosion inhibitors for metals and mold inhibitors in soya sauce.
Anthranilic acid can be used in organic synthesis to generate the benzyne intermediate.[1]
See also
★ Kynureninase
References
1. Logullo, F. M.; Seitz, A. H.; Friedman, L. "Benzenediazonium-2-carboxy- and Biphenylene" Organic Syntheses, Collected Volume 5, p.54 (1973).http://www.orgsyn.org/orgsyn/pdfs/CV5P0054.pdf
External links
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