N-Phenylglycine
N-Phenylglycine is an organic compound with the formula C6H5NHCH2CO2H. This white solid achieved fame as the industrial precursor to indigo dye.[1] It is a non-proteinogenic alpha amino acid related to sarcosine, but with an N-phenyl group in place of N-methyl.
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| Names | |
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| IUPAC name
2-Anilinoacetic acid | |
| Other names
Anilinoacetic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.002.792 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C8H9NO2 | |
| Molar mass | 151.165 g·mol−1 |
| Appearance | white solid |
| Melting point | 127–128 °C (261–262 °F; 400–401 K) |
| Hazards | |
| GHS pictograms |  |
| GHS Signal word | Warning |
GHS hazard statements |
H315, H319, H335 |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Preparation
It is prepared by the Strecker reaction involving the reaction of formaldehyde, hydrogen cyanide, and aniline. The resulting amino nitrile is hydrolyzed to give the carboxylic acid.[2]
Pfleger's historic synthesis of indigo using N-phenylglycine
gollark: Was there a release?
gollark: * possible release
gollark: What do you have up, anyway, sunfish?
gollark: The forum: hive of scum and villainy.
gollark: Look, they were good eggs!
See also
- Phenylglycine, an isomer with the formula C6H5CH(NH2)CO2H.
References
- Helmut Schmidt (1997). "Indigo – 100 Jahre industrielle Synthese". Chemie in Unserer Zeit. 31 (3): 121–128. doi:10.1002/ciuz.19970310304.
- Elmar Steingruber "Indigo and Indigo Colorants" Ullmann's Encyclopedia of Industrial Chemistry 2004, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a14_149.pub2
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