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| 2-Anilinoethanol Basic information |
| 2-Anilinoethanol Chemical Properties |
Melting point | -30 °C | Boiling point | 150-152 °C10 mm Hg(lit.) | density | 1.094 g/mL at 25 °C(lit.) | vapor density | >1 (vs air) | vapor pressure | <0.01 mm Hg ( 20 °C) | refractive index | n20/D 1.578(lit.) | Fp | >230 °F | storage temp. | Store below +30°C. | solubility | 4.5g/l | pka | 14.39±0.10(Predicted) | form | clear liquid | color | Colorless to Red to Green | PH | 10.2 (10g/l, H2O, 20℃) | explosive limit | 1-6.8%(V) | Water Solubility | 53 g/L (20 ºC) | BRN | 774672 | InChIKey | MWGATWIBSKHFMR-UHFFFAOYSA-N | LogP | 0.9 at 23℃ | CAS DataBase Reference | 122-98-5(CAS DataBase Reference) | NIST Chemistry Reference | Ethanol, 2-(phenylamino)-(122-98-5) | EPA Substance Registry System | Ethanol, 2-(phenylamino)- (122-98-5) |
| 2-Anilinoethanol Usage And Synthesis |
Chemical Properties | CLEAR YELLOW TO BROWN LIQUID | Uses | N-Phenylethanolamine is used as an intermediate for dyes and other organic compounds. Further, it is used as a substrate for human olfactory uridine 5'-diphospho-glucuronosyltransferase. | Uses | N-(2-Hydroxyethyl)aniline was employed as substrate for human olfactory UDP-glucuronosyltransferase. | Definition | ChEBI: 2-Anilinoethanol is an aralkylamine. | Synthesis Reference(s) | Journal of Medicinal Chemistry, 11, p. 87, 1968 DOI: 10.1021/jm00307a019 Journal of the American Chemical Society, 74, p. 5514, 1952 Tetrahedron Letters, 10, p. 4555, 1969 DOI: 10.1017/S0009838800024678 | Synthesis Reference(s) | Synthetic Communications, 24, p. 1415, 1994 DOI: 10.1080/00397919408011745 | Flammability and Explosibility | Notclassified | Safety Profile | Poison by skin contact,
intraperitoneal, and intravenous routes.
Moderately toxic by ingestion. A skin and
severe eye irritant. Combustible when
exposed to heat or flame. To fight fire, use
dry chemical, water mist. When heated to
decomposition it emits toxic fumes of NOx. |
| 2-Anilinoethanol Preparation Products And Raw materials |
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