N-Phenylethanolamine, 98%, Thermo Scientific Chemicals
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N-Phenylethanolamine, 98%, Thermo Scientific Chemicals
N-Phenylethanolamine, 98%, Thermo Scientific Chemicals
N-Phenylethanolamine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

N-Phenylethanolamine, 98%, Thermo Scientific Chemicals

CAS: 122-98-5 | C8H11NO | 137.182 g/mol
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Catalog NumberQuantity
ALFB22131.36500 g
Catalog number ALFB22131.36
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Quantity:
500 g
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Chemical Identifiers
CAS74470-23-8
IUPAC Name2-(methylsulfanyl)pyridine-3-carboxylate
Molecular FormulaC7H6NO2S
InChI KeyCOPSJQVPEUUOKY-UHFFFAOYSA-M
SMILESCSC1=NC=CC=C1C([O-])=O
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SpecificationsSpecification SheetSpecification Sheet
Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
Melting Point (clear melt)213.5-219.5?C
Appearance (Color)White
Assay (Silylated GC)≥98.0%
FormCrystals or powder or crystalline powder
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.

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
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.

Solubility
Slightly miscible with water.

Notes
Incompatible with acids, acid anhydrides, acid chlorides and chloroformates.
RUO – Research Use Only

General References:

  1. Wei, X.; Wan, S.; Jiang, X.; Wang, Z.; Gao, S. Peanut-Shell-like Porous Carbon from Nitrogen-Containing Poly-N-phenylethanolamine for High-Performance Supercapacitor. ACS Appl. Mater. Interfaces 2015, 7 (40), 22238-22245.
  2. Li, C.; Liu, Y.; Zhang, Y.; Zhang, X. An approach to the anticoagulant agent rivaroxaban via an isocyanate-oxirane cycloaddition promoted by MgI2.etherate. J. Chem. Res. 2011, 35 (7), 400-401.
  3. Stanicki, D.; Pottier, M.; Gantois, N.; Pinçon, C.; Forge, D.; Mahieu, I.; Boutry, S.; Eynde, J. J. V.; Martinez, A.; Dei-Cas, E.; Aliouat, E. M. Diamidines versus Monoamidines as Anti-Pneumocystis Agents: An in Vivo Study. Pharmaceuticals 2013, 6 (7), 837-850.