N-Ethyl-N-hydroxyethylaniline

N-Ethyl-N-hydroxyethylaniline
  • CAS No.:92-50-2
Other grades of this product :
N-Ethyl-N-hydroxyethylaniline Basic information
Product Name:N-Ethyl-N-hydroxyethylaniline
Synonyms:2-(Ethylanilino)ethanol;2-(ethylphenylamino)-ethano;2-(N-Ethyl-N-phenylamino)ethanol;N-ETHYL-N-PHENYLETHANOLAMINE;N-(B-HYDROXYETHYL)-N-ETHYLANILINE;N-Ethyl-N-hydroxyethylaniline, 96% 100GR;2-[Phenyl(ethyl)amino]ethanol;N-Ethyl-N-hydroxyethylaniline,96%
CAS:92-50-2
MF:C10H15NO
MW:165.23
EINECS:202-160-9
Product Categories:aniline derivatives;Amino Alcohols;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Intermediates of Dyes and Pigments;Amino Alcohols;Organic Building Blocks;Oxygen Compounds;organic chemical
Mol File:92-50-2.mol
N-Ethyl-N-hydroxyethylaniline Chemical Properties
Melting point 36-38 °C (lit.)
Boiling point 268 °C (lit.)
density 1.02
vapor pressure 1Pa at 25℃
refractive index 1.5605-1.5625
Fp 120 °C
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Liquid
pka14.66±0.10(Predicted)
color Clear colorless to yellow to orange, product may darken in storage
Water Solubility 4.975g/L(20 ºC)
InChIKeyHYVGFUIWHXLVNV-UHFFFAOYSA-N
LogP1.88 at 20℃
CAS DataBase Reference92-50-2(CAS DataBase Reference)
NIST Chemistry ReferenceEthanol, 2-(ethylphenylamino)-(92-50-2)
EPA Substance Registry SystemEthanol, 2-(ethylphenylamino)- (92-50-2)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38-36
Safety Statements 36/37/39-39-26
WGK Germany 2
RTECS KL0878000
HS Code 29221990
MSDS Information
ProviderLanguage
2-(N-Ethylanilino)ethanol English
SigmaAldrich English
ACROS English
N-Ethyl-N-hydroxyethylaniline Usage And Synthesis
Chemical Propertiesclear yellow liquid after melting
Uses2-(N-Ethylanilino) ethanol was used in the preparation of azo compound N-ethyl-N-(2-hydroxylethyl)-4-(2-cyano-4-nitrophenylazo) aniline (AZ1)2.
General Description2-(N-Ethylanilino) ethanol couples with 2-amino-5-formylthiophene during the synthesis of nonlinear optical chromophores. It undergoes azo coupling with 2-cyan-4-nitroaniline to yield azochromophore AZ1.

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