102091
3-Diethylaminophenol
97%
Synonym(s):
3-(Diethylamino)phenol, m-(Diethylamino)phenol
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About This Item
Linear Formula:
(C2H5)2NC6H4OH
CAS Number:
Molecular Weight:
165.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-090-9
Beilstein/REAXYS Number:
908212
MDL number:
Assay:
97%
Form:
solid
InChI key
WAVOOWVINKGEHS-UHFFFAOYSA-N
InChI
1S/C10H15NO/c1-3-11(4-2)9-6-5-7-10(12)8-9/h5-8,12H,3-4H2,1-2H3
SMILES string
CCN(CC)c1cccc(O)c1
assay
97%
form
solid
bp
170 °C/15 mmHg (lit.)
Quality Level
functional group
amine
Related Categories
General description
3-Diethylaminophenol is raw material required for the synthesis of Rhodamine derivatives.
Application
3-Diethylaminophenol was used as starting reagent for the synthesis of silyloxyaniline. It was used in the synthesis of Nile Red and its hydroxy-derivative.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
285.8 °F
flash_point_c
141 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Photoconductive Nile red cyclopalladated metallomesogens.
Ionescu A, et al.
Journal of Materials Chemistry, 22(44), 23617-23626 (2012)
A Novel Synthesis of Rhodamine Derivatives.
Zhi-jian C and Xiao-jun P.
Liaoning Chemical Industry, 6 (2004)
Vanessa Jesus Ferreira et al.
Analytical methods : advancing methods and applications, 13(2), 267-273 (2020-12-29)
A method based on ultrasound-assisted emulsification liquid-liquid microextraction (USAEME) for cadmium determination by flame atomic absorption spectrometry (FAAS) was developed in this work. USAEME is based on the use of the mixture of 1,2-dichloroethane and trichloroethylene as an acceptor phase
Silyloxyamines as sources of silyl radicals: ESR spin-trapping, laser flash photolysis investigation, and photopolymerization ability.
Versace DL, et al.
Journal of Physical Organic Chemistry, 24(4), 342-350 (2011)
Xinyu Tian et al.
ChemPlusChem, 85(8), 1639-1645 (2020-08-05)
We report the synthesis, characterization, and photophysical and ion-binding properties of deep-red to near-infrared (NIR) fluorescent rhodamine derivatives, bearing two spirolactone rings and substitution of the oxygen atoms in the xanthene ring with sulfur atoms (1-S). The diastereoisomeric cis- and
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