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Merck
CN

347590

2-[4-(Dimethylamino)phenyl]ethanol

≥99%

Synonym(s):

4-(Dimethylamino)phenethyl alcohol

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About This Item

Linear Formula:
(CH3)2NC6H4CH2CH2OH
CAS Number:
50438-75-0
Molecular Weight:
165.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24861514
MDL number:
MFCD00009711
Beilstein/REAXYS Number:
2717032

Key Documents

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Product Name

2-[4-(Dimethylamino)phenyl]ethanol, ≥99%

InChI

1S/C10H15NO/c1-11(2)10-5-3-9(4-6-10)7-8-12/h3-6,12H,7-8H2,1-2H3

SMILES string

CN(C)c1ccc(CCO)cc1

InChI key

CDTPAAZQBPSVGS-UHFFFAOYSA-N

assay

≥99%

form

solid

mp

54-58 °C (lit.)

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Application

2-[4-(Dimethylamino)phenyl]ethanol (4-(Dimethylamino)phenethyl alcohol) may be used as accelerator to investigate the the curing of bone cement at molecular level by electron spin resonance (ESR) spectroscopy. 2-[4-(Dimethylamino)phenyl]ethanol (4-(N,N-dimethylamino)phenethyl alcohol) may be used to compare the efficiency of different camphorquinone (CQ)/amine photo-initiating systems for the photopolymerization of a model dental resin.

General description

2-[4-(Dimethylamino)phenyl]ethanol (4-(Dimethylamino)phenethyl alcohol) is a more effective accelerator than N,N-dimethyl-p-toluidine (TD) for bone cement curing.

signalword

Warning

pictograms

Exclamation mark
GHS07

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5691
S79984V
MKBK5411V
STBB4355V
S80607V

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F F Oldfield et al.
Journal of biomedical materials research, 44(4), 436-445 (1999-07-09)
Electron spin resonance (ESR) spectroscopy was used to gain insight at the molecular level into the curing of bone cement. Methyl methacrylate was polymerized using a N,N-dimethyl-p-toluidine (TD)/benzoyl peroxide (BPO) redox system in the presence of polymethyl methacrylate (PMMA) powder.
Walter F Schroeder et al.
Dental materials : official publication of the Academy of Dental Materials, 23(10), 1313-1321 (2006-12-19)
The aim of this study was to compare the efficiency of different camphorquinone (CQ)/amine photo-initiating systems for the photopolymerization of a model dental resin based in Bis-GMA/TEGDMA. The monomer conversion versus exposure time was measured in resins containing different types

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