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:
Molecular Weight:
165.23
Beilstein:
2717032
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥99%
form
solid
mp
54-58 °C (lit.)
SMILES string
CN(C)c1ccc(CCO)cc1
InChI
1S/C10H15NO/c1-11(2)10-5-3-9(4-6-10)7-8-12/h3-6,12H,7-8H2,1-2H3
InChI key
CDTPAAZQBPSVGS-UHFFFAOYSA-N
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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.
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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.
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