116068
N-羟乙基哌啶
ReagentPlus®, 99%
别名:
1-哌啶乙醇, N-哌啶乙醇
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关于此项目
经验公式（希尔记法）:
C7H15NO
化学文摘社编号:
分子量:
129.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-244-6
Beilstein/REAXYS Number:
103390
MDL number:
Assay:
99%
InChI key
KZTWONRVIPPDKH-UHFFFAOYSA-N
InChI
1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2
SMILES string
OCCN1CCCCC1
product line
ReagentPlus®
assay
99%
refractive index
n20/D 1.4804 (lit.)
bp
199-202 °C (lit.)
density
0.973 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
Application
1-(2-Hydroxyethyl)piperidine (1-Piperidineethanol) has been used as the base quencher to determine the efficiency of the decomposition of photoacid generators.
Counter-ion used for investigations of skin permeation of flurbiprofen
Catalyst used for enantioselective synthesis
Amine quencher used during synthesis of photoacid generators for ArF lithography
Adsorbent for capture and release of pressurized carbon dioxide for greenhouse gas control
Catalyst used for enantioselective synthesis
Amine quencher used during synthesis of photoacid generators for ArF lithography
Adsorbent for capture and release of pressurized carbon dioxide for greenhouse gas control
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Xu Ma et al.
Journal of pharmaceutical sciences, 99(4), 1826-1837 (2009-11-07)
The aim of this work was to investigate the percutaneous absorption of flurbiprofen (FP) using counter-ions as enhancers as well as to compare their enhancing activity with penetration enhancers in vitro. The in vitro permeation studies of FP were performed
A standard addition technique to quantify photoacid generation in chemically amplified photoresist.
Chemistry of Materials, 13(11), 4154-4162 (2001)
François Lutz et al.
Journal of the American Chemical Society, 127(35), 12206-12207 (2005-09-01)
An asymmetric autocatalytic reaction has been catalyzed by a mixture of chiral and achiral beta-amino alcohols. The absolute configuration of the highly enantioenriched obtained product (>98% ee) was shown to depend not only on the absolute configuration of the chiral
T. Asakura, et al
J. Photopolym. Sci. Technol., 18, 407-414 (2005)
K. Tomizaki, et al.,
Chemistry Letters (Jpn), 37, 516-517 (2008)
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