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Merck
CN

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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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%
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产品名称

N-羟乙基哌啶, ReagentPlus®, 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

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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

pictograms

Exclamation mark

signalword

Warning

hcodes

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

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分析证书(COA)

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T. Asakura, et al
J. Photopolym. Sci. Technol., 18, 407-414 (2005)
K. Tomizaki, et al.,
Chemistry Letters (Jpn), 37, 516-517 (2008)
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
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
Hongxia Cui et al.
Journal of pharmaceutical sciences, 104(10), 3395-3403 (2015-09-10)
The study was carried out to investigate the mechanism of the ion-pair strategy in modulating zaltoprofen (ZAL) skin permeability. Seven organic amines were chosen as counter ions and the formation of ion pairs was confirmed by Fourier transform infrared and

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