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116068

Sigma-Aldrich

1-(2-Hydroxyethyl)piperidine

ReagentPlus®, 99%

Synonym(s):

1-Piperidineethanol, 2-Piperidinoethanol

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About This Item

Empirical Formula (Hill Notation):
C7H15NO
CAS Number:
3040-44-6
Molecular Weight:
129.20
Beilstein/REAXYS Number:
103390
EC Number:
221-244-6
MDL number:
MFCD00006512
UNSPSC Code:
12352100
PubChem Substance ID:
24847261
NACRES:
NA.22

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.)

SMILES string

OCCN1CCCCC1

InChI

1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2

InChI key

KZTWONRVIPPDKH-UHFFFAOYSA-N

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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

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

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

Certificates of Analysis (COA)

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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
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
A standard addition technique to quantify photoacid generation in chemically amplified photoresist.
Chemistry of Materials, 13(11), 4154-4162 (2001)
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