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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

Quality Level

100

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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Related Categories

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

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
K. Tomizaki, et al.,
Chemistry Letters (Jpn), 37, 516-517 (2008)
T. Asakura, et al
J. Photopolym. Sci. Technol., 18, 407-414 (2005)
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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