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Key Documents

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:
Molecular Weight:
129.20
Beilstein:
103390
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

156.2 °F - closed cup

Flash Point(C)

69 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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