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Key Documents

P66602

Sigma-Aldrich

2-Pyridinemethanol

98%

Synonym(s):

ω-Hydroxy-2-picoline, 2-(Hydroxymethyl)pyridine, 2-Pyridyl carbinol

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About This Item

Empirical Formula (Hill Notation):
C6H7NO
CAS Number:
Molecular Weight:
109.13
Beilstein:
107849
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.543 (lit.)

bp

112-113 °C/16 mmHg (lit.)

density

1.131 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

OCc1ccccn1

InChI

1S/C6H7NO/c8-5-6-3-1-2-4-7-6/h1-4,8H,5H2

InChI key

SHNUBALDGXWUJI-UHFFFAOYSA-N

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Physical properties

May darken in storage

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Teruo Miyazaki et al.
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Nuclear receptor farnesoid X receptor activation inhibits fatty acid synthesis through the liver X receptor-α-sterol regulatory element binding protein-1c pathway universally in animals, but also has human-specific crosstalk with the peroxisome proliferator-activated receptor-α. The effects of farnesoid X receptor-ligands on
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Nature communications, 6, 8580-8580 (2015-10-06)
Multidentate materials formed by simply mixing heterogeneous and homogeneous components are promising for construction of versatile active sites on the surface of heterogeneous compounds, however, to the best of our knowledge, there are no reports on such materials. Self-assembly of

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