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Merck
CN

P66602

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:
586-98-1
Molecular Weight:
109.13
Beilstein:
107849
EC Number:
209-592-7
MDL number:
MFCD00006348
UNSPSC Code:
12352100
PubChem Substance ID:
24898786
NACRES:
NA.22

Key Documents

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Quality Level

200

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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General description

May darken in storage

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
STBD8554V
STBB4754V
STBB4754
S70237
S72237V

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Teruo Miyazaki et al.
Journal of clinical biochemistry and nutrition, 64(2), 112-123 (2019-04-03)
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
Masazumi Tamura et al.
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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