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H56800

2-Hydroxypyridine

Name: 2-Hydroxypyridine
Brand: ALDRICH

97%

Synonym(s):

2(1H)-Pyridone, 2-Pyridinol

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About This Item

Empirical Formula (Hill Notation):

C₅H₅NO

CAS Number:

142-08-5

Molecular Weight:

95.10

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895704

EC Number:

205-520-3

Beilstein/REAXYS Number:

105757

MDL number:

MFCD00006268

Assay:

97%

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Properties

Quality Level

200

assay

97%

bp

280-281 °C (lit.)

mp

105-107 °C (lit.)

SMILES string

Oc1ccccn1

InChI

1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)

InChI key

UBQKCCHYAOITMY-UHFFFAOYSA-N

Description

Application

Catalyst for generating β-oxopropyl carbonates from cyclic carbonates and alcohols and in the aminolysis of a polyglutamate.

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pictograms

GHS06

signalword

Danger

hcodes

H301

pcodes

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Polymer, 35, 2443-2443 (1994)

Journal of the Chemical Society. Perkin Transactions 1, 1749-1749 (1993)

Different STAT Transcription Complexes Drive Early and Delayed Responses to Type I IFNs.

Ali A Abdul-Sater et al.

Journal of immunology (Baltimore, Md. : 1950), 195(1), 210-216 (2015-05-29)

IFNs, which transduce pivotal signals through Stat1 and Stat2, effectively suppress the replication of Legionella pneumophila in primary murine macrophages. Although the ability of IFN-γ to impede L. pneumophila growth is fully dependent on Stat1, IFN-αβ unexpectedly suppresses L. pneumophila

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Global Trade Item Number

SKU	GTIN
H56800-100G	04061838354723
H56800-25G	04061833076453