Skip to Content
Merck
All Photos(1)

Key Documents

122521

Sigma-Aldrich

3-Hydroxypyridine N-oxide

99%

Synonym(s):

3-Pyridinol N-oxide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H5NO2
CAS Number:
Molecular Weight:
111.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

190-192 °C (lit.)

SMILES string

Oc1ccc[n+]([O-])c1

InChI

1S/C5H5NO2/c7-5-2-1-3-6(8)4-5/h1-4,7H

InChI key

YMEZKRMAPQIBQH-UHFFFAOYSA-N

General description

3-Hydroxypyridine N-oxide exists in ethanol in the form of free base and in acid medium in the form of conjugate acid.

Application

3-Hydroxypyridine N-oxide was used to study the substrate specificity of dimethyl sulfoxide reductase, isolated from anaerobically grown Escherichia coli.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

J H Weiner et al.
Journal of bacteriology, 170(4), 1505-1510 (1988-04-01)
Dimethyl sulfoxide reductase, a terminal electron transfer enzyme, was purified from anaerobically grown Escherichia coli harboring a plasmid which codes for dimethyl sulfoxide reductase. The enzyme was purified to greater than 90% homogeneity from cell envelopes by a three-step purification
Structure and reactivity of 3-hydroxypyridine N-oxide.
Grachev VT, et al.
Chemistry of Heterocyclic Compounds, 10(1), 80-83 (1974)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service