Skip to Content
MilliporeSigma
All Photos(4)

Key Documents

M59203

Sigma-Aldrich

Methyl nicotinate

99%

Synonym(s):

Nicotinic acid methyl ester

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C7H7NO2
CAS Number:
Molecular Weight:
137.14
Beilstein/REAXYS Number:
113951
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

biological source

synthetic

Quality Level

assay

99%

form

powder or crystals (possibly with chunks)

color

white to faint yellow

bp

204 °C (lit.)

mp

42-44 °C (lit.)

SMILES string

COC(=O)c1cccnc1

InChI

1S/C7H7NO2/c1-10-7(9)6-3-2-4-8-5-6/h2-5H,1H3

InChI key

YNBADRVTZLEFNH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Methyl nicotinate (or nicotinic acid methyl ester) is used as a rubefacient for the relief of pains in muscles, tendons, and joints. It is also used in food as a flavoring agent.

Application

Methyl nicotinate can be employed as a precursor in the synthesis:
  • Di-3-pyridyl ketone ligand, which is used in the preparation of silver(I) complexes for the derivation of coordination polymeric chains.
  • 5-arylnicotinates , ±-sesbanine , and 1,4-dihydropyridine derivatives.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

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

Synthesis of 3, 5-diacyl-4-phenyl-1, 4-dihydropyridines
Bennasar M-L, et al.
Tetrahedron Letters, 39(50), 9275-9278 (1998)
Helical and zigzag coordination polymeric chains derived from di-3-pyridyl ketone and silver (I) salts
Chen X-D and Mak Thomas CW
Journal of Molecular Structure, 743(1-3), 1-6 (2005)
Topical antirheumatic agents as hydroxyl radical scavengers
Billany MR, et al.
International Journal of Pharmaceutics, 124(2), 279-283 (1995)
A facile synthesis of ? -sesbanine via γ-addition of ketene silyl acetal with quaternized methyl nicotinate
Wada M, et al.
Tetrahedron Letters, 26(27), 3267-3270 (1985)
A general synthesis of 5-arylnicotinates
Thompson WJ and Gaudino J
The Journal of Organic Chemistry, 49(26), 5237-5243 (1984)

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