72420
Methyl nicotinate
puriss., ≥99.0% (GC)
Synonym(s):
Nicotinic acid methyl ester
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About This Item
Empirical Formula (Hill Notation):
C7H7NO2
CAS Number:
Molecular Weight:
137.14
Beilstein:
113951
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
biological source
synthetic
Quality Level
grade
puriss.
Assay
≥99.0% (GC)
form
powder or crystals (possibly with chunks)
color
white to faint yellow
bp
204 °C (lit.)
mp
39-42 °C
42-44 °C (lit.)
solubility
H2O: 0.1 g/mL, clear
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
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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 used as a precursor:
- In the asymmetric synthesis of 1-azasugars (glycosidase inhibitors) for biomedical applications.
- In the total synthesis of ±-sesbanine.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
Topical antirheumatic agents as hydroxyl radical scavengers
Billany MR, et al.
International Journal of Pharmaceutics, 124(2), 279-283 (1995)
Selective fowler reductions: asymmetric total syntheses of isofagomine and other 1-azasugars from methyl nicotinate
Zhao G, et al.
Organic Letters, 3(2), 201-203 (2001)
Paola Ziosi et al.
Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI), 12(4), 303-308 (2006-10-10)
Skin antioxidant network protects cells against oxidative injury and prevents the production of oxidation products. When oxidative stress overwhelms the skin antioxidant capacity, the subsequent modification of the cellular redox apparatus leads to an alteration of cell homeostasis leading to
Melissa Kerr et al.
Prostaglandins, leukotrienes, and essential fatty acids, 79(1-2), 15-19 (2008-07-29)
Topical application of nicotinic acid results in erythema, and in some cases oedema of the skin, supporting a strong relationship between niacin sensitivity and prostaglandin D2. The aim of this study was to examine the inter-rater and intra-rater reliability of
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