72351
Benzyl nicotinate
≥98.0% (GC)
Synonym(s):
Nicotinic acid benzyl ester
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About This Item
Empirical Formula (Hill Notation):
C13H11NO2
CAS Number:
Molecular Weight:
213.23
Beilstein:
159169
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥98.0% (GC)
form
liquid
refractive index
n20/D 1.570
bp
177 °C/8 mmHg (lit.)
mp
24 °C (lit.)
functional group
ester
phenyl
SMILES string
O=C(OCc1ccccc1)c2cccnc2
InChI
1S/C13H11NO2/c15-13(12-7-4-8-14-9-12)16-10-11-5-2-1-3-6-11/h1-9H,10H2
InChI key
KVYGGMBOZFWZBQ-UHFFFAOYSA-N
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General description
Benzyl nicotinate is a benzyl ester. It is a vasodilator agent and is also generally used in cosmetics and drugs.
Application
Benzyl nicotinate can be used for the synthesis of benzylpalladium complexes to be used as catalysts for the substitution of olefins with benzylic groups.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
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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Blood flow enhancement in skin or oral mucosa after the topical application of liposome entrapped rubifacient as measured by EPR oximetry in vivo: the influence of size and liposome composition.
Marjeta Sentjurc
Cellular & molecular biology letters, 7(2), 256-258 (2002-07-05)
Milan Petelin et al.
International journal of pharmaceutics, 270(1-2), 83-91 (2004-01-17)
The aim of the present study was to determine the rate of transport and long-term effect of a drug applied to the oral mucosa in different ointments. Three ointments with bioadhesive properties: Orabase, Carbopol 935P, and polymethyl methacrylate (PMM) and
M A Kassem et al.
European journal of drug metabolism and pharmacokinetics, 5(1), 25-28 (1980-01-01)
The effect of benzyl nicotinate (15 mg) on the percutaneous absorption of dexamethasone 0,1 mg (62,5 uCi)/6 cm2, in an ethanol/octanol vehicle has been investigated in the rat. Both the urinary excretion and blood concentration data showed that benzyl nicotinate
Ute Jacobi et al.
Archives of dermatological research, 298(6), 291-300 (2006-09-13)
Cutaneous characteristics, e.g., thickness of the SC and density of follicles, affect the penetration of topically applied substances. In the present study, the penetration of benzyl nicotinate, causing a vasodilation, was studied on three anatomic sites (forearm, forehead and calf)
Francesca Palombo et al.
Journal of biomedical optics, 14(4), 044008-044008 (2009-09-04)
Diffusion of two model drugs-benzyl nicotinate and ibuprofen-and the plasma macromolecule albumin across atherosclerotic rabbit aorta was studied ex vivo by attenuated total reflection-Fourier transform infrared (ATR-FTIR) imaging. Solutions of these molecules were applied to the endothelial surface of histological
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