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
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.[3]
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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M Krzic et al.
Journal of controlled release : official journal of the Controlled Release Society, 70(1-2), 203-211 (2001-02-13)
The development of formulations, which increase skin oxygenation and of methods for measuring oxygen levels in skin are important for dealing with processes affected by the level of oxygen, e.g., rate of healing and efficiency of radiation oncology. In this
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
K Wirén et al.
The British journal of dermatology, 160(3), 552-556 (2009-01-06)
The cosmetic properties of topical formulations are important parameters for the adherence to treatment, where modern oil-in-water emulsions are considered more acceptable compared with ointments. After application of an emulsion to the skin, the concentration of active ingredients in the
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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