E40609
Ethyl nicotinate
99%
Synonym(s):
Nicotinic acid ethyl ester
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All Photos(3)
About This Item
Empirical Formula (Hill Notation):
C8H9NO2
CAS Number:
Molecular Weight:
151.16
Beilstein:
122937
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
refractive index
n20/D 1.504 (lit.)
bp
223-224 °C (lit.)
mp
8-10 °C (lit.)
density
1.107 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)c1cccnc1
InChI
1S/C8H9NO2/c1-2-11-8(10)7-4-3-5-9-6-7/h3-6H,2H2,1H3
InChI key
XBLVHTDFJBKJLG-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
199.4 °F - closed cup
Flash Point(C)
93 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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K Sugibayashi et al.
Journal of controlled release : official journal of the Controlled Release Society, 62(1-2), 201-208 (1999-10-16)
An in vitro permeation study of ethyl nicotinate (EN) was carried out using excised hairless rat skin, and simultaneous skin transport and metabolism of the drug were kinetically followed. Fairly good steady-state fluxes of EN and its metabolite nicotinic acid
Ibrahim Uçar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(1), 11-16 (2008-11-18)
Mononuclear copper(II) saccharinate (sac) complex containing ethylnicotinate (enc), [Cu(enc)(2)(sac)(2)(H(2)O)].1.4H(2)O has been synthesized and characterized by spectroscopic (IR, UV-vis, EPR), X-ray diffraction technique and electrochemical methods. It crystallizes in the tetragonal crystal systems with space group I4(1)cd and Z=8. The copper(II)
S Y Chan et al.
Skin pharmacology : the official journal of the Skin Pharmacology Society, 6(4), 298-312 (1993-01-01)
Pulsed-light reflectance using the Minolta Chroma Meter CR-200 was evaluated as a quantitative method for the noninvasive assessment of drug-induced erythema on the flexor surface of the forearm. Nicotinate esters were used as model vasodilators. Several parameters derived from the
Tetsuya Hasegawa et al.
Biological & pharmaceutical bulletin, 31(1), 85-89 (2008-01-08)
The skin disposition and metabolism of topically applied ethyl nicotinate (EN) were evaluated in dual agar gel disc-inserted hairless rats, which have two agar gel discs subcutaneously inserted into the abdominal region as drug receptors, and a topical formulation containing
K Sugibayashi et al.
Pharmaceutical research, 13(6), 855-860 (1996-06-01)
Simultaneous skin transport and metabolism of ethyl nicotinate (EN), a model drug, were measured and theoretically analyzed. Several permeation studies of EN or its metabolite nicotinic acid (NA) were done on full-thickness skin or stripped skin with and without an
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