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E40609

Sigma-Aldrich

Ethyl nicotinate

99%

Synonym(s):

Nicotinic acid ethyl ester

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About This Item

Empirical Formula (Hill Notation):
C8H9NO2
CAS Number:
614-18-6
Molecular Weight:
151.16
Beilstein/REAXYS Number:
122937
EC Number:
210-370-7
MDL number:
MFCD00006389
UNSPSC Code:
12352100
PubChem Substance ID:
24894539
NACRES:
NA.22

Quality Level

200

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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Related Categories

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB1960
STBK6970
STBK4130
STBJ6729
STBJ1994

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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)
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
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
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
Adel S Girgis et al.
European journal of medicinal chemistry, 43(9), 1818-1827 (2008-02-05)
2-(alicyclic-amino)-4,6-diaryl-3-pyridinecarboxylates 5a-d were prepared via aromatic nucleophilic substitution reaction of secondary amines (piperidine or morpholine) with 2-bromo-3-pyridinecarboxylate derivatives 3a,b. The latters were obtained through bromination of 3-aryl-4-benzoyl-2-cyanobutyrates 2a and 2b, which were obtained from the base promoted addition of ethyl
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