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Merck

E40609

Sigma-Aldrich

Ethylnikotinat

99%

Synonym(e):

Ethyl-nicotinat

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About This Item

Empirische Formel (Hill-System):
C8H9NO2
CAS-Nummer:
Molekulargewicht:
151.16
Beilstein:
122937
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.504 (lit.)

bp

223-224 °C (lit.)

mp (Schmelzpunkt)

8-10 °C (lit.)

Dichte

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

InChIKey

XBLVHTDFJBKJLG-UHFFFAOYSA-N

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Piktogramme

CorrosionExclamation mark

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

199.4 °F - closed cup

Flammpunkt (°C)

93 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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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
R Fleming et al.
Journal of pharmaceutical sciences, 72(2), 142-145 (1983-02-01)
The kinetic barrier against the transport of methyl and ethyl nicotinates across the water-isopropyl myristate interface has been studied as a function of temperature using a rotating diffusion cell. The temperature dependence of the interfacial transfer kinetics has enabled calculation
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)
Zuleikha A M Nworgu et al.
Acta poloniae pharmaceutica, 64(2), 179-182 (2007-08-02)
3-Carbomethoxypyridine (CMP) was isolated and characterized from the leaves of Pyrenacantha staudtii Hutch and Dalz, family Icacinaceae, in our earlier study and was found to possess an inhibitory activity on the isolated rat uterus. In order to study the structure
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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