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E40609

Sigma-Aldrich

Ethyl nicotinate

99%

Sinonimo/i:

Nicotinic acid ethyl ester

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About This Item

Formula empirica (notazione di Hill):
C8H9NO2
Numero CAS:
614-18-6
Peso molecolare:
151.16
Beilstein:
122937
Numero CE:
210-370-7
Numero MDL:
MFCD00006389
Codice UNSPSC:
12352100
ID PubChem:
24894539
NACRES:
NA.22

Livello qualitativo

200

Saggio

99%

Stato

liquid

Indice di rifrazione

n20/D 1.504 (lit.)

P. ebollizione

223-224 °C (lit.)

Punto di fusione

8-10 °C (lit.)

Densità

1.107 g/mL at 25 °C (lit.)

Stringa SMILE

CCOC(=O)c1cccnc1

InChI

1S/C8H9NO2/c1-2-11-8(10)7-4-3-5-9-6-7/h3-6H,2H2,1H3
XBLVHTDFJBKJLG-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H314,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

199.4 °F - closed cup

Punto d’infiammabilità (°C)

93 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
STBK6970
STBK4130
STBJ6729
STBJ1994
STBH2344

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Kenji Sugibayashi et al.
Drug metabolism and pharmacokinetics, 19(5), 352-362 (2004-11-19)
The simultaneous diffusion and metabolism of ethyl nicotinate (EN) in a cultured human skin model, Living Skin Equivalent-high, was evaluated by the in vitro skin permeation and metabolism experiments, and esterase distribution was also determined. Theoretical calculations using Fick's 2nd
Tanasait Ngawhirunpat et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 58(3), 645-651 (2004-09-29)
The skin transport and metabolism characteristics of ethyl nicotinate (EN) in rabbit, rat, guinea-pig, pig, shed snake skin and human were compared. In vitro skin transport using excised skin and hydrolysis experiments using skin homogenate were carried out. Flux of
Tanasait Ngawhirunpat et al.
Biological & pharmaceutical bulletin, 26(9), 1311-1314 (2003-09-03)
The age and species dependent characteristics of cutaneous esterase activity were examined in cultured keratinocytes of neonatal and adult humans and of rats at the age of 1, 3, 10, and 50 d. The existence of esterases was characterized using
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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