Pular para o conteúdo
Merck
Todas as fotos(3)

Documentos Principais

Visualizar Toda a Documentação

E40609

Sigma-Aldrich

Ethyl nicotinate

99%

Sinônimo(s):

Nicotinic acid ethyl ester

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(3)

About This Item

Fórmula empírica (Notação de Hill):
C8H9NO2
Número CAS:
614-18-6
Peso molecular:
151.16
Beilstein:
122937
Número CE:
210-370-7
Número MDL:
MFCD00006389
Código UNSPSC:
12352100
ID de substância PubChem:
24894539
NACRES:
NA.22

Nível de qualidade

200

Ensaio

99%

Formulário

liquid

índice de refração

n20/D 1.504 (lit.)

p.e.

223-224 °C (lit.)

pf

8-10 °C (lit.)

densidade

1.107 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCOC(=O)c1cccnc1

InChI

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

chave InChI

XBLVHTDFJBKJLG-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Categorias relacionadas

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Frases de perigo

H314,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

199.4 °F - closed cup

Ponto de fulgor (°C)

93 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
STBK6970
STBK4130
STBJ6729
STBJ1994
STBH2344

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 6

1 of 6

Ethyl isonipecotate 98%

Sigma-Aldrich

E33505

Ethyl isonipecotate

(−)-Nicotine solution 1.0 mg/mL, analytical standard, for drug analysis

Supelco

N5511

(−)-Nicotine solution

Eugenol ≥98%, FCC, FG

Sigma-Aldrich

W246700

Eugenol

1-Iodobutane 99%, contains copper as stabilizer

Sigma-Aldrich

167304

1-Iodobutane

Isonicotinic acid 99%

Sigma-Aldrich

I17508

Isonicotinic acid

1-Vinil-2-pirrolidinona contains sodium hydroxide as inhibitor, ≥99%

Sigma-Aldrich

V3409

1-Vinil-2-pirrolidinona

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
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica