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B25606

Sigma-Aldrich

N-Benzylmethylamine

97%

Sinônimo(s):

N-Methylbenzylamine

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About This Item

Fórmula linear:
C6H5CH2NHCH3
Número CAS:
103-67-3
Peso molecular:
121.18
Beilstein:
606221
Número CE:
203-133-4
Número MDL:
MFCD00008289
Código UNSPSC:
12352100
ID de substância PubChem:
24891660
NACRES:
NA.22

Ensaio

97%

forma

liquid

índice de refração

n20/D 1.522 (lit.)

pb

184-189 °C (lit.)

densidade

0.939 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CNCc1ccccc1

InChI

1S/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H3

chave InChI

RIWRFSMVIUAEBX-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Health hazardCorrosion
GHS08,GHS05

Palavra indicadora

Danger

Frases de perigo

H314,H317,H334

Classificações de perigo

Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

167.0 °F - closed cup

Ponto de fulgor (°C)

75 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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F Karoum
British journal of pharmacology, 90(2), 335-345 (1987-02-01)
In an effort to explore the contribution of the metabolites of pargyline towards the in vivo inhibition of monoamine oxidase (MAO), the effects of pargyline and its major metabolites on the production and metabolism of a number of biogenic amines
T Tahira et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(6), 511-516 (1988-06-01)
Thioproline, which is readily nitrosated to form nitrosothioproline, is expected to act as a nitrite scavenger. The effect of thioproline as an inhibitor of the carcinogenesis induced by N-nitroso-N-benzylmethylamine precursors was examined. Two groups of male F-344 rats were given
C C Hsia et al.
Proceedings of the National Academy of Sciences of the United States of America, 78(3), 1878-1881 (1981-03-01)
Previous studies in Linxian, an area of China with a high incidence of esophageal carcinoma, showed that fungal infections are common in the esophageal epithelium of patients with either premalignant changes or early esophageal carcinoma. Fungi of the genus Candida
R Siegler et al.
Journal of pharmaceutical and biomedical analysis, 7(1), 45-55 (1989-01-01)
DTAF has been used successfully to prepare fluorescent labelled reagents for fluorescence polarization immunoassays. Its applicability as a derivation reagent for direct fluorescence analysis of primary and secondary amines was evaluated. DTAF was shown to have spectral properties that closely
H Weber et al.
Journal of chromatography, 307(1), 145-153 (1984-04-13)
The separation of racemic benoxaprofen into the two benoxaprofen enantiomers by preparative high-performance liquid chromatography and the application of the activated enantiomers as derivatization reagents for the simultaneous stereoselective determination of chiral amines in biological material is described. Activated (+)-
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