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Merck

34490

Sigma-Aldrich

Dibutylamine

puriss., ≥99.0% (GC)

Sinónimos:

N-Butyl-1-butanamine, n-Dibutylamine, Di-n-butylamine

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About This Item

Fórmula lineal:
(CH3CH2CH2CH2)2NH
Número de CAS:
Peso molecular:
129.24
Beilstein:
506001
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

densidad de vapor

4.46 (vs air)

Nivel de calidad

presión de vapor

1.9 mmHg ( 20 °C)

grado

puriss.

Ensayo

≥99.0% (GC)

temp. de autoignición

594 °F

lim. expl.

10 %

índice de refracción

n20/D 1.417 (lit.)
n20/D 1.417

bp

159 °C (lit.)

mp

−62 °C (lit.)

solubilidad

water: soluble 3.8 g/L at 20 °C

densidad

0.767 g/mL at 25 °C (lit.)

grupo funcional

amine

cadena SMILES

CCCCNCCCC

InChI

1S/C8H19N/c1-3-5-7-9-8-6-4-2/h9H,3-8H2,1-2H3

Clave InChI

JQVDAXLFBXTEQA-UHFFFAOYSA-N

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Aplicación

Dibutylamine was employed as organocatalyst during the synthesis of 2-amino-3-cyano-4H-chromen-4-ylphosphonates via Knoevenagel, Pinner and phospha-Michael reactions. Di-n-butylamine (Dibutylamine) may be used to investigate the performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter for airborne isocyanates. It was used in the preparation of 1M dibutylammonium phosphate buffer.

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

104.9 °F - closed cup

Punto de inflamabilidad (°C)

40.5 °C - closed cup

Equipo de protección personal

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


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Artículos

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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