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Merck

34490

Dibutylamine

puriss., ≥99.0% (GC)

Sinónimos:

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

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Fórmula lineal:
(CH3CH2CH2CH2)2NH
Número CAS:
111-92-2
Peso molecular:
129.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329754984
EC Number:
203-921-8
Beilstein/REAXYS Number:
506001
MDL number:
MFCD00009429

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Nombre del producto

Dibutylamine, puriss., ≥99.0% (GC)

InChI key

JQVDAXLFBXTEQA-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCNCCCC

vapor density

4.46 (vs air)

vapor pressure

1.9 mmHg ( 20 °C)

grade

puriss.

assay

≥99.0% (GC)

autoignition temp.

594 °F

expl. lim.

10 %

refractive index

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

bp

159 °C (lit.)

mp

−62 °C (lit.)

solubility

water: soluble 3.8 g/L at 20 °C

density

0.767 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

200

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Application

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.

signalword

Danger

Hazard Classifications

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

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 1

flash_point_f

104.9 °F - closed cup

flash_point_c

40.5 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCN2998
BCCH3503
BCCG6831
BCCF5564
BCCD8695

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Reddi Mohan Naidu Kalla et al.
European journal of medicinal chemistry, 76, 61-66 (2014-02-27)
A series of 2-amino-3-cyano-4H-chromen-4-ylphosphonates have been synthesized by reacting substituted salicylaldehydes, malononitrile, and dialkylphosphites using a catalytic amount of dibutylamine as an organocatalyst employing Knoevenagel, Pinner, and phospha-Michael reactions simultaneously in ethanol. This protocol is an environmentally friendly procedure and
C M Stobba-Wiley et al.
Journal of AOAC International, 83(4), 837-846 (2000-09-20)
A method was developed and validated for determination and quantitation of tilmicosin residues in swine, cattle, and sheep edible tissues, as well as chicken fat, skin, and muscle over a concentration range of 0.025 microg/g-20 microg/g. For chicken kidney and
Baiyi Xue et al.
Journal of mass spectrometry : JMS, 46(7), 689-695 (2011-07-12)
Characterization of glycosaminoglycans poses a challenge for current analytical techniques, as they are highly acidic, polydisperse and heterogeneous compounds. The purpose of this study is the separation and analysis of a partially depolymerized heparin-like glycosaminoglycan by on-line ion-pairing reversed-phase high-performance
J T Fitzsimons et al.
Comparative biochemistry and physiology. A, Comparative physiology, 93(1), 285-290 (1989-01-01)
1. Ultrastructural changes in liver tissue of mice fed nitrosamine precursors, dibutylamine and nitrite, were observed. 2. The protective effect of soyabean in a diet containing nitrosamine precursors was demonstrated. 3. Liver tissue was examined to investigate the anticarcinogenicity of
Er Bei et al.
Water research, 183, 116055-116055 (2020-07-06)
N-nitrosodimethylamine (NDMA) as one emerging disinfection by-product has been investigated globally since 1990s. However, its main precursors are still unclear. We found that NDMA formation potential (NDMAFP) of various water samples increased firstly and then decreased gradually during incubation with
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