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Merck
CN

34490

二丁胺

puriss., ≥99.0% (GC)

别名:

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

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关于此项目

线性分子式:
(CH3CH2CH2CH2)2NH
化学文摘社编号:
111-92-2
分子量:
129.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329754984
EC Number:
203-921-8
Beilstein/REAXYS Number:
506001
MDL number:
MFCD00009429
Assay:
≥99.0% (GC)

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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 %

Quality Level

200

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

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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

存储类别

3 - Flammable liquids

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

Hazard Classifications

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN2998
BCCH3503
BCCG6831
BCCF5564
BCCD8695

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Daniel Gylestam et al.
The Annals of occupational hygiene, 58(1), 28-49 (2013-08-21)
The performance of a dry sampler, with an impregnated denuder in series with a glass fibre filter, using di-n-butylamine (DBA) for airborne isocyanates (200ml min(-1)) is investigated and compared with an impinger flask with a glass fibre filter in series
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
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
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
Asa Marand et al.
Journal of environmental monitoring : JEM, 7(4), 335-343 (2005-03-31)
The solvent-free sampler for airborne isocyanates consisted of a polypropylene tube with an inner wall coated with a glass fibre filter, coupled in series with a 13 mm glass fibre filter. The filters were impregnated with reagent solution containing equimolar
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Knoevenagel Condensation Reaction

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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