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Merck
CN

471232

二丁胺

≥99.5%

别名:

N,N-二-n-丁胺

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关于此项目

线性分子式:
(CH3CH2CH2CH2)2NH
化学文摘社编号:
分子量:
129.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-921-8
Beilstein/REAXYS Number:
506001
MDL number:
Assay:
≥99.5%
Bp:
159 °C (lit.)
Vapor pressure:
1.9 mmHg ( 20 °C)
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vapor density

4.46 (vs air)

Quality Level

vapor pressure

1.9 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

594 °F

expl. lim.

10 %

refractive index

n20/D 1.417 (lit.)

pH

11.1 (20 °C, 1 g/L)

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

SMILES string

CCCCNCCCC

InChI

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

InChI key

JQVDAXLFBXTEQA-UHFFFAOYSA-N

General description

二丁胺是一种高活性的催化剂,通常用作异氰酸酯衍生化反应中的试剂。

Application

二丁胺可用作反应物以合成:通过与芳基氯化物和溴化物的 Pd 催化 Buchwald-Hartwig 胺化反应合成
  • N, N




  • -二丁基-4-甲基苯胺。     
  • 通过与乙酸异丙烯酯的乙酰化反应合成 N,N-二丁基二乙酰胺。

也可用作:      
  • 不同消除反应中的强阻碍碱。
  • 有机催化剂,通过芳香族醛、丙二腈和巴比妥酸的多组分缩合反应合成环状吡喃 [2,3-d] 嘧啶衍生物。



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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

危险化学品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Determination of complex mixtures of airborne isocyanates and amines. Part 1. Liquid chromatography with ultraviolet detection of monomeric and polymeric isocyanates as their dibutylamine derivatives.
Spanne M, et al.
Analyst, 121(8), 1095-1099 (1996)
Chemistry of blocked isocyanates. II. Kinetics and mechanism of the reaction of dibutylamine with phenyl and 2-methylphenyl oxime carbamates.
Levine AW and Fech Jr J.
The Journal of Organic Chemistry, 37(15), 2455-2460 (1972)
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



全球贸易项目编号

货号GTIN
471232-500ML04061832359663
471232-100ML04061832359649
471232-18L04061836827021
471232-1L04061832359656