跳转至内容
Merck
所有图片(2)

Key Documents

更多文件

219703

Sigma-Aldrich

正己胺

99%

别名:

1-氨基己烷

登录查看公司和协议定价
所有图片(2)

About This Item

线性分子式:
CH3(CH2)5NH2
CAS号:
111-26-2
分子量:
101.19
Beilstein:
1731298
EC號碼:
203-851-8
MDL號碼:
MFCD00008240
分類程式碼代碼:
12352100
PubChem物質ID:
24853140
NACRES:
NA.22

化驗

99%

形狀

liquid

expl. lim.

2.1-9.3 %

折射率

n20/D 1.418 (lit.)

bp

131-132 °C (lit.)

mp

−23 °C (lit.)

密度

0.766 g/mL at 25 °C (lit.)

SMILES 字串

CCCCCCN

InChI

1S/C6H15N/c1-2-3-4-5-6-7/h2-7H2,1H3

InChI 密鑰

BMVXCPBXGZKUPN-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

相关类别

應用

己胺可用于：
  • 作为引发剂，通过伯胺引发的N-羧基酸酐开环聚合反应合成精确(defined)聚肽。
  • 作为反应剂，通过酰胺键形成反应对多晶金表面的烷基硫醇单层进行改性。
  • 官能化MWCNT、氧化石墨烯和聚氨酯表面。这些官能化复合材料可用于吸附、CO2捕集，以及作为阻隔材料。

訊號詞

Danger

危險分類

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

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 1

閃點（°F）

80.6 °F - closed cup

閃點（°C）

27 °C - closed cup

個人防護裝備

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

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Adsorption behaviour of n-hexylamine at the Hg/water interphase and its comparison with a molecular model accounting for local order.
Carla M, et al.
J. Electroanal. Chem. Interfac. Electrochem., 197(1), 123-141 (1986)
Jiong Zou et al.
Macromolecules, 46(10), 4223-4226 (2013-06-25)
A facile N
Julien Roeser et al.
Rapid communications in mass spectrometry : RCM, 27(4), 546-552 (2013-01-17)
Cleavage of peptide bonds C-terminal to tyrosine and tryptophan after electrochemical oxidation may become a complementary approach to chemical and enzymatic cleavage. A chemical labeling approach specifically targeting reactive cleavage products is presented here and constitutes a promising first step
Leon Coulier et al.
Analytical chemistry, 78(18), 6573-6582 (2006-09-15)
We have developed an analytical method, consisting of ion-pair liquid chromatography coupled to electrospray ionization mass spectrometry (IP-LC-ESI-MS), for the simultaneous quantitative analysis of several key classes of polar metabolites, like nucleotides, coenzyme A esters, sugar nucleotides, and sugar bisphosphates.
J P Wolfe et al.
The Journal of organic chemistry, 65(4), 1144-1157 (2000-05-18)
Mixtures of Pd(2)(dba)(3) or Pd(OAc)(2) and BINAP catalyze the cross-coupling of amines with a variety of aryl bromides. Primary amines are arylated in high yield, and certain classes of secondary amines are also effectively transformed. The process tolerates the presence
查看所有相关文献

实验方案

Catalytic Amide Bond Formation Protocol

Information on the Amide bond and the Catalytic Amide Bond Formation Protocol. Amidation of amines and alcohols. The amide bond, an important linkage in organic chemistry, is a key functional group in peptides, polymers, and many natural products and pharmaceuticals.

GC Analysis of Primary Amines on Carbowax® Amine

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门