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重要文件

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219703

Sigma-Aldrich

正己胺

99%

同義詞:

1-氨基己烷

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About This Item

線性公式:
CH3(CH2)5NH2
CAS號碼:
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

品質等級

200

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.)

官能基

amine

SMILES 字串

CCCCCCN

InChI

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

InChI 密鑰

BMVXCPBXGZKUPN-UHFFFAOYSA-N

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相關類別

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

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分析證明 (COA)

Lot/Batch Number
0000208723
0000188213
0000154051
0000139971
STBK4320

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存取文件庫

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
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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

Global Trade Item Number

庫存單位GTIN
219703-100ML4061837506796
219703-5ML4061838776075

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