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Merck

219703

Sigma-Aldrich

Hexylamin

99%

Synonym(e):

1-Amino-hexan

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About This Item

Lineare Formel:
CH3(CH2)5NH2
CAS-Nummer:
Molekulargewicht:
101.19
Beilstein:
1731298
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

99%

Form

liquid

Expl.-Gr.

2.1-9.3 %

Brechungsindex

n20/D 1.418 (lit.)

bp

131-132 °C (lit.)

mp (Schmelzpunkt)

−23 °C (lit.)

Dichte

0.766 g/mL at 25 °C (lit.)

SMILES String

CCCCCCN

InChI

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

InChIKey

BMVXCPBXGZKUPN-UHFFFAOYSA-N

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Anwendung

Hexylamine can be used:
  • As an initiator to synthesize defined polypeptides by primary amine-initiated N-carboxyanhydride ring opening polymerization reaction.
  • As a reactant to modify alkanethiol monolayers at polycrystalline gold surfaces via amide bond formation reaction.
  • To functionalize the surface of MWCNT, graphene oxide, and polyurethanes. These functionalized composites materials find applications in absorption, CO2 capture, and as barrier materials.

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

80.6 °F - closed cup

Flammpunkt (°C)

27 °C - closed cup

Persönliche Schutzausrüstung

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


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Kunden haben sich ebenfalls angesehen

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

Protokolle

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.

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

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