219703
Hexylamine
99%
Synonym(s):
1-Aminohexane
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About This Item
Linear Formula:
CH3(CH2)5NH2
CAS Number:
Molecular Weight:
101.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-851-8
Beilstein/REAXYS Number:
1731298
MDL number:
Assay:
99%
Form:
liquid
Quality Level
assay
99%
form
liquid
expl. lim.
2.1-9.3 %
refractive index
n20/D 1.418 (lit.)
bp
131-132 °C (lit.)
mp
−23 °C (lit.)
density
0.766 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCCCCCN
InChI
1S/C6H15N/c1-2-3-4-5-6-7/h2-7H2,1H3
InChI key
BMVXCPBXGZKUPN-UHFFFAOYSA-N
Application
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.
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wgk
WGK 1
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
Storage Class
3 - Flammable liquids
flash_point_f
80.6 °F - closed cup
flash_point_c
27 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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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)
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 219703-100ML | 04061837506796 |
| 219703-5ML | 04061838776075 |