추천 제품
Quality Level
분석
99%
형태
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.)
작용기
amine
SMILES string
CCCCCCN
InChI
1S/C6H15N/c1-2-3-4-5-6-7/h2-7H2,1H3
InChI key
BMVXCPBXGZKUPN-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
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.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
80.6 °F - closed cup
Flash Point (°C)
27 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
Adsorption behaviour of n-hexylamine at the Hg/water interphase and its comparison with a molecular model accounting for local order.
J. Electroanal. Chem. Interfac. Electrochem., 197(1), 123-141 (1986)
Macromolecules, 46(10), 4223-4226 (2013-06-25)
A facile N
Transformer oil based multi-walled carbon nanotube-hexylamine coolant with optimized electrical, thermal and rheological enhancements
Royal Society of Chemistry Advances, 5(130), 107222-107236 (2015)
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(5-6), 326-334 (2011-01-22)
A liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for determination of the new anticancer agent picropodophyllin (AXL1717) and its isomer podophyllotoxin levels in human serum has been developed. Monitoring of hexylamine adducts rather than proton adducts was used to optimize sensitivity.
The Journal of organic chemistry, 67(23), 8151-8156 (2002-11-09)
Several functional groups were introduced on the upper rim of (lower rim free) homooxacalix[3]arene for the first time. The swinging nitrohomooxacalix[3]arene host 1 was fixed in the cone conformation by complexation with n-hexylamine.
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