52270
1-十六烷硫醇
≥95.0% (GC)
别名:
十六烷基硫醇, 十六硫醇, 正十六硫醇
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关于此项目
线性分子式:
CH3(CH2)15SH
化学文摘社编号:
分子量:
258.51
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-846-6
Beilstein/REAXYS Number:
1748495
MDL number:
Assay:
≥95.0% (GC)
InChI key
ORTRWBYBJVGVQC-UHFFFAOYSA-N
InChI
1S/C16H34S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3
SMILES string
CCCCCCCCCCCCCCCCS
assay
≥95.0% (GC)
refractive index
n20/D 1.462 (lit.), n20/D 1.464
bp
184-191 °C/7 mmHg (lit.)
mp
18-20 °C (lit.)
transition temp
solidification point 15-18 °C(lit.)
density
0.84 g/mL at 25 °C (lit.)
functional group
thiol
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Application
1-十六硫醇已用于制备胆固醇-PIE12-三聚体和烷基-PIE12-三聚体（PIE12-三聚体 = 蛋白酶抗性三聚体 D 肽抑制剂）。它可用于银纳米线的功能化。
General description
1-十六硫醇 (HDT) 在金表面易形成自组装单分子膜 (SAMs)。研究由 HDT 和 3-巯基丙酸组成的二元自组装膜在 Au (111) 表面的相分离特性。利用原子力显微镜 (AFM) 研究金表面与表面活性剂 SAM 之间的相互作用。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Langmuir-Blodgett silver nanowire monolayers for molecular sensing using surface-enhanced Raman spectroscopy.
Tao A, et al.
Nano Letters, 3(9), 1229-1233 (2003)
Lower hole-injection barrier between pentacene and a 1-hexadecanethiol-modified gold substrate with a lowered work function.
Hong K, et al.
Organic Electronics, 9(1), 21-29 (2008)
X Torrelles et al.
Langmuir : the ACS journal of surfaces and colloids, 20(21), 9396-9402 (2004-10-06)
The c(4 x 2) structure of C16H33SH alkanethiol monolayers self-assembled on Au(111) has been studied by grazing incidence X-ray diffraction. This structure coexists on the surface with the (radical3x radical3)R30 degrees phase. The structural refinement of the c(4 x 2)
Jialin Wang et al.
Langmuir : the ACS journal of surfaces and colloids, 24(15), 7889-7896 (2008-06-26)
An atomic force microscope (AFM) was used to measure the forces between gold surfaces with and without hydrophobizing them by the self-assembly of 1-hexadecanethiol. The forces measured between bare gold surfaces were fitted to the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory with a
Catarina Gonçalves et al.
Biomacromolecules, 8(2), 392-398 (2007-02-13)
The amphiphilic molecule dextrin-VA-SC16 (dexC16) was synthesized and studied in this work. DexC16 has a hydrophilic dextrin backbone with grafted acrylate groups (VA) substituted with hydrophobic 1-hexadecanethiol (C16). A versatile synthetic method was developed allowing control of the dextrin degree
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