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H12005

Sigma-Aldrich

1,6-Hexanedithiol

96%

Synonym(s):

1,6-Dimercaptohexane, DMH, Hexamethylene dimercaptan

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About This Item

Linear Formula:
HS(CH2)6SH
CAS Number:
Molecular Weight:
150.31
Beilstein:
1732507
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

~1 mmHg ( 20 °C)

Assay

96%

form

liquid

refractive index

n20/D 1.511 (lit.)

bp

118-119 °C/15 mmHg (lit.)

mp

−21 °C (lit.)

density

0.983 g/mL at 25 °C (lit.)

SMILES string

SCCCCCCS

InChI

1S/C6H14S2/c7-5-3-1-2-4-6-8/h7-8H,1-6H2

InChI key

SRZXCOWFGPICGA-UHFFFAOYSA-N

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General description

1,6-Hexanedithiol (HDT) is a long chained bi-functional alkanethiol with 6 carbon atoms structured in a zig-zag pattern, which forms a tetrahedral configuration. It is mainly used as a self-assembled monolayer (SAM) as it functionalizes various surfaces and immobilizes a variety of nanomaterials.

Application

HDT can be used to functionalize molybdenum disulphide (MoS2), which can be used as a two dimensional transition metal dichalcogenide (TMD) in electronics and optoelectronic devices. It forms a SAM on gallium arsenic (GaAs) doped cadmium sulfide (CdS) quantum dots (QDs), which can be used for biosensors and solar applications. It can also be used to immobilize gold nanoparticles (AuNPs) for potential usage in biomedical and bioanalytical applications.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Theoretical and experimental investigation of conjugation of 1, 6-hexanedithiol on MoS2.
Gul A, et al.
Materials Research Express, 5(3), 036415-036415 (2018)
Investigation of biocatalytic enlargement of gold nanoparticles using dynamic light scattering and atomic force microscopy.
Ramanaviciene A, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 510(4), 183-189 (2016)
Thin film fabrication of CdS quantum dots on GaAs substrate by surfactant self-assembly.
Park S and Kongb H
Journal of Ceramic Processing Research, 19(4), 337-341 (2018)
Haixing Li et al.
Journal of the American Chemical Society, 137(15), 5028-5033 (2015-02-13)
Here we study the stability and rupture of molecular junctions under high voltage bias at the single molecule/single bond level using the scanning tunneling microscope-based break-junction technique. We synthesize carbon-, silicon-, and germanium-based molecular wires terminated by aurophilic linker groups
Lianfang Chen et al.
Journal of chromatography. A, 1394, 103-110 (2015-04-09)
A novel organic monolith was firstly prepared in a UV-transparent fused-silica capillary by a single-step approach via photo-initiated thiol-ene click polymerization reaction of 1,2,4-trivinylcyclohexane (TVCH) and pentaerythriol tetra(3-mercaptopropionate) (4SH) within 10min. The effects of both composition of prepolymerization solution and

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