1-Octanethiol

Standard for GC, ≥99.6%(GC)

Reagent Code: #220922
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CAS Number 111-88-6

science Other reagents with same CAS 111-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.29 g/mol
Formula C₈H₁₈S
badge Registry Numbers
EC Number 203-918-1
MDL Number MFCD00004912
thermostat Physical Properties
Melting Point -49 °C
Boiling Point 197-200 °C(lit.)
inventory_2 Storage & Handling
Density 0.843 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a surface modifier in nanotechnology, particularly for stabilizing gold nanoparticles due to its thiol group binding strongly to metal surfaces. Acts as a capping agent in the synthesis of quantum dots and other nanomaterials, controlling particle growth and preventing aggregation. Employed in self-assembled monolayers (SAMs) for creating hydrophobic surfaces and in sensor development where surface functionalization is critical. Also utilized in organic synthesis as a protecting group or intermediate in the preparation of sulfides and other sulfur-containing compounds. Its long hydrocarbon chain contributes to low water solubility and high affinity for nonpolar environments, making it useful in phase transfer applications and interfacial chemistry.

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inventory 5ml
10-20 days ฿980.00

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1-Octanethiol
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Used as a surface modifier in nanotechnology, particularly for stabilizing gold nanoparticles due to its thiol group binding strongly to metal surfaces. Acts as a capping agent in the synthesis of quantum dots and other nanomaterials, controlling particle growth and preventing aggregation. Employed in self-assembled monolayers (SAMs) for creating hydrophobic surfaces and in sensor development where surface functionalization is critical. Also utilized in organic synthesis as a protecting group or intermed

Used as a surface modifier in nanotechnology, particularly for stabilizing gold nanoparticles due to its thiol group binding strongly to metal surfaces. Acts as a capping agent in the synthesis of quantum dots and other nanomaterials, controlling particle growth and preventing aggregation. Employed in self-assembled monolayers (SAMs) for creating hydrophobic surfaces and in sensor development where surface functionalization is critical. Also utilized in organic synthesis as a protecting group or intermediate in the preparation of sulfides and other sulfur-containing compounds. Its long hydrocarbon chain contributes to low water solubility and high affinity for nonpolar environments, making it useful in phase transfer applications and interfacial chemistry.

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