1-Hexadecyne

90%(GC)

Reagent Code: #195057
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CAS Number 629-74-3

science Other reagents with same CAS 629-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.42 g/mol
Formula C₁₆H₃₀
badge Registry Numbers
MDL Number MFCD00015084
thermostat Physical Properties
Melting Point 13°C(凝固点)
Boiling Point 284°C(lit.)
inventory_2 Storage & Handling
Density 0.8
Storage Room temperature, dry

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of long-chain alkynes and functionalized hydrocarbons. It serves as a reagent in coupling reactions, including Sonogashira and Glaser couplings, to construct carbon-carbon bonds in pharmaceuticals and agrochemicals. Also employed in surface modification processes, where it can form self-assembled monolayers on metal surfaces, providing hydrophobic coatings or corrosion resistance. Its terminal alkyne group enables click chemistry applications, useful in material science and polymer modification. Additionally, it acts as a precursor in the synthesis of surfactants, lubricants, and specialty chemicals requiring extended hydrophobic chains.

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Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿1,880.00
inventory 5ml
10-20 days ฿7,680.00
inventory 25ml
10-20 days ฿21,050.00

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1-Hexadecyne
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Used as a building block in organic synthesis, particularly in the preparation of long-chain alkynes and functionalized hydrocarbons. It serves as a reagent in coupling reactions, including Sonogashira and Glaser couplings, to construct carbon-carbon bonds in pharmaceuticals and agrochemicals. Also employed in surface modification processes, where it can form self-assembled monolayers on metal surfaces, providing hydrophobic coatings or corrosion resistance. Its terminal alkyne group enables click chemis

Used as a building block in organic synthesis, particularly in the preparation of long-chain alkynes and functionalized hydrocarbons. It serves as a reagent in coupling reactions, including Sonogashira and Glaser couplings, to construct carbon-carbon bonds in pharmaceuticals and agrochemicals. Also employed in surface modification processes, where it can form self-assembled monolayers on metal surfaces, providing hydrophobic coatings or corrosion resistance. Its terminal alkyne group enables click chemistry applications, useful in material science and polymer modification. Additionally, it acts as a precursor in the synthesis of surfactants, lubricants, and specialty chemicals requiring extended hydrophobic chains.

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