Myristic Acid Alkyne

98%

Reagent Code: #108986
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CAS Number 82909-47-5

science Other reagents with same CAS 82909-47-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.3 g/mol
Formula C₁₄H₂₄O₂
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

Myristic Acid Alkyne is widely used in the field of organic synthesis and material science. Its alkyne functional group makes it a valuable building block for click chemistry, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. This compound is also employed in the development of advanced materials, such as polymers and dendrimers, where its hydrophobic tail and reactive alkyne group enable precise modifications and functionalization. Additionally, it finds applications in bioconjugation techniques, where it is used to attach biomolecules like proteins or peptides to surfaces or other molecules for research and diagnostic purposes. Its role in lipid research is also notable, as it serves as a model compound for studying lipid interactions and membrane dynamics.

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Test Parameter Specification
Appearance Off-White Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500μg
10-20 days ฿47,025.00

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Myristic Acid Alkyne
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Myristic Acid Alkyne is widely used in the field of organic synthesis and material science. Its alkyne functional group makes it a valuable building block for click chemistry, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. This compound is also employed in the development of advanced materials, such as polymers and dendrimers, where its hydrophobic tail and reactive alkyne group enable precise modifications and functionalization.

Myristic Acid Alkyne is widely used in the field of organic synthesis and material science. Its alkyne functional group makes it a valuable building block for click chemistry, particularly in the synthesis of complex molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. This compound is also employed in the development of advanced materials, such as polymers and dendrimers, where its hydrophobic tail and reactive alkyne group enable precise modifications and functionalization. Additionally, it finds applications in bioconjugation techniques, where it is used to attach biomolecules like proteins or peptides to surfaces or other molecules for research and diagnostic purposes. Its role in lipid research is also notable, as it serves as a model compound for studying lipid interactions and membrane dynamics.

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