3-(prop-2-ynyloxy)propanoic acid

≥95%

Reagent Code: #224931
label
Alias Propargyl-PEG1-acid
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CAS Number 55683-37-9

science Other reagents with same CAS 55683-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.13 g/mol
Formula C₆H₈O₃
badge Registry Numbers
MDL Number MFCD10689189
thermostat Physical Properties
Boiling Point 265.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and bioconjugation applications. Also employed in the development of functional polymers and coatings due to its ability to undergo cross-linking reactions. Its carboxylic acid group facilitates derivatization into esters, amides, and other derivatives for tailored molecular design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿5,720.00
inventory 5g
10-20 days ฿25,560.00
inventory 250mg
10-20 days ฿2,110.00

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3-(prop-2-ynyloxy)propanoic acid
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and bioconjugation applications. Also employed in the development of functional polymers and coatings due to its ability to undergo cross-linking reactions. Its carboxylic acid group facilitates derivatiz

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in drug discovery and bioconjugation applications. Also employed in the development of functional polymers and coatings due to its ability to undergo cross-linking reactions. Its carboxylic acid group facilitates derivatization into esters, amides, and other derivatives for tailored molecular design.

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