
Propynol ethoxylate | CAS 3973-18-0
| Catalog Number | R01-0194 |
| Category | Alkynes |
| Molecular Formula | C5H8O2 |
| Molecular Weight | 100.12 |
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Product Introduction
2-(2-Propyn-1-yloxy)ethanol (CAS# 3973-18-0) is an intermediate and it is shown to be used in the design and synthesis of a tag-free chemical probe for photoafiinity labeling.
Chemical Information
Product Specification
Application
Chemical Information
| Related CAS | 32199-97-6 (polymer) |
| Synonyms | Propargyl-PEG2-alcohol; Propargyl-PEG1-alcohol; 2-(2-Propyn-1-yloxy)ethanol; 2-(2-Propynyloxy)ethanol; 2-Propynoxyethanol; 3-(2-Hydroxyethoxy)-1-propyne; 4-Oxa-1-hexyn-6-ol; Ethylene Glycol Monopropargyl Ether; Ethanol, 2-(2-propynyloxy)- |
| Purity | >97% |
| IUPAC Name | 2-prop-2-ynoxyethanol |
| SMILES | C#CCOCCO |
| InChI | InChI=1S/C5H8O2/c1-2-4-7-5-3-6/h1,6H,3-5H2 |
| InChIKey | GHGCQQRMJCSIBQ-UHFFFAOYSA-N |
| Solubility | Soluble in Chloroform (Sparingly), Ethyl Acetate (Slightly) |
| Density | 1.0261 g/cm3 |
| Appearance | Pale Yellow or Colorless Oily Matter |
| Boiling Point | 80-90°C at 12-14 Torr |
| LogP | -0.37150 |
Product Specification
| Storage | Store at 2-8°C |
| Signal | Danger |
| Precautionary Statement Codes | P203, P260, P261, P264, P264+P265, P270, P271, P280, P284, P301+P317, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P318, P319, P320, P330, P337+P317, P403+P233, P405, and P501 |
Application
Propynol ethoxylate is a nonionic alkyne-bearing surfactant designed for click-chemistry workflows that benefit from water-compatible handling and controlled surface activity. As an alkyne functionalized reagent, it is commonly used as a building block for copper-catalyzed azide–alkyne cycloaddition (CuAAC) and related alkyne click formats, enabling attachment of azide-tagged motifs to surfaces, nanoparticles, and polymeric assemblies. Its ethoxylated structure provides solubilization and interfacial compatibility, making it attractive for preparing functional materials and probe platforms where homogeneous dispersion and reproducible conjugation are important.
1. Surface Functionalization
Propynol ethoxylate is frequently used to introduce clickable alkyne functionality onto substrates and interfaces in materials science workflows. Researchers incorporate it into coating formulations, surface modification steps, or interfacial layers to enable subsequent coupling with azide-bearing ligands, dyes, or affinity tags. The ethoxylated, nonionic character helps maintain wetting and processability across diverse surface chemistries, supporting consistent functional density when preparing clickable surfaces for downstream assays, imaging experiments, or materials characterization.
2. Polymer and Hydrogel Labeling
Propynol ethoxylate serves as a practical alkyne component for labeling polymer networks and hydrogel systems that require compatibility with aqueous processing. In chemical biology and biomaterials research, it is used to install alkyne handles into polymerizable or blendable formulations so that azide-functional probes can be attached post-fabrication. This approach supports modular probe exchange and spatially defined labeling strategies, including preparation of clickable hydrogels for studying material–molecule interactions, diffusion behavior, and surface-dependent binding of tagged reagents.
3. Nanoparticle Conjugation
Propynol ethoxylate is used in nanoparticle and colloidal conjugation workflows where a water-compatible clickable surfactant helps control dispersion and presentation of reactive groups. By providing alkyne functionality in a form that can associate with or be incorporated into colloidal systems, it enables coupling to azide-functional targeting moieties, fluorescent reporters, or analytical tags. This use case is common in materials and imaging tool development, where reproducible surface coverage and stable colloidal behavior are essential for consistent probe performance across experimental batches.
4. Reagent and Probe Platforms
Propynol ethoxylate is also applied as a functional handle in the preparation of click-ready reagent and probe platforms used across chemical biology and molecular imaging research. Its alkyne functionality supports rapid assembly of azide-functional components into multivalent constructs, including fluorescent or affinity-tagged reporters used for labeling, tracking, and material interrogation. The surfactant-like ethoxylate scaffold is particularly valued when probe formulations must remain manageable in aqueous media while still enabling efficient downstream click conjugation to azide-bearing partners.
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