
4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne | CAS 400775-35-1
Catalog Number | R01-0146 |
Category | Alkynes |
Molecular Formula | C18H30O7 |
Molecular Weight | 358.43 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne is a homobifunctional PEG linker with two propargyl groups. The propargyl group forms triazole linkage with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry.
Chemical Information
Product Specification
Application
Synonyms | Bis-propargyl-PEG7; Bis propargyl-PEG6; Bis[2-[2-[2-(propargyloxy)ethoxy]ethoxy]ethyl] ether |
Purity | >95% |
IUPAC Name | 3-[2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]prop-1-yne |
Canonical SMILES | C#CCOCCOCCOCCOCCOCCOCCOCC#C |
InChI | InChI=1S/C18H30O7/c1-3-5-19-7-9-21-11-13-23-15-17-25-18-16-24-14-12-22-10-8-20-6-4-2/h1-2H,5-18H2 |
InChIKey | WJGHENNJCGFCLO-UHFFFAOYSA-N |
Solubility | Soluble in DMSO |
Density | 1.061±0.06 g/cm3 (Predicted) |
Appearance | Pale Yellow or Colorless Oily Liquid |
Boiling Point | 421.9±40.0 °C at 760 mmHg |
Storage | Store at 2-8°C for short term (days to weeks) or -20°C for long term (months to years) |
1. Biomedical Applications: 4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne is increasingly recognized for its potential in biomedical applications. Its unique structure allows for efficient drug delivery systems, particularly in targeted therapies. The molecule's ability to form stable complexes with various therapeutic agents enhances their solubility and bioavailability. This characteristic is crucial for improving the therapeutic efficacy of drugs, particularly in treating cancer and other chronic diseases, where precise targeting can minimize side effects and maximize treatment effectiveness. Recent studies indicate promising results in using this compound as a carrier for anticancer drugs, paving the way for innovative therapeutic strategies in oncology.
2. Material Science: In material science, 4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne has been explored for its unique physical and chemical properties, making it suitable for the development of advanced materials. Its structural attributes contribute to the creation of novel polymers and composite materials with enhanced mechanical strength and thermal stability. These properties are particularly beneficial in applications such as aerospace and automotive industries, where lightweight yet robust materials are essential. Additionally, the compound's ability to undergo polymerization opens avenues for crafting materials with tailored functionalities, expanding the range of applications in high-performance engineering.
3. Chemical Synthesis: The compound serves as a versatile building block in organic synthesis, facilitating the creation of complex molecules. Its distinct chemical properties allow for various reactions, including cycloadditions and polymerizations, which are fundamental in synthetic organic chemistry. Researchers utilize 4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne to synthesize a range of derivatives that can be employed in pharmaceuticals, agrochemicals, and specialty chemicals. This application underscores its significance in streamlining synthetic pathways and improving the efficiency of chemical processes, ultimately contributing to cost-effective production methods in various industries.
4. Sensor Technology: Another prominent application of 4,7,10,13,16,19,22-Heptaoxapentacosa-1,24-diyne is in the field of sensor technology. Its unique electronic properties make it an excellent candidate for developing advanced sensors, particularly in detecting biomolecules and environmental pollutants. The compound can be integrated into sensor designs to enhance sensitivity and selectivity, crucial for accurate measurements in biomedical diagnostics and environmental monitoring. By leveraging its chemical properties, researchers aim to design next-generation sensors that are more efficient and capable of real-time detection, thereby contributing significantly to public health and environmental safety initiatives.
Recommended Services
Recommended Articles

- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products
Online Inquiry