Cas no 26150-06-1 (3,6,9,12-Tetraoxapentadec-14-en-1-ol)
3,6,9,12-Tetraoxapentadec-14-en-1-ol Chemical and Physical Properties
Names and Identifiers
-
- 3,6,9,12-Tetraoxapentadec-14-en-1-ol
- 2-[2-[2-(2-prop-2-enoxyethoxy)ethoxy]ethoxy]ethanol
- Ethanol,2-[2-[2-[2-(2-propenyloxy)ethoxy]ethoxy]ethoxy]-
- Tetraethylene glycolmonoallyl ether
- 26150-06-1
- 4,7,10,13-Tetraoxa-1-pentadecen-15-ol
- SCHEMBL1115999
- UFTWTGQGRPPFKF-UHFFFAOYSA-N
- AKOS040757902
- HY-138423
- 2-{2-[2-(2-allyloxy-ethoxy)-ethoxy]-ethoxy}-ethanol
- CS-0148253
- 11-Allyloxy-3,6,9-trioxaundecanol
- Acryloyl-PEG4-OH
- DTXSID00435873
- DA-60784
-
- Inchi: 1S/C11H22O5/c1-2-4-13-6-8-15-10-11-16-9-7-14-5-3-12/h2,12H,1,3-11H2
- InChI Key: UFTWTGQGRPPFKF-UHFFFAOYSA-N
- SMILES: O(CCOCCO)CCOCCOCC=C
Computed Properties
- Exact Mass: 234.14676
- Monoisotopic Mass: 234.14672380g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 16
- Rotatable Bond Count: 13
- Complexity: 140
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.5
- Topological Polar Surface Area: 57.2?2
Experimental Properties
- PSA: 57.15
3,6,9,12-Tetraoxapentadec-14-en-1-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | A935952-100mg |
Acryloyl-PEG4-OH |
26150-06-1 | ≥95% | 100mg |
¥1,440.00 | 2022-09-02 |
3,6,9,12-Tetraoxapentadec-14-en-1-ol Related Literature
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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Additional information on 3,6,9,12-Tetraoxapentadec-14-en-1-ol
3,6,9,12-Tetraoxapentadec-14-en-1-ol (CAS No. 26150-06-1): A Versatile Polyether Alcohol for Modern Applications
3,6,9,12-Tetraoxapentadec-14-en-1-ol (CAS No. 26150-06-1) is a unique polyether alcohol compound that has gained significant attention in various industrial and research applications. This oxygen-rich molecule features a distinctive structure with four ether linkages and a terminal hydroxyl group, making it highly valuable for specialized chemical synthesis and formulation processes.
The molecular structure of 3,6,9,12-Tetraoxapentadec-14-en-1-ol consists of a 15-carbon chain containing four evenly spaced oxygen atoms (at positions 3, 6, 9, and 12) and a terminal double bond at the 14-position. This unique arrangement provides both hydrophilic character from the multiple ether groups and reactivity potential from the unsaturated terminal and hydroxyl functionality. Such structural features answer many researchers' questions about "polyethers with dual functionality" or "reactive polyether alcohols."
Recent advancements in green chemistry have highlighted the importance of oxygenated solvents and intermediates like 3,6,9,12-Tetraoxapentadec-14-en-1-ol. Its balanced polarity and relatively low environmental impact make it an attractive alternative to traditional solvents in coatings, adhesives, and specialty cleaning formulations. Industry professionals searching for "eco-friendly polyether alternatives" or "biodegradable chemical intermediates" will find this compound particularly interesting.
In polymer chemistry, 3,6,9,12-Tetraoxapentadec-14-en-1-ol serves as a valuable building block for creating modified polyethers with enhanced properties. The terminal hydroxyl group allows for chain extension or crosslinking, while the double bond offers opportunities for further functionalization through addition reactions. This dual functionality addresses common search queries like "polyethers with reactive end groups" or "versatile ether-based monomers."
The compound's surface-active properties make it useful in specialized surfactant applications where conventional materials may be unsuitable. Its ability to reduce surface tension while maintaining good water solubility has led to investigations in niche areas such as "high-performance wetting agents" and "specialty dispersion aids." These applications align with current market trends toward high-value functional additives.
From a synthetic perspective, 3,6,9,12-Tetraoxapentadec-14-en-1-ol represents an interesting case study in selective etherification techniques. The precise spacing of oxygen atoms in the molecule requires careful control during synthesis, making it relevant to discussions about "controlled oligomerization" and "regioselective ether formation." These topics frequently appear in academic searches related to advanced organic synthesis methods.
In material science applications, researchers have explored 3,6,9,12-Tetraoxapentadec-14-en-1-ol as a modifier for various polymer systems. Its incorporation can influence properties like flexibility, hydrophilicity, and compatibility—key factors for formulators searching for "polymer property modifiers" or "compatibility enhancers." The compound's balanced structure offers unique solutions to common material challenges.
The pharmaceutical and cosmetic industries have shown growing interest in polyether derivatives like 3,6,9,12-Tetraoxapentadec-14-en-1-ol for their potential as penetration enhancers or excipients. While specific applications are still under investigation, the compound's structural features align with current research trends in "transdermal delivery systems" and "novel formulation aids," making it a subject of ongoing study.
Analytical characterization of 3,6,9,12-Tetraoxapentadec-14-en-1-ol presents interesting challenges and opportunities. Modern techniques such as high-resolution mass spectrometry and advanced NMR methods are particularly valuable for confirming its structure and purity. These aspects respond to common analytical chemistry queries about "characterization of complex ethers" or "structural elucidation of polyfunctional compounds."
Market trends indicate increasing demand for specialty polyethers with precise functionality, positioning 3,6,9,12-Tetraoxapentadec-14-en-1-ol as a potentially valuable material. Its combination of ether linkages, hydroxyl group, and unsaturated terminus offers formulators multiple handles for customization—a feature highly sought after in searches for "multifunctional chemical intermediates" and "tailorable polyether compounds."
From a regulatory perspective, 3,6,9,12-Tetraoxapentadec-14-en-1-ol generally falls into favorable categories for industrial use, though specific applications may require additional evaluation. This aspect addresses common industry concerns about "compliant chemical alternatives" and "sustainable material options," particularly in regions with stringent chemical regulations.
Future research directions for 3,6,9,12-Tetraoxapentadec-14-en-1-ol may explore its potential in emerging fields such as bio-based materials or advanced energy applications. The compound's structural versatility makes it a candidate for investigation in areas like "next-generation battery components" or "renewable material platforms," aligning with global sustainability initiatives.
In conclusion, 3,6,9,12-Tetraoxapentadec-14-en-1-ol (CAS No. 26150-06-1) represents a fascinating example of functional polyether chemistry with diverse potential applications. Its unique combination of ether linkages, terminal unsaturation, and hydroxyl functionality provides numerous opportunities for innovation across multiple industries, from advanced materials to specialty formulations. As research continues to uncover new applications, this compound is likely to maintain its relevance in the evolving landscape of specialty chemicals.
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