Cas no 61188-11-2 (4,7,10-Tridecatrien-1-ol, acetate)
4,7,10-Tridecatrien-1-ol, acetate Chemical and Physical Properties
Names and Identifiers
-
- 4,7,10-Tridecatrien-1-ol, acetate
- acetic acid,trideca-4,7,10-trien-1-ol
- acetic acid;trideca-4,7,10-trien-1-ol
- 61188-11-2
-
- Inchi: 1S/C13H22O.C2H4O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14;1-2(3)4/h3-4,6-7,9-10,14H,2,5,8,11-13H2,1H3;1H3,(H,3,4)
- InChI Key: UATGTTMKOCJRRX-UHFFFAOYSA-N
- SMILES: OCCCC=CCC=CCC=CCC.OC(C)=O
Computed Properties
- Exact Mass: 254.18828
- Monoisotopic Mass: 254.18819469g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 18
- Rotatable Bond Count: 8
- Complexity: 209
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 3
- Topological Polar Surface Area: 57.5?2
Experimental Properties
- PSA: 57.53
4,7,10-Tridecatrien-1-ol, acetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T611880-1mg |
4,7,10-Tridecatrien-1-ol, Acetate |
61188-11-2 | 1mg |
$190.00 | 2023-05-17 | ||
| TRC | T611880-10mg |
4,7,10-Tridecatrien-1-ol, Acetate |
61188-11-2 | 10mg |
$1499.00 | 2023-05-17 |
4,7,10-Tridecatrien-1-ol, acetate Related Literature
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Robert J. Meagher,Anson V. Hatch,Ronald F. Renzi,Anup K. Singh Lab Chip, 2008,8, 2046-2053
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Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
Additional information on 4,7,10-Tridecatrien-1-ol, acetate
4,7,10-Tridecatrien-1-ol, Acetate (CAS No: 61188-11-2)
The compound 4,7,10-Tridecatrien-1-ol, Acetate (CAS No: 61188-11-2) is a fascinating molecule with significant applications in various fields. This compound belongs to the class of esters and is derived from the reaction of 4,7,10-tridecatrien-1-ol with acetic acid. Its chemical structure consists of a tridecatriene backbone with hydroxyl and acetate groups at specific positions. The presence of multiple double bonds in the carbon chain imparts unique physical and chemical properties to this compound.
Recent studies have highlighted the importance of 4,7,10-Tridecatrien-1-ol, Acetate in the field of materials science. Researchers have explored its potential as a precursor for synthesizing advanced polymers and biomaterials. The compound's ability to undergo various polymerization reactions has made it a valuable building block in the development of high-performance materials. For instance, its use in creating biodegradable polymers has gained traction due to increasing environmental concerns.
In addition to its role in materials science, 4,7,10-Tridecatrien-1-ol, Acetate has also found applications in the fragrance and flavor industries. Its distinct aroma profile makes it an ideal ingredient in perfumes and cosmetic products. The compound's stability under various environmental conditions ensures that it retains its fragrance properties over extended periods. This attribute has made it a preferred choice for manufacturers seeking long-lasting scent solutions.
The synthesis of 4,7,10-Tridecatrien-1-ol, Acetate involves a multi-step process that requires precise control over reaction conditions. Recent advancements in catalytic methods have improved the efficiency and yield of this synthesis process. For example, the use of transition metal catalysts has enabled researchers to achieve higher purity levels while minimizing by-products. These improvements have significantly reduced production costs and enhanced the scalability of the process.
Another area where 4,7,10-Tridecatrien-1-ol, Acetate has shown promise is in biomedical applications. Studies have demonstrated its potential as a drug delivery agent due to its biocompatible nature and ability to encapsulate hydrophobic drugs. The compound's ability to form stable emulsions has made it a candidate for targeted drug delivery systems. Furthermore, its biodegradability ensures that it does not pose long-term risks to biological systems.
The compound's physical properties also make it suitable for use in lubricants and industrial oils. Its high viscosity index and thermal stability allow it to function effectively under extreme conditions. Recent research has focused on optimizing its formulation for use in high-performance lubricants used in aerospace and automotive industries.
In conclusion, 4,7,10-Tridecatrien-1-ol, Acetate (CAS No: 61188-11-2) is a versatile compound with diverse applications across multiple industries. Its unique chemical structure and favorable physical properties make it an invaluable resource for scientists and engineers alike. As research continues to uncover new potential uses for this compound, its significance in various fields is expected to grow further.
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