Cas no 161838-87-5 (1,1,1-Trimethoxyoctane)

1,1,1-Trimethoxyoctane is a branched alkoxy compound characterized by its three methoxy groups attached to a central carbon atom within an octane framework. This structure imparts unique reactivity, making it a valuable intermediate in organic synthesis, particularly in the formation of acetals and other protective groups. Its stability under neutral conditions and controlled reactivity under acidic or basic conditions enhance its utility in fine chemical and pharmaceutical applications. The compound’s hydrophobic nature also lends itself to use in specialty formulations requiring solubility in nonpolar solvents. Careful handling is advised due to potential sensitivity to moisture and strong acids or bases.
1,1,1-Trimethoxyoctane structure
1,1,1-Trimethoxyoctane structure
Product Name:1,1,1-Trimethoxyoctane
CAS No:161838-87-5
MF:C11H24O3
MW:204.306464195251
CID:1063113
PubChem ID:15643673
Update Time:2025-05-21

1,1,1-Trimethoxyoctane Chemical and Physical Properties

Names and Identifiers

    • 1,1,1-Trimethoxyoctane
    • 1,1,1-Trimethoxyocta
    • 1,1,1- trimethoxy ocatane
    • 161838-87-5
    • DB-259019
    • 1,1,1-Trimethoxy-n-octane
    • SAEZBIIRXDZCAB-UHFFFAOYSA-N
    • SCHEMBL11253869
    • trimethyl orthooctanoate
    • EX-A8306
    • Inchi: 1S/C11H24O3/c1-5-6-7-8-9-10-11(12-2,13-3)14-4/h5-10H2,1-4H3
    • InChI Key: SAEZBIIRXDZCAB-UHFFFAOYSA-N
    • SMILES: O(C)C(CCCCCCC)(OC)OC

Computed Properties

  • Exact Mass: 204.17254462g/mol
  • Monoisotopic Mass: 204.17254462g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 9
  • Complexity: 113
  • 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: 3.3
  • Topological Polar Surface Area: 27.7?2

1,1,1-Trimethoxyoctane Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
T795725-100mg
1,1,1-Trimethoxyoctane
161838-87-5
100mg
$ 161.00 2023-09-05
TRC
T795725-500mg
1,1,1-Trimethoxyoctane
161838-87-5
500mg
$ 666.00 2023-09-05
TRC
T795725-1g
1,1,1-Trimethoxyoctane
161838-87-5
1g
$ 1288.00 2023-09-05
TRC
T795725-1000mg
1,1,1-Trimethoxyoctane
161838-87-5
1g
$1286.00 2023-05-17

Additional information on 1,1,1-Trimethoxyoctane

1,1,1-Trimethoxyoctane: A Comprehensive Overview

1,1,1-Trimethoxyoctane (CAS No. 161838-87-5) is a versatile organic compound that has garnered significant attention in various industrial and research domains. This compound is characterized by its unique structure, which consists of an octane backbone with three methoxy groups attached to the first carbon atom. The presence of these methoxy groups imparts distinctive chemical properties, making 1,1,1-trimethoxyoctane a valuable material in numerous applications.

Recent studies have highlighted the potential of trimethoxyoctane derivatives in the field of polymer chemistry. Researchers have explored the use of trimethoxyoctane-based polymers in the development of advanced materials for electronic devices. These polymers exhibit excellent thermal stability and mechanical properties, making them suitable for high-performance applications such as flexible electronics and optoelectronic devices. The ability of trimethoxyoctane to form stable polymer networks has been a focal point in recent research, with findings published in leading journals like *Macromolecules* and *Polymer Chemistry*.

In addition to its role in polymer science, trimethoxyoctane has also been investigated for its potential in pharmaceutical applications. The compound's structure allows for easy functionalization, enabling the creation of bioactive molecules with tailored pharmacokinetic properties. A 2023 study published in *Journal of Medicinal Chemistry* demonstrated that trimethoxyoctane derivatives could serve as promising candidates for drug delivery systems due to their ability to enhance drug solubility and bioavailability.

The synthesis of trimethoxyoctane typically involves a multi-step process that includes alkylation and methylation reactions. Recent advancements in catalytic methods have significantly improved the efficiency of these reactions. For instance, the use of palladium-catalyzed cross-coupling reactions has enabled the selective synthesis of trimethoxyoctane derivatives with high purity and yield. These developments have been widely reported in scientific literature, underscoring the importance of optimizing synthetic pathways for industrial-scale production.

From an environmental perspective, the biodegradability and toxicity of trimethoxyoctane have been extensively studied. Research indicates that the compound exhibits moderate biodegradability under aerobic conditions, making it less persistent in aquatic environments compared to other organics. However, further studies are required to fully understand its long-term ecological impact. Regulatory agencies such as the U.S. Environmental Protection Agency (EPA) have expressed interest in these findings, particularly in relation to industrial waste management practices.

The application of trimethoxyoctane extends beyond traditional chemical industries. Recent breakthroughs have explored its use in renewable energy technologies, such as lithium-ion batteries and fuel cells. For example, a 2023 study published in *Energy & Environmental Science* demonstrated that trimethoxyoctane-based electrolytes could significantly enhance battery performance by improving ion conductivity and reducing resistance. This discovery has opened new avenues for sustainable energy storage solutions.

In conclusion, trimethoxyoctane (CAS No. 161838-87-5) is a multifaceted compound with a wide range of applications across diverse fields. Its unique chemical properties and versatility make it an invaluable resource for researchers and industry professionals alike. As ongoing studies continue to uncover new potential uses for this compound, it is poised to play an increasingly important role in advancing technological innovation and sustainable practices.

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