Cas no 63893-35-6 (tetra-n-dodecylammonium nitrate)

Tetra-n-dodecylammonium nitrate is a quaternary ammonium salt featuring four long-chain dodecyl groups bonded to a central nitrogen atom, with nitrate as the counterion. This compound is notable for its lipophilic character, making it useful as a phase-transfer catalyst in organic synthesis, particularly for reactions involving immiscible phases. Its high molecular weight and nonpolar alkyl chains enhance solubility in organic solvents, facilitating efficient anion transfer. Additionally, its thermal stability and resistance to hydrolysis under mild conditions make it suitable for applications requiring robust reagents. The nitrate anion further contributes to its reactivity in oxidative or nitration processes. This compound is primarily employed in specialized industrial and research settings.
tetra-n-dodecylammonium nitrate structure
63893-35-6 structure
Product Name:tetra-n-dodecylammonium nitrate
CAS No:63893-35-6
MF:C48H100N+.NO3-
MW:753.3192
CID:961004
PubChem ID:329769515
Update Time:2025-06-07

tetra-n-dodecylammonium nitrate Chemical and Physical Properties

Names and Identifiers

    • tetra-n-dodecylammonium nitrate
    • tetradodecylazanium,nitrate
    • N,N,N-tridodecyldodecan-1-aminium nitrate
    • EINECS 264-548-4
    • tetradodecylazanium;nitrate
    • Tetradodecylammonium nitrate, Selectophore(TM), >=99.0%
    • SCHEMBL3170195
    • NS00087220
    • UNII-801IIU6HOE
    • DTXSID40213516
    • 63893-35-6
    • AHQMUYHFUYRUJV-UHFFFAOYSA-N
    • DTXCID70136007
    • 801IIU6HOE
    • Tetradodecylammonium nitrate
    • 1-DODECANAMINIUM, N,N,N-TRIDODECYL-, NITRATE (1:1) OTHER NAMES
    • MDL: MFCD00467971
    • Inchi: InChI=1S/C48H100N.NO3/c1-5-9-13-17-21-25-29-33-37-41-45-49(46-42-38-34-30-26-22-18-14-10-6-2,47-43-39-35-31-27-23-19-15-11-7-3)48-44-40-36-32-28-24-20-16-12-8-4;2-1(3)4/h5-48H2,1-4H3;/q+1;-1
    • InChI Key: AHQMUYHFUYRUJV-UHFFFAOYSA-N
    • SMILES: CCCCCCCCCCCC[N+](CCCCCCCCCCCC)(CCCCCCCCCCCC)CCCCCCCCCCCC.[N+](=O)([O-])[O-]

Computed Properties

  • Exact Mass: 752.7739
  • Monoisotopic Mass: 752.77339506g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 53
  • Rotatable Bond Count: 44
  • Complexity: 487
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 62.9?2

Experimental Properties

  • Melting Point: 103-105?°C
  • PSA: 66.2

tetra-n-dodecylammonium nitrate Security Information

  • Symbol: GHS02 GHS07
  • Signal Word:Warning
  • Hazard Statement: H228-H315-H319-H335
  • Warning Statement: P210-P261-P305+P351+P338
  • Hazardous Material transportation number:UN 1325 4.1/PG 3
  • WGK Germany:3
  • Hazard Category Code: 11-36/37/38
  • Safety Instruction: 26-36
  • Hazardous Material Identification: Xi
  • Risk Phrases:R36/37/38;R8
  • Safety Term:S17;S26;S36

tetra-n-dodecylammonium nitrate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd.
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tetra-n-dodecylammonium nitrate
63893-35-6 99.0%
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Additional information on tetra-n-dodecylammonium nitrate

Properties and Applications of Tetra-n-dodecylammonium Nitrate (CAS No 63893-35-6)

Tetra-n-dodecylammonium nitrate, with the chemical formula C24H51NO4 and CAS number 63893-35-6, is a quaternary ammonium salt that has garnered significant attention in various scientific and industrial applications. This compound, characterized by its long alkyl chains and nitrate counterion, exhibits unique physicochemical properties that make it valuable in multiple domains, including catalysis, material science, and environmental remediation.

The structure of tetra-n-dodecylammonium nitrate consists of a central nitrogen atom coordinated to four dodecyl groups (C12H25), which are hydrophobic in nature. The nitrate anion (NO3-) provides ionic character to the compound, facilitating its solubility in polar solvents. This balance between hydrophobic and hydrophilic regions makes it an excellent surfactant and phase-transfer catalyst, enabling the facilitation of reactions between immiscible phases.

Recent research has highlighted the role of tetra-n-dodecylammonium nitrate in catalytic systems. Its ability to stabilize reactive intermediates and enhance reaction rates has been observed in various organic transformations. For instance, studies have demonstrated its effectiveness in promoting the coupling reactions of aldehydes and ketones under mild conditions, which is particularly relevant in the synthesis of fine chemicals and pharmaceuticals. The long alkyl chains not only improve the compound's solubility in organic media but also enhance its surface activity, making it suitable for use as an emulsifier and demulsifier.

In material science, tetra-n-dodecylammonium nitrate has been explored for its potential in the formation of liquid crystals and as a modifier for polymer matrices. Its structural properties allow it to align in specific orientations, which can be exploited to create materials with tailored optical and electrical properties. Additionally, its compatibility with various polymers has led to its use in enhancing the mechanical strength and thermal stability of composite materials.

The environmental applications of tetra-n-dodecylammonium nitrate are also noteworthy. Its surfactant properties have been leveraged in the development of efficient cleaning agents and detergents. Furthermore, research suggests that it can be used as a coagulant in water treatment processes, aiding in the removal of suspended particles and organic contaminants. The compound's biodegradability and low toxicity profile make it an attractive option for environmentally friendly formulations.

From a pharmaceutical perspective, tetra-n-dodecylammonium nitrate has shown promise as a component in drug delivery systems. Its ability to form stable complexes with hydrophobic drugs enhances their solubility and bioavailability. This property is particularly valuable in the development of oral formulations where poor solubility often limits therapeutic efficacy. Additionally, its antimicrobial properties have been investigated for potential applications in wound care and antimicrobial coatings.

The industrial significance of tetra-n-dodecylammonium nitrate extends to its role as a flame retardant additive. When incorporated into polymers and other materials, it can improve fire resistance by releasing water vapor or char-forming compounds during combustion. This application is critical in enhancing the safety of consumer products, building materials, and transportation systems.

Advances in nanotechnology have also opened new avenues for the use of tetra-n-dodecylammonium nitrate. Its ability to stabilize nanoparticles has been utilized to create colloidal suspensions with controlled particle size distribution. These suspensions are essential for various nanotechnology applications, including electronics, coatings, and biomedical devices.

The synthesis of tetra-n-dodecylammonium nitrate typically involves the reaction of dodecyldimethylamine with nitric acid under controlled conditions. Recent improvements in synthetic methodologies have focused on optimizing yield and purity while minimizing environmental impact. Green chemistry principles have been applied to develop more sustainable production processes, such as using bio-based feedstocks or catalytic methods that reduce waste generation.

The future prospects for tetra-n-dodecylammonium nitrate are promising, with ongoing research exploring new applications and refining existing ones. As scientific understanding advances, novel uses are likely to emerge across multiple industries. The compound's versatility and well-characterized properties ensure that it will remain a valuable asset in both academic research and industrial development.

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