Cas no 284474-84-6 (Tetra-n-propyl-d28-ammonium Bromide)

Tetra-n-propyl-d28-ammonium Bromide is a deuterated quaternary ammonium compound, where all hydrogen atoms in the propyl chains are replaced by deuterium (d28). This isotopic labeling enhances its utility in NMR spectroscopy, providing sharper signals and reduced background interference due to the absence of proton signals. Its high isotopic purity makes it valuable in mechanistic studies, kinetic isotope effect investigations, and as a reference standard in analytical chemistry. The compound’s stability and well-defined structure further support its use in advanced research applications, particularly in deuterium-labeled synthetic and catalytic processes. Its compatibility with organic solvents ensures versatility in experimental setups.
Tetra-n-propyl-d28-ammonium Bromide structure
284474-84-6 structure
Product Name:Tetra-n-propyl-d28-ammonium Bromide
CAS No:284474-84-6
MF:C12H28BrN
MW:294.433950424194
CID:248476
PubChem ID:16213617
Update Time:2025-05-24

Tetra-n-propyl-d28-ammonium Bromide Chemical and Physical Properties

Names and Identifiers

    • 1-Propan-1,1,2,2,3,3,3-d7-aminium,N,N,N-tri(propyl-d7)-, bromide (9CI)
    • tetrakis(1,1,2,2,3,3,3-heptadeuteriopropyl)azanium,bromide
    • Tetrapropyl-d28 ammonium bromide
    • TETRAPROPYL-D28-AMMONIUM BROMIDE
    • tetrakis(1, 1, 2, 2, 3, 3, 3-heptadeuteriopropyl)azanium;bromide
    • 284474-84-6
    • DTXSID00584072
    • N,N,N-Tris[(~2~H_7_)propyl](~2~H_7_)propan-1-aminium bromide
    • Tetrakis(1,1,2,2,3,3,3-heptadeuteriopropyl)azanium;bromide
    • HY-W096993S
    • CS-0568237
    • F91358
    • Tetrapropyl-d28 ammonium bromide, 98 atom % D
    • Tetra-n-propyl-ammonium-d28 (bromide)
    • Tetra-n-propyl-d28-ammonium Bromide
    • Inchi: 1S/C12H28N.BrH/c1-5-9-13(10-6-2,11-7-3)12-8-4;/h5-12H2,1-4H3;1H/q+1;/p-1/i1D3,2D3,3D3,4D3,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2;
    • InChI Key: BGQMOFGZRJUORO-PJUGJBFXSA-M
    • SMILES: [Br-].[N+](C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])(C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])(C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H]

Computed Properties

  • Exact Mass: 293.31600
  • Monoisotopic Mass: 293.31626g/mol
  • Isotope Atom Count: 28
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 8
  • Complexity: 80.2
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 0?2

Experimental Properties

  • Color/Form: Solids
  • Melting Point: 270?°C (dec.)(lit.)
  • PSA: 0.00000
  • LogP: 0.44720
  • Solubility: Not determined

Tetra-n-propyl-d28-ammonium Bromide Security Information

  • WGK Germany:3
  • Hazard Category Code: 36/37/38
  • Safety Instruction: S26; S36
  • Hazardous Material Identification: Xi
  • Risk Phrases:R36/37/38

Tetra-n-propyl-d28-ammonium Bromide Pricemore >>

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Tetra-n-propyl-d28-ammonium Bromide Related Literature

Additional information on Tetra-n-propyl-d28-ammonium Bromide

Tetra-n-propyl-d28-ammonium Bromide: A Comprehensive Overview

Tetra-n-propyl-d28-ammonium Bromide, with the CAS number 284474-84-6, is a unique compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound, also referred to as Tetra-n-propyl ammonium bromide, is a quaternary ammonium salt with a bromide counterion. Its structure consists of a central nitrogen atom bonded to four n-propyl groups and a bromine atom, making it a highly versatile compound with applications in various scientific domains.

The synthesis of Tetra-n-propyl-d28-ammonium Bromide involves the reaction of n-propyl bromide with an appropriate amine precursor. Recent studies have highlighted the importance of optimizing synthesis conditions to achieve higher yields and purities. For instance, researchers have explored the use of phase-transfer catalysts to enhance the reaction efficiency, which has been particularly beneficial in large-scale production scenarios.

One of the most notable applications of Tetra-n-propyl-d28-ammonium Bromide is in the field of drug delivery systems. The compound's ability to form stable complexes with various bioactive molecules has made it an ideal candidate for encapsulating drugs and delivering them to specific targets within the body. Recent advancements in nanotechnology have further expanded its potential in this area, with researchers developing novel lipid-based nanoparticles that incorporate Tetra-n-propyl-d28-ammonium Bromide as a key component.

In addition to its role in drug delivery, Tetra-n-propyl-d28-ammonium Bromide has also found applications in organic synthesis as a phase-transfer catalyst. Its ability to facilitate reactions between immiscible phases has made it invaluable in the synthesis of complex organic molecules. For example, recent studies have demonstrated its effectiveness in promoting Suzuki-Miyaura couplings, which are widely used in the construction of biaryl compounds with high precision.

The physical properties of Tetra-n-propyl-d28-ammonium Bromide are also worth noting. It is a white crystalline solid with a melting point of approximately 150°C. The compound is soluble in polar solvents such as water and ethanol but exhibits limited solubility in non-polar solvents like hexane. These properties make it suitable for use in various solvent systems, depending on the specific requirements of the application.

From an environmental perspective, Tetra-n-propyl-d28-ammonium Bromide has been shown to exhibit low toxicity towards aquatic organisms, making it a safer alternative to some traditional quaternary ammonium salts. However, further research is needed to fully understand its long-term environmental impact and degradation pathways.

In conclusion, Tetra-n-propyl-d28-ammonium Bromide (CAS No. 284474-84-6) is a multifaceted compound with a wide range of applications across different scientific disciplines. Its unique chemical properties, combined with recent advancements in synthesis and application techniques, position it as a valuable tool for researchers and industry professionals alike. As ongoing studies continue to uncover new potential uses for this compound, its role in scientific innovation is likely to expand even further.

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