CID 520163

Base Information

• Chemical Name: CID 520163
• CAS No.: 2498-20-6
• Molecular Formula: C20H44IN
• Molecular Weight: 425.481
• Hs Code.: 2923900090
• Mol file: 2498-20-6.mol

Synonyms:

Chemical Property of CID 520163

Chemical Property:

• Appearance/Colour: Liquid
• Melting Point: 134-137 °C

• PSA: 0.00000
• LogP: 3.56800
• Storage Temp.: Store below +30°C.
• Sensitive.: Light Sensitive
• Solubility.: 7.40g/l
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 425.25185
• Heavy Atom Count: 22
• Complexity: 160

Purity/Quality:

98%,99%, ^*data from raw suppliers

Tetraamylammonium Iodide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC[N+](CCCCC)(CCCCC)CCCCC.[I-]
• Uses: Tetraamylammonium Iodide is is a quaternary ammonium based antimicrobial used as a bacteriostat, deodorant, disinfectant and(or) a microbiocide.

Technology Process of CID 520163

There total 2 articles about CID 520163 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

amyl iodide (628-17-1) + tripentylamine (621-77-2) → tetrapentylammonium iodide (2498-20-6)

Guidance literature:

at 70 ℃;

DOI:10.1021/ja01264a030

Reference yield:

→ tetrapentylammonium iodide (2498-20-6)

Guidance literature:

Tri-n-amyl-amin, 1-Iodpentan/Me./Rueckfluss/ 36 h;

DOI:10.1021/ja01462a011

Reference yield:

tetrapentylammonium iodide (2498-20-6) → tetrapentylammonium bromide (866-97-7)

Guidance literature:

With ammonium bromide; In dichloromethane; water;

DOI:10.1021/acs.cgd.5b01342

upstream raw materials:

amyl iodide

tripentylamine

Downstream raw materials:

C₂₀H₄₄N⁽¹⁺⁾*C₁₅H₁₀N₃O₃^(1-)

[(C₅H₁₁)4N]⁽¹⁺⁾*[(C₆H₅)3Sn(OCOCF₃)I]^(1-) = [(C₅H₁₁)4N][(C₆H₅)3Sn(OCOCF₃)I]

tetrapentylammonium bromide