Tetrahexylammonium Hydroxide

Base Information

• Chemical Name: Tetrahexylammonium Hydroxide
• CAS No.: 17756-56-8
• Molecular Formula: C24H53NO
• Molecular Weight: 371.691
• Hs Code.: 2923900090
• European Community (EC) Number: 629-099-4
• DSSTox Substance ID: DTXSID80553963
• Mol file: 17756-56-8.mol

Synonyms:tetrahexylammonium;tetrahexylammonium benzoate;tetrahexylammonium bromide;tetrahexylammonium chloride;tetrahexylammonium hydroxide;tetrahexylammonium iodide;tetrahexylammonium perchlorate;tetrahexylammonium sulfate (1:1);tetrahexylammonium thicyanate

Chemical Property of Tetrahexylammonium Hydroxide

Chemical Property:

• Refractive Index: n20/D 1.402
• Flash Point: 11 °C
• PSA: 23.06000
• LogP: 7.94760
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 20
• Exact Mass: 371.412715314
• Heavy Atom Count: 26
• Complexity: 195

Purity/Quality:

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

Tetrahexylammonium Hydroxide (10% in Methanol) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C,T,F
• Hazard Codes: C,T,F
• Statements: 34-23/25-11-39/23/24/25-23/24/25
• Safety Statements: 7-16-24-33-45-36/37/39-27-26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC.[OH-]
• Uses: Tetrahexylammonium hydroxide is a phase-transfer reagent that can be used:To synthesize β-D-xyloside- and β-D-xylobioside-based ionic liquids containing tetrahexylammonium cation.As an alkali-free gelling agent to prepare amorphous microporous silica-alumina.To synthesize tetrahexylammonium prolinate, a promising candidate to prepare a solid supported ionic liquid phase (SILP) carbon dioxide absorber.

Technology Process of Tetrahexylammonium Hydroxide

There total 4 articles about Tetrahexylammonium Hydroxide 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:

tetrahexylammonium bromide (4328-13-6) → tetrahexylammonium hydroxide (17756-56-8)

Guidance literature:

With hydroxide-exchange resin; In methanol; water;

DOI:10.1016/j.polymer.2010.11.055

Reference yield:

tetrahexylammonium iodide (2138-24-1) → tetrahexylammonium hydroxide (17756-56-8)

Guidance literature:

With potassium hydroxide; In ethanol; at 60 ℃; for 24h;

Reference yield:

tetra-n-hexylammonium hydrogen sulfate (32503-34-7) → tetrahexylammonium hydroxide (17756-56-8)

Guidance literature:

With sodium hydroxide; In chlorobenzene; Yield given;

DOI:10.1039/c39840001041

upstream raw materials:

tetrahexylammonium chloride

tetra-n-hexylammonium hydrogen sulfate

tetrahexylammonium bromide

tetrahexylammonium iodide

Downstream raw materials:

1-hexene

tri-n-hexylamine

C₈H₇O₃S^(1-)*C₂₄H₅₂N⁽¹⁺⁾

acetylacetone

Refernces

• 1、 Dai, Sheng,Ding, Bingjie,Gong, Xueqing,Hou, Zhenshan,Li, Difan,Tang, Xuan,Xu, Beibei,Yao, Yefeng,Zhang, Tong,Zheng, Anna,Zhou, Qingqing. "Role of Organic Fluoride Salts in Stabilizing Niobium Oxo-Clusters Catalyzing Epoxidation". . p. 8190 - 8203. Retrieved 2021.
• 2、 -. "Novel ionic liquid with peroxyniobate-radical negative ions and preparing method thereof". Page/Page column 7. . Retrieved 2016/12/01.