2,4,6,8-Tetraoxanonane

Base Information

• Chemical Name: 2,4,6,8-Tetraoxanonane
• CAS No.: 13353-03-2
• Molecular Formula: C5H12O4
• Molecular Weight: 136.148
• European Community (EC) Number: 818-232-3
• DSSTox Substance ID: DTXSID60709264
• Nikkaji Number: J1.171.940F
• Mol file: 13353-03-2.mol

Synonyms:2,4,6,8-Tetraoxanonane;13353-03-2;methoxy(methoxymethoxymethoxy)methane;SCHEMBL13947195;DTXSID60709264;MFCD26792354;AKOS024463664;AS-40337;CS-0186491

Chemical Property of 2,4,6,8-Tetraoxanonane

Chemical Property:

• Melting Point: -42--40.5 °C
• Boiling Point: 158-159℃
• PSA: 36.92000
• Density: 1.0242 g/cm3(Temp: 25 °C)
• LogP: 0.18490
• Storage Temp.: 2-8°C
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 136.07355886
• Heavy Atom Count: 9
• Complexity: 42.2

Purity/Quality:

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

2,4,6,8-Tetraoxanonane 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COCOCOCOC
• Use Description: 2,4,6,8-Tetraoxanonane, a specific chemical compound, serves distinct functions across various fields. In the pharmaceutical sector, it may be utilized as a potential building block for the synthesis of compounds with desired properties, contributing to drug discovery and development. In organic synthesis, this compound can play a role as a versatile reagent, enabling the creation of complex molecular structures for various applications. Additionally, in the realm of polymer science, it could be employed as a precursor in the production of specialized polymers or materials. Its applications in pharmaceuticals, organic synthesis, and materials science underscore its significance in driving innovation, scientific exploration, and practical solutions within these diverse domains.

Technology Process of 2,4,6,8-Tetraoxanonane

There total 28 articles about 2,4,6,8-Tetraoxanonane 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: 22.4%

formaldehyd (50-00-0,30525-89-4,61233-19-0) + Dimethoxymethane (109-87-5) → bis-methoxymethoxy-methane (13353-03-2) + bis(methoxymethyl)ether (628-90-0) + POMM4 (13352-75-5)

Guidance literature:

With La₂O₃ doped titania; at 130 ℃; for 4h; under 4500.45 Torr; Reagent/catalyst; Pressure; Autoclave;

Reference yield: 16.7%

methanol (67-56-1) + formaldehyd (50-00-0,30525-89-4,61233-19-0) → bis-methoxymethoxy-methane (13353-03-2) + bis(methoxymethyl)ether (628-90-0)

Guidance literature:

With ZrO₂#dotLa₂O₃; at 130 ℃; for 4h; under 5250.53 Torr;

Reference yield:

methanol (67-56-1) + formaldehyd (50-00-0,30525-89-4,61233-19-0) + Dimethoxymethane (109-87-5) → bis-methoxymethoxy-methane (13353-03-2)

Guidance literature:

With sulfuric acid;

upstream raw materials:

methanol

formaldehyd

Dimethoxymethane

sulfuric acid

Downstream raw materials:

Bis(2-hydroxyphenyl)methane

2-[(4-hydroxyphenyl)methyl]phenol

bis-(4-hydroxyphenyl)methane

Refernces

• 1、 -. "Novel synthesis method of alkoxymethylamine compound". Paragraph 0059; 0060. . Retrieved 2019/10/01.
• 2、 Song, Yu-He,Hou, Xing-Ming,Song, Juan,Zhang, Yue,Wang, Jie,Wei, Ping-He,Li, Cun-Fu. "Three Binary Azeotropic Systems for 1-(Methoxymethoxy)-propane, 1-(Ethoxymethoxy)-propane, and Methoxy(methoxymethoxy)methane with Three Alcohols at 101.33 kPa: Experimental Data, Correlation, and Purification". . p. 138 - 146. Retrieved 2018/01/18.