Dipropylene glycol methyl ether

Base Information

• Chemical Name: Dipropylene glycol methyl ether
• CAS No.: 13588-28-8
• Molecular Formula: C7H16 O3
• Molecular Weight: 148.202
• Hs Code.: 2909499000
• ICSC Number: 0884
• DSSTox Substance ID: DTXSID80864425
• Nikkaji Number: J122.120E
• Wikidata: Q107506664
• Mol file: 13588-28-8.mol

Synonyms:2-(2-methoxypropoxy)propan-1-ol;Dipropylene glycol methyl ether;13588-28-8;2-(2-METHOXYPROPOXY)-1-PROPANOL;1-Propanol, 2-(2-methoxypropoxy)-;2-(2-methoxypropoxy)propanol;12002-25-4;SCHEMBL16073;dipropyleneglycol monomethyl ether;Propanol, oxybis-, methyl ether;DTXSID80864425;AKOS037648698;NCGC00090688-04;BS-15252;LS-62925;CS-0154037;FT-0625302;D81108;J-019668;J-520393;Q2954819

Chemical Property of Dipropylene glycol methyl ether

Chemical Property:

• Boiling Point: 203.3±15.0 °C(Predicted)
• PKA: 14.42±0.10(Predicted)
• PSA: 38.69000
• Density: 0.955±0.06 g/cm3(Predicted)
• LogP: 0.41870
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 148.109944368
• Heavy Atom Count: 10
• Complexity: 75.3

Purity/Quality:

99% ^*data from raw suppliers

2-(2-Methoxypropoxy)propan-1-ol 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Solvents -> Glycol Ethers (P Series)
• Canonical SMILES: CC(CO)OCC(C)OC
• Inhalation Risk: A harmful contamination of the air will be reached rather slowly on evaporation of this substance at 20 °C.
• Effects of Short Term Exposure: The vapour is irritating to the eyes and respiratory tract. The substance may cause effects on the central nervous system. This may result in narcosis.
• Effects of Long Term Exposure: The substance defats the skin, which may cause dryness or cracking.

Technology Process of Dipropylene glycol methyl ether

There total 1 articles about Dipropylene glycol methyl ether 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:

→ di(propylene glycol) monomethyl ether (13588-28-8)

Guidance literature:

Reference yield: 70.0%

di(propylene glycol) monomethyl ether (13588-28-8) + allyl bromide (106-95-6) → di(propylene glycol) allyl methyl ether (68039-31-6)

Guidance literature:

di(propylene glycol) monomethyl ether; With sodium hydride; In tetrahydrofuran;

allyl bromide; In tetrahydrofuran;

DOI:10.1021/jp5072082

Reference yield:

1,4-Dihydroxynaphthalene (571-60-8) + di(propylene glycol) monomethyl ether (13588-28-8) → 1,4-dihydroxy-2-naphthoic acid (31519-22-9)

Guidance literature:

With carbon dioxide; sodium methylate;

Downstream raw materials:

1,4-dihydroxy-2-naphthoic acid

di(propylene glycol) allyl methyl ether

Refernces

• 1、 -. "Methods of alkoxylation". . . Retrieved 2008/06/13.