Tripropylene glycol mono-n-butyl ether

Base Information

• Chemical Name: Tripropylene glycol mono-n-butyl ether
• CAS No.: 57499-93-1
• Molecular Formula: C13H28O4
• Molecular Weight: 248.363
• UNII: K0N34Z34O8
• DSSTox Substance ID: DTXSID90973032
• Nikkaji Number: J1.781.507E
• Wikidata: Q27896607
• Mol file: 57499-93-1.mol

Synonyms:57499-93-1;Tripropylene glycol mono-n-butyl ether;ppg-3 butyl ether;Dowanol 66B;1-((1-((1-Butoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol;BRN 1704643;1-[1-(1-butoxypropan-2-yloxy)propan-2-yloxy]propan-2-ol;1-({1-[(1-BUTOXYPROPAN-2-YL)OXY]PROPAN-2-YL}OXY)PROPAN-2-OL;1-(2-(2-Butoxy-1-methylethoxy)-1-methylethoxy)-2-propanol;2-Propanol, 1-(2-(2-butoxy-1-methylethoxy)-1-methylethoxy)-;2-Propanol, 1-[2-(2-butoxy-1-methylethoxy)-1-methylethoxy]-;SCHEMBL15374;DTXSID90973032;LORVPHHKJFSORQ-UHFFFAOYSA-N;K0N34Z34O8;PPG-3 BUTYL ETHER [INCI];AS-63503;LS-121809;Propanol, [(butoxymethylethoxy)methylethoxy]-;5,8-Dimethyl-4,7,10-trioxatetradecane-2-ol;D93141;A905620;Q27896607

Chemical Property of Tripropylene glycol mono-n-butyl ether

Chemical Property:

• Boiling Point: 322.4°Cat760mmHg
• Flash Point: 148.8°C
• PSA: 47.92000
• Density: 0.952g/cm³
• LogP: 1.99410
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 11
• Exact Mass: 248.19875937
• Heavy Atom Count: 17
• Complexity: 164

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCOCC(C)OCC(C)OCC(C)O

Technology Process of Tripropylene glycol mono-n-butyl ether

There total 3 articles about Tripropylene glycol mono-n-butyl 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:

methyloxirane (75-56-9,16033-71-9) + butan-1-ol (71-36-3) → 1-((1-((1-butoxy-2-propanyl)oxy)-2-propanyl)oxy)-2-propanol (57499-93-1)

Guidance literature:

With sodium hydroxide; at 190 ℃; under 11032.6 Torr;

Reference yield:

sodium butanolate (2372-45-4) + methyloxirane (75-56-9,16033-71-9) → 1-((1-((1-butoxy-2-propanyl)oxy)-2-propanyl)oxy)-2-propanol (57499-93-1)

Guidance literature:

In butan-1-ol;

Reference yield:

→ 1-((1-((1-butoxy-2-propanyl)oxy)-2-propanyl)oxy)-2-propanol (57499-93-1)

Guidance literature:

Entspr. Propylenoxid, n-Butanol;

DOI:10.1016/0032-3950(69)90195-6

upstream raw materials:

methyloxirane

butan-1-ol

sodium butanolate

Downstream raw materials:

Phosphoric acid monododecyl ester