5-Hydroxypentyl acrylate

Base Information

• Chemical Name: 5-Hydroxypentyl acrylate
• CAS No.: 57198-94-4
• Molecular Formula: C8H14 O3
• Molecular Weight: 158.197
• European Community (EC) Number: 260-613-6
• UNII: 7SPP26XW3H
• DSSTox Substance ID: DTXSID30205829
• Nikkaji Number: J349.106D
• Wikidata: Q83079518
• Mol file: 57198-94-4.mol

Synonyms:5-Hydroxypentyl acrylate;57198-94-4;5-hydroxypentyl prop-2-enoate;7SPP26XW3H;EINECS 260-613-6;5-hydroxypentylacrylate;UNII-7SPP26XW3H;1,5-pentanediol monoacrylate;SCHEMBL396968;DTXSID30205829;Propenoic acid 5-hydroxypentyl ester;5-HYDROXYPENTYL 2-PROPENOATE;BS-48506;F72355

Chemical Property of 5-Hydroxypentyl acrylate

Chemical Property:

• Vapor Pressure: 0.00824mmHg at 25°C
• Boiling Point: 237°Cat760mmHg
• PKA: 15.11±0.10(Predicted)
• Flash Point: 93.8°C
• PSA: 46.53000
• Density: 1.009g/cm³
• LogP: 0.87820
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 158.094294304
• Heavy Atom Count: 11
• Complexity: 121

Purity/Quality:

98%Min ^*data from raw suppliers

5-HydroxypentylAcrylate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC(=O)OCCCCCO

Technology Process of 5-Hydroxypentyl acrylate

There total 4 articles about 5-Hydroxypentyl acrylate 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:

1 ,5-pentanediol (111-29-5) + acryloyl chloride (814-68-6,25189-84-8) → hydroxypentyl acrylate (57198-94-4)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 5h;

Reference yield:

1 ,5-pentanediol (111-29-5) + acrylic acid methyl ester (292638-85-8,9003-21-8,96-33-3) → pentamethylene 1,5-diacrylate (36840-85-4) + hydroxypentyl acrylate (57198-94-4)

Guidance literature:

With Novozyme 435; In tert-Amyl alcohol; at 50 ℃; for 120h; Inert atmosphere; Molecular sieve; Enzymatic reaction;

DOI:10.1016/j.molcatb.2009.09.008

Reference yield:

1 ,5-pentanediol (111-29-5) + acrylic acid (79-10-7) → hydroxypentyl acrylate (57198-94-4)

Guidance literature:

toluene-4-sulfonic acid;

upstream raw materials:

1 ,5-pentanediol

acrylic acid

acrylic acid methyl ester

acryloyl chloride

Refernces

• 1、 Popescu, Dragos,Hoogenboom, Richard,Keul, Helmut,Moeller, Martin. "Hydroxy functional acrylate and methacrylate monomers prepared via lipase-catalyzed transacylation reactions". experimental part. p. 80 - 89. Retrieved 2010/08/20.
• 2、 Kumakura, M.,Kojima, T.,Kaetsu, I.. "FIBROUS POLYMERIC COMPOSITES IMMOBILIZING GLUCOSE OXIDASE". . p. 65 - 72. Retrieved 2007/10/02.