Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether

1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether

Basic information Uses Safety Supplier Related

1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether Basic information

Product Name:
1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether
Synonyms:
  • 1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether
  • PENTAERYTHRITOL TRIALLYL ETHER, TECH., 7 0%
  • Allyl pentaerythritol
  • pentaerythritol allyl ether
  • 2,2-Bis(hydroxymethyl)-1,3-propanediol allyl ether
  • 2,2-Bis-(hydroxymethyl)-1,3-propanediol allyl ester
  • 2-(4-(allyloxy)hepta-1,6-dien-4-yl)-2-(hydroxyMethyl)hex-5-ene-1,3-diol
  • Pentaerythritol allyl ether technical grade, 70%
CAS:
91648-24-7
MF:
C14H24O4
MW:
256.33796
EINECS:
293-883-9
Product Categories:
  • Allyl Monomers
  • Monomers
  • Polymer Science
Mol File:
91648-24-7.mol
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1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether Chemical Properties

Boiling point:
100 °C/0.1 mmHg(lit.)
Density 
0.985 g/mL at 25 °C(lit.)
vapor pressure 
0.113Pa at 25℃
refractive index 
n20/D 1.465(lit.)
Flash point:
113 °C
form 
liquid
Water Solubility 
3.49g/L at 20℃
InChI
InChI=1S/C8H16O4/c1-2-3-12-7-8(4-9,5-10)6-11/h2,9-11H,1,3-7H2
InChIKey
RFIMISVNSAUMBU-UHFFFAOYSA-N
SMILES
C(CO)(CO)(CO)COCC=C
LogP
2.93 at 25℃
EPA Substance Registry System
1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether (91648-24-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-52/53
Safety Statements 
26-27-28-36-61
WGK Germany 
2
RTECS 
TY3339500
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1,3-Propanediol, 2,2-bis(hydroxymethyl)-, allyl ether Usage And Synthesis

Uses

Due to the presence of active groups such as ether groups, olefin bonds, and hydroxyl groups, pentaerythritol allyl ethers are often used as chain extenders in the synthesis of polymers such as superabsorbent resins, thickeners, unsaturated polyesters, polyurethane resins, epoxy resins, and UV-curable resins, while also imparting self-drying properties to the polymers. Industrially, mixtures of pentaerythritol allyl ethers, primarily composed of pentaerythritol triallyl ether, are commonly used, with the most common mixtures having a pentaerythritol triallyl ether content between 70% and 90% by mass.

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