| Identification | Back Directory | [Name]
1,5-Pentanediol diacrylate | [CAS]
36840-85-4 | [Synonyms]
Ccris 7043
Einecs 253-235-8
Pentamethylene Diacrylate
1,5-pentanediyl diacrylate
1,5-PENTANEDIOL DIACRYLATE
Pentane-1,5-diyl diacrylate
1,5-Bis(acryloyloxy)pentane
1,5-Pentamethylene Diacrylate
Bispropenoic acid 1,5-pentanediyl
1,5-PENTAMETHYLENE GLYCOL DIACRYLATE
5-prop-2-enoyloxypentyl prop-2-enoate
Bisacrylic acid pentane-1,5-diyl ester
1,5-Pentanediol diacrylate homopolymer
2-Propenoic acid, 1,5-pentanediyl ester
2-Propenoic acid, 1,1'-(1,5-pentanediyl) ester
1,5-Pentanediol diacrylate (stabilized with MEHQ)
1,5-Bis(acryloyloxy)pentane (stabilized with MEHQ)
1,5-Pentanediol Diacrylate
Pentamethylene Glycol Diacrylate
N′,N′-(4,10-dioxa-3,11-dioxo-tridecanylene)-1,13-bis(1,2,3,4-tetrahydroisoquinoline)-bioxalate AND 1,5-Pentamethylene Diacrylate | [EINECS(EC#)]
253-235-8 | [Molecular Formula]
C11H16O4 | [MDL Number]
MFCD00078444 | [MOL File]
36840-85-4.mol | [Molecular Weight]
212.24 |
| Chemical Properties | Back Directory | [Boiling point ]
90-95 °C(Press: 0.1 Torr) | [density ]
1.024±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Soluble) | [form ]
liquid | [color ]
Yellow | [InChI]
InChI=1S/C11H16O4/c1-3-10(12)14-8-6-5-7-9-15-11(13)4-2/h3-4H,1-2,5-9H2 | [InChIKey]
XAMCLRBWHRRBCN-UHFFFAOYSA-N | [SMILES]
C(OC(=O)C=C)CCCCOC(=O)C=C |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to pale yellow liquid | [Uses]
1,5-Pentanediol Diacrylate (Stabilized with Hydroquinone) is used in reparation method of PUV cured polythiol resin and cured film. | [Synthesis]
a) 1,5-Pentanediol (15.6 g) was heated at reflux with 3-bromopropionic acid (50.5 g) and trace amounts of p-toluenesulfonic acid in toluene (500 mL) for 4 hours. After completion of the reaction, the toluene solution was cooled and washed with aqueous sodium acetate. Subsequently, triethylamine (50 mL) was added under reflux conditions. After cooling the reaction mixture, it was washed well with water to remove triethylamine and triethylamine hydrobromide. Toluene was removed by distillation under reduced pressure and finally purified by high-vacuum distillation (boiling point 90°C-95°C/0.1 mmHg) to afford 1,5-pentanediol diacrylate (24.0 g, 75% yield) as a light-colored liquid. | [References]
[1] Patent: US5453510, 1995, A |
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