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325481

Sigma-Aldrich

Furfuryl glycidyl ether

96%

Synonym(s):

2-((2,3-Epoxypropoxy)methyl)furan, furfurylglycidyl ether, 2,3-Epoxypropyl 2-furylmethyl ether, 2-[(Oxiranylmethoxy)methyl]furan

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About This Item

Empirical Formula (Hill Notation):
C8H10O3
CAS Number:
5380-87-0
Molecular Weight:
154.16
EC Number:
226-372-6
MDL number:
MFCD00013348
UNSPSC Code:
12162002
PubChem Substance ID:
24859513
NACRES:
NA.23

Assay

96%

form

liquid

refractive index

n20/D 1.481 (lit.)

bp

103-104 °C/11 mmHg (lit.)

density

1.122 g/mL at 25 °C

SMILES string

C(OCc1ccco1)C2CO2

InChI

1S/C8H10O3/c1-2-7(10-3-1)4-9-5-8-6-11-8/h1-3,8H,4-6H2

InChI key

RUGWIVARLJMKDM-UHFFFAOYSA-N

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Application

  • The synthesis of multifunctional cellulose graft alternating copolymers of 3,4-dihydrocoumarin and epoxides in DBU/DMSO/CO(2) solvent system.: This study outlines the development of cellulose-based graft copolymers for potential use in advanced material applications, highlighting the incorporation of furfuryl glycidyl ether for improved performance (Guo et al., 2023).
  • High-Performance Reversible Furan-Maleimide Resins Based on Furfuryl Glycidyl Ether and Bismaleimides.: Research on novel resin systems employing furfuryl glycidyl ether to enhance reversibility and performance in composite materials, with applications in aerospace and automotive industries (Wang et al., 2023).
  • Multi-Armed Star-Shaped Block Copolymers of Poly(ethylene glycol)-Poly(furfuryl glycidol) as Long Circulating Nanocarriers.: This publication discusses the use of furfuryl glycidyl ether in the creation of block copolymers for drug delivery systems, emphasizing the enhancement of circulation times and biocompatibility (Nakagawa et al., 2023).
  • Structure and Properties of Epoxy Polysulfone Systems Modified with an Active Diluent.: Investigation into the effects of furfuryl glycidyl ether as a modifier in epoxy systems, aiming to improve the mechanical properties and heat resistance of the resulting polymers, suitable for industrial applications (Petrova et al., 2022).
  • Star-Shaped Poly(furfuryl glycidyl ether)-Block-Poly(glyceryl glycerol ether) as an Efficient Agent for the Enhancement of Nifuratel Solubility and for the Formation of Injectable and Self-Healable Hydrogel Platforms for the Gynaecological Therapies.: Details a unique use of furfuryl glycidyl ether in medical hydrogel platforms, offering potential advancements in gynecological treatments and drug delivery systems (Ziemczonek et al., 2021).

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

215.6 °F - closed cup

Flash Point(C)

102.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC2112V
BGBB9405
BGBB6737
1438300
MKAA2457

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Shweta AnilKumar et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 107(2), 314-323 (2018-04-16)
Three-dimensional bioprinting is an innovative technique in tissue engineering, to create layer-by-layer structures, required for mimicking body tissues. However, synthetic bioinks do not generally possess high printability and biocompatibility at the same time. So, there is an urgent need for
Bo Bi et al.
Carbohydrate polymers, 212, 368-377 (2019-03-06)
Injectable thermosensitive hydrogels crosslinked physically have been extensively studied as scaffolds in biomedical field, however, their low gel stability with weak strength limits their potential applications. Here, a novel thermosensitive furyl-modified hydroxypropyl chitin polymer was synthesized homogeneously in aqueous solution
Yi-Huan Lee et al.
Polymers, 11(11) (2019-11-17)
In this study, a novel biobased poly(ethylene brassylate)-poly(furfuryl glycidyl ether) copolymer (PEBF) copolymer was synthesized and applied as a structure-directing template to incorporate graphene and 1,1'-(methylenedi-4,1-phenylene)bismaleimide (BMI) to fabricate a series of self-healing organic/inorganic hybrid materials. This ternary material system
Beata Strachota et al.
Polymers, 11(6) (2019-05-31)
Reversible Diels-Alder (DA) type networks were prepared from furan and maleimide monomers of different structure and functionality. The factors controlling the dynamic network formation and their properties were discussed. Evolution of structure during both dynamic nonequilibrium and isothermal equilibrium network

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