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377031

Sigma-Aldrich

Butyl glycidyl ether

95%

Synonym(s):

(Butoxymethyl)oxirane, Araldite® RD-1

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About This Item

Empirical Formula (Hill Notation):
C7H14O2
CAS Number:
2426-08-6
Molecular Weight:
130.18
Beilstein:
103668
EC Number:
219-376-4
MDL number:
MFCD00005145
UNSPSC Code:
12162002
PubChem Substance ID:
24863488
NACRES:
NA.23

Assay

95%

form

liquid

refractive index

n20/D 1.418 (lit.)

bp

164-166 °C (lit.)

density

0.91 g/mL at 25 °C (lit.)

SMILES string

CCCCOCC1CO1

InChI

1S/C7H14O2/c1-2-3-4-8-5-7-6-9-7/h7H,2-6H2,1H3

InChI key

YSUQLAYJZDEMOT-UHFFFAOYSA-N

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General description

Butyl glycidyl ether is an epoxy monomer that is mainly used as an aliphatic reactive diluent in the modification of epoxy systems. Its structure consists of a soft segment and one epoxy segment which can be incorporated into the epoxy resins for reducing the viscosity. It facilitates and enhances the mechanical properties by improving the cryogenic strength, ductility and impact resistance of the polymers.

Legal Information

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Muta. 2 - Repr. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

129.2 °F - closed cup

Flash Point(C)

54 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Mechanical property characterization of a polymeric nanocomposite reinforced by graphitic nanofibers with reactive linkers
Xu LR, et al.
Journal of Composite Materials, 38(18), 1563-1582 (2004)
Simultaneously increasing cryogenic strength, ductility and impact resistance of epoxy resins modified by n-butyl glycidyl ether
Chen Z, et al.
Polymer, 50(5), 1316-1323 (2009)
Preparation and characterization of layered silicate/glass fiber/epoxy hybrid nanocomposites via vacuum-assisted resin transfer molding (VARTM)
Lin L, et al.
Composites Science and Technology, 66(13), 2116-2125 (2006)
Paul F Gratzer et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 81(1), 1-11 (2006-08-23)
In this study, the effects of specific chemical modifications of amino acid side-chains on the in vitro enzyme degradation of type I collagen was studied. Two monofunctional epoxides of different size and chemistry were used to modify lysine and methylglyoxal
n-Butylglycidyl ether: the formation of a novel metabolite of an epoxide.
C V Eadsforth et al.
Drug metabolism and disposition: the biological fate of chemicals, 13(2), 263-264 (1985-03-01)
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