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Merck

377031

Sigma-Aldrich

Butyl glycidyl ether

95%

Sinónimos:

(Butoxymethyl)oxirane, Araldite® RD-1

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About This Item

Fórmula empírica (notación de Hill):
C7H14O2
Número de CAS:
Peso molecular:
130.18
Beilstein/REAXYS Number:
103668
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Quality Level

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.

signalword

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

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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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)
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)
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)
E B Whorton et al.
Mutation research, 124(3-4), 225-233 (1983-12-01)
Using the dominant lethal assay, the ability of n-butyl glycidyl ether to induce mutations in male mice was investigated. No significant dose-related changes either in pregnancy rates or in average number of implants per pregnant female were found. However, while

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