Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

291455

Butyl glycidyl ether

97%

Synonym(s):

(Butoxymethyl)oxirane, Araldite® RD-1

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C7H14O2
CAS Number:
2426-08-6
Molecular Weight:
130.18
Beilstein/REAXYS Number:
103668
EC Number:
219-376-4
MDL number:
MFCD00005145
PubChem Substance ID:
329753315
Pricing and availability is not currently available.

assay

97%

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

Looking for similar products? Visit Product Comparison Guide

Legal Information

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
03618JM

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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)
T H Connor et al.
Environmental mutagenesis, 2(4), 521-530 (1980-01-01)
The epoxide diluent, n-butylglycidyl ether (n-BGE), was tested in vitro for mutagenicity using Salmonella typhimurium and for transforming ability in mouse embryo cells (BAlb/3T3-A31-1-13). The n-BGE produced base-pair type mutations in S typhimurium strains TA1535 and TA100. However, it failed
Mohammad F Bostanudin et al.
Polymers, 11(5) (2019-05-06)
Pectin is a polysaccharide with very good gel forming properties that traditionally has found important applications in foods and pharmaceutical industries. Although less studied, chemical modifications of pectin leading to a decrease in its hydrophilicity can be useful for the
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service