Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C7H14O2
CAS Number:
Molecular Weight:
130.18
EC Number:
219-376-4
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
103668
InChI
1S/C7H14O2/c1-2-3-4-8-5-7-6-9-7/h7H,2-6H2,1H3
InChI key
YSUQLAYJZDEMOT-UHFFFAOYSA-N
SMILES string
CCCCOCC1CO1
assay
97%
refractive index
n20/D 1.418 (lit.)
bp
164-166 °C (lit.)
density
0.91 g/mL at 25 °C (lit.)
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
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:
Already Own This Product?
Find documentation for the products that you have recently purchased in 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
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
L-J Chen et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(12), 2218-2224 (2007-09-19)
The disposition of [(14)C]-labeled n-butyl glycidyl ether (BGE, 3-butoxy-1,2-epoxypropane) was studied in rats and mice. The majority of a single p.o. dose (2-200 mg/kg) was excreted in urine (rats, 84-92%; mice, 64-73%) within 24 h. The rest of the dose
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