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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
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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
[The study of immunotoxicity of butyl glycidyl ether].
B Xue et al.
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine], 22(1), 11-13 (1988-01-01)
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
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