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Merck
CN

291455

Butyl glycidyl ether

97%

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
PubChem Substance ID:
329753315

Key Documents

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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

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Legal Information

Araldite is a registered trademark of Huntsman Advanced Materials Inc.

Signal Word

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 Code

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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Certificates of Analysis (COA)

Lot/Batch Number
03618JM

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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
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
C V Eadsforth et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(7), 579-589 (1985-07-01)
[1-14C]Butyl glycidyl ether administered orally to male rats and rabbits (20 mg/kg) is rapidly absorbed and metabolized. Most of the administered compound, 87% (rat) and 78% (rabbit), is eliminated in the 0-24 urine. Major metabolites in the rat include 3-butoxy-2-hydroxypropionic
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