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537535

Sigma-Aldrich

2-(2-Butoxyethoxy)ethyl acetate

≥99.2%

Synonym(s):

Butyldiglycol acetate, Diethylene glycol monobutyl ether acetate

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About This Item

Linear Formula:
CH3COOCH2CH2OCH2CH2O(CH2)3CH3
CAS Number:
Molecular Weight:
204.26
Beilstein:
1771533
EC Number:
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.21

Quality Level

Assay

≥99.2%

form

liquid

autoignition temp.

393 °F

expl. lim.

0.76 %, 135 °F
10.7 %, 203 °F

impurities

≤0.10% (water)

refractive index

n20/D 1.423 (lit.)

bp

245 °C (lit.)

mp

-32 °C

solubility

water: soluble 65 g/L at 20 °C

density

0.978 g/mL at 25 °C (lit.)

SMILES string

CCCCOCCOCCOC(C)=O

InChI

1S/C10H20O4/c1-3-4-5-12-6-7-13-8-9-14-10(2)11/h3-9H2,1-2H3

InChI key

VXQBJTKSVGFQOL-UHFFFAOYSA-N

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General description

2-(2-Butoxyethoxy)ethyl acetate (Butyldiglycol acetate, BGDA) is a volatile organic compound that can be prepared by reacting diethylene glycol monobutyl ether with acetic acid using strongly acidic cationic exchange resin as catalyst.

Application

2-(2-Butoxyethoxy)ethyl acetate (Butyldiglycol acetate) may be used as a component to reduce the minimal film forming temperature (MTF) during poly(vinyl acetate)(PVAc) based composite film preparation. It may also be used during the formulation of thick film pastes of silver.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

215.6 °F - closed cup

Flash Point(C)

102 °C - closed cup


Certificates of Analysis (COA)

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Influence of surfactants treatment on silver powder and its thick films.
Rane SB, et al.
Materials Letters, 57(20), 3096-3100 (2003)
Organic compounds in indoor air-their relevance for perceived indoor air quality?
Wolkoff P and Nielsen GD.
Atmospheric Environment, 35(26), 4407-4417 (2001)
Composites of poly(vinyl acetate) filled with calcium carbonate: microscopy, diffractometry and thermophysical properties.
Kovacevic V, et al.
Polym. Eng. Sci., 39(8), 1433-1443 (1999)
P J Deisinger et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(9), 981-989 (1989-09-01)
1. The in vitro hydrolysis of DGBA in rat blood and its in vivo metabolism and disposition in male Sprague-Dawley rats were studied. 2. DGBA (5 mM) was hydrolysed in rat blood to diethylene glycol monobutyl ether (DGBE) with a
Delayed and immediate hypersensitivity to carbitols.
T A Dawson et al.
Contact dermatitis, 21(1), 52-53 (1989-07-01)

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