추천 제품
Quality Level
분석
≥99.2%
양식
liquid
autoignition temp.
393 °F
expl. lim.
0.76 %, 135 °F
10.7 %, 203 °F
불순물
≤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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
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.
애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
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
이미 열람한 고객
Influence of surfactants treatment on silver powder and its thick films.
Materials Letters, 57(20), 3096-3100 (2003)
Organic compounds in indoor air-their relevance for perceived indoor air quality?
Atmospheric Environment, 35(26), 4407-4417 (2001)
Composites of poly(vinyl acetate) filled with calcium carbonate: microscopy, diffractometry and thermophysical properties.
Polym. Eng. Sci., 39(8), 1433-1443 (1999)
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
Toxicology letters, 156(1), 117-126 (2005-02-12)
2-Methoxyacetic and 2-ethoxyacetic acids are well known toxic metabolites of 2-alkoxyethanols. The use of 2-alkoxyethanols is now restricted, and the regulations have forced manufacturers to find substitutive solvents, 2-(2-alkoxyethoxy)ethanols. 2-(2-Alkoxyethoxy)ethanols resemble 2-alkoxyethanols, and their most hazardous similarity is their ability
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