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84840

Sigma-Aldrich

Dibutyl sebacate

≥97.0% (GC)

Synonym(s):

Decanedioic acid dibutyl ester, Sebacic acid dibutyl ester

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250 ML
$79.38
1 L
$118.00

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250 ML
$79.38
1 L
$118.00

About This Item

Linear Formula:
[-(CH2)4CO2(CH2)3CH3]2
CAS Number:
Molecular Weight:
314.46
Beilstein/REAXYS Number:
1798308
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

$79.38

List Price$88.20Save 10%

In StockDetails


Request a Bulk Order

Quality Level

assay

≥97.0% (GC)

form

liquid

refractive index

n20/D 1.441 (lit.)
n20/D 1.441

bp

178-179 °C/3 mmHg (lit.)

density

0.936 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CCCCOC(=O)CCCCCCCCC(=O)OCCCC

InChI

1S/C18H34O4/c1-3-5-15-21-17(19)13-11-9-7-8-10-12-14-18(20)22-16-6-4-2/h3-16H2,1-2H3

InChI key

PYGXAGIECVVIOZ-UHFFFAOYSA-N

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Application

Dibutyl sebacate has been used as a plasticizer to prepare free ethylcellulose films.[1][2] It can be utilized as a core in liquid-core capsules with cross-linked alginate/polyacrylamide membrane prepared via co-extrusion jet-break-up method for the extraction of the pesticide, atrazine.[2]

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

366.8 °F - open cup

flash_point_c

186 °C - open cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Micro-encapsulated organic phase for enhanced bioremediation of hydrophobic organic pollutants.
Wyss A, et al.
Enzyme and Microbial Technology, 40(1), 25-31 (2006)
Physico-mechanical analysis of free ethylcellulose films plasticized with incremental weight percents of dibutyl sebacate.
Kangarlou S and Haririan I
Iranian Journal of Pharmaceutical Sciences, 3(3), 135-142 (2007)
Kangarlou Sogol et al.
International journal of pharmaceutics, 408(1-2), 1-8 (2010-11-26)
The object of this study was to investigate the influence of static and dynamic forces on mechanical properties of the biocompatible polymer ethyl cellulose. Similar polymeric films containing 40% (w/w) of the plasticizer dibutyl sebacate were subjected to tensile forces
T Quinten et al.
Drug development and industrial pharmacy, 37(2), 149-159 (2010-07-10)
It was the aim of the present study to develop sustained-release matrix tablets by means of injection molding of ethylcellulose (EC) and polyethylene oxide (PEO) mixtures and to evaluate the influence of process temperature, matrix composition, and viscosity grade of
I J Hardy et al.
International journal of pharmaceutics, 311(1-2), 26-32 (2006-01-25)
The compression and compaction properties of plasticised high molecular weight USP2208 HPMC were investigated with the aim of improving tablet formation in HPMC matrices. Experiments were conducted on binary polymer-plasticiser mixtures containing 17 wt.% plasticiser, and on a model hydrophilic

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