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Merck

84840

Dibutyl sebacate

≥97.0% (GC)

Synonym(s):

Decanedioic acid dibutyl ester, Sebacic acid dibutyl ester

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About This Item

Linear Formula:
[-(CH2)4CO2(CH2)3CH3]2
CAS Number:
109-43-3
Molecular Weight:
314.46
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57653026
EC Number:
203-672-5
Beilstein/REAXYS Number:
1798308
MDL number:
MFCD00027218

Key Documents

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Product Name

Dibutyl sebacate, ≥97.0% (GC)

InChI key

PYGXAGIECVVIOZ-UHFFFAOYSA-N

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

SMILES string

CCCCOC(=O)CCCCCCCCC(=O)OCCCC

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

Quality Level

100

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Application

Dibutyl sebacate has been used as a plasticizer to prepare free ethylcellulose films. 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.

Storage Class

10 - Combustible liquids

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9149
BCCM5294
BCCJ1718
BCCJ3412
BCCG5403

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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)
T Quinten et al.
Journal of pharmaceutical sciences, 100(7), 2858-2870 (2011-01-22)
Sustained-release matrix tablets were developed by injection moulding using metoprolol tartrate (MPT) and ethylcellulose (EC) as sustained-release agent. Dibutyl sebacate was selected as plasticiser. The influence of matrix composition, plasticiser concentration, and drug load on drug release was evaluated. The
Maarit Tarvainen et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 19(5), 363-371 (2003-08-09)
The aim of this study was to investigate the ability of n-alkenyl succinic anhydrides (n-ASAs) to improve the film-forming characteristics of a novel coating polymer, potato starch acetate degree of substitution 2.8 (SA). n-ASAs were also applied to improve the
D Stark et al.
Biotechnology and bioengineering, 83(4), 376-385 (2003-06-12)
A novel in situ product removal (ISPR) method that uses microcapsules to extract inhibitory products from the reaction suspension is introduced into fermentation technology. More specifically, L-phenylalanine (L-Phe) was transformed by Saccharomyces cerevisiae to 2-phenylethanol (PEA), which is inhibitory toward
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