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84809

Sigma-Aldrich

Sebacic acid

≥95.0% (GC)

Synonym(s):

Decanedioic acid

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About This Item

Linear Formula:
HO2C(CH2)8CO2H
CAS Number:
111-20-6
Molecular Weight:
202.25
Beilstein:
1210591
EC Number:
203-845-5
MDL number:
MFCD00004440
UNSPSC Code:
12352100
PubChem Substance ID:
57653024
NACRES:
NA.22

vapor pressure

1 mmHg ( 183 °C)

Assay

≥95.0% (GC)

bp

294.5 °C/100 mmHg (lit.)

mp

133-137 °C (lit.)

SMILES string

OC(=O)CCCCCCCCC(O)=O

InChI

1S/C10H18O4/c11-9(12)7-5-3-1-2-4-6-8-10(13)14/h1-8H2,(H,11,12)(H,13,14)

InChI key

CXMXRPHRNRROMY-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Magdalena Kwiatkowska et al.
Polymers, 12(2) (2020-02-08)
In this work the preparation of polyamide 12 (PA12) based composites reinforced with pristine and surface-modified carbon nanotubes is reported. A qualitative and quantitative evaluation of multi-walled carbon nanotube functionalization with oxygen containing reactive groups achieved by different procedures of
Hyung-seok Park et al.
Acta biomaterialia, 8(8), 2911-2918 (2012-04-24)
High molecular weight biodegradable polyesters were prepared from sebacic acid, ethylene glycol and butylene glycol through a simple non-solvent polycondensation with a low toxicity catalyst. The successful synthesis of the polyesters was confirmed by gel permeation chromatography, (1)H-nuclear magnetic resonance
Senja K Lopac et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 91(2), 938-947 (2009-07-31)
The release kinetics and stability of ovalbumin encapsulated into polyanhydride microspheres with varying chemistries were studied. Polymers based on the anhydride monomers sebacic acid (SA), 1,6-bis(p-carboxyphenoxy)hexane (CPH), and 1,8-bis (p-carboxyphenoxy)-3,6-dioxaoctane (CPTEG) were utilized. Microspheres were fabricated using two non-aqueous methods:
Christiane L Salgado et al.
Tissue engineering. Part A, 18(1-2), 137-146 (2011-09-10)
Tissue engineering constitutes a promising alternative technology to transplantation medicine by creating viable substitutes for failing tissues or organs. The ability to manipulate and reconstitute tissue function has tremendous clinical implications and will most likely play a key role in
Hui Liu et al.
Macromolecular rapid communications, 32(4), 378-383 (2011-03-25)
A novel kind of supramolecular liquid-crystalline polymer (SLCP) microparticles was successfully fabricated with an azopyridyl polymer and sebacic acid by combining a simple self-organized precipitation method with hydrogen bonding interactions. Upon slow evaporation of a mixed solution of a volatile
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