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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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
A Bertuzzi et al.
Biochemical pharmacology, 45(3), 697-702 (1993-02-09)
Sebacic (decanedioic) acid is a dicarboxylic acid proposed recently as an alternative energy substrate in total parenteral nutrition. In this paper, binding of sebacic acid to defatted human plasma albumin, also in the presence of decanoic acid, was studied by
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
A Curcoy et al.
Molecular genetics and metabolism, 78(4), 247-249 (2003-04-23)
Multiple acyl-CoA-dehydrogenase deficiency (MADD) or glutaric aciduria type II (GAII) are a group of metabolic disorders due to deficiency of either electron transfer flavoprotein (ETF) or electron transfer flavoprotein ubiquinone oxidoreductase (ETF-QO). We report the clinical features and biochemical and
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