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84809
Sebacinsäure
≥95.0% (GC)
Synonym(e):
Decandisäure
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CHF 39.30
1 KG
CHF 90.60
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100 G
CHF 39.30
1 KG
CHF 90.60
About This Item
Lineare Formel:
HO2C(CH2)8CO2H
CAS-Nummer:
Molekulargewicht:
202.25
Beilstein:
1210591
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Dampfdruck
1 mmHg ( 183 °C)
Assay
≥95.0% (GC)
bp
294.5 °C/100 mmHg (lit.)
mp (Schmelzpunkt)
133-137 °C (lit.)
Funktionelle Gruppe
carboxylic acid
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)
InChIKey
CXMXRPHRNRROMY-UHFFFAOYSA-N
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Verwandte Kategorien
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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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
Easy fabrication and morphology control of supramolecular liquid-crystalline polymer microparticles.
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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