O3303
1,8-Octanediol
98%
Sinonimo/i:
Octamethylene glycol
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About This Item
Prodotti consigliati
Livello qualitativo
Saggio
98%
P. ebollizione
172 °C/20 mmHg (lit.)
Punto di fusione
57-61 °C (lit.)
Stringa SMILE
OCCCCCCCCO
InChI
1S/C8H18O2/c9-7-5-3-1-2-4-6-8-10/h9-10H,1-8H2
OEIJHBUUFURJLI-UHFFFAOYSA-N
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Categorie correlate
Applicazioni
1,8-Octanediol can undergo:
- Polycondensation with citric acid to form biodegradable poly(1,8-octanediol citrate)(POC) crosslinked bioelastomer which can be blended with various additives.
- Fischer esterification with dicarboxylic acids to form diol-based macromers.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
248.0 °F - closed cup
Punto d’infiammabilità (°C)
120 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Biomacromolecules, 18(6), 1724-1735 (2017-05-11)
In this work, we describe the synthesis and characterization of variants of poly(diol fumarate) and poly(diol fumarate-co-succinate). Through a Fischer esterification, α,ω-diols and dicarboxylic acids were polymerized to form aliphatic polyester comacromers. Because of the carbon-carbon double bond of fumaric
International journal of biological macromolecules, 116, 217-223 (2018-05-04)
Long carbon chain alkanediols are used in the production of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)], however these substrates possess high toxicity towards bacterial cells. This study demonstrated the effective utilisation of a long carbon chain alkanediol, namely 1,8-octanediol, to enhance the yield and
Development of poly (1, 8-octanediol citrate)/chitosan blend films for tissue engineering applications.
Carbohydrate Polymers, 175, 618-627 (2017)
PloS one, 12(8), e0182971-e0182971 (2017-08-12)
To explore the repairing effect of combination of adipose stem cells (ASCs) and composite scaffolds on CWR, the electrospun Poly 1, 8-octanediol-co-citric acid (POC)-poly-L-lactide acid (PLA) composite scaffolds were prepared, followed by in vitro and in vivo biocompatibility evaluation of
Acta biomaterialia, 93, 180-191 (2019-03-31)
The design and development of bioactive materials that are inherently conducive for osteointegration and bone regeneration with tunable mechanical properties and degradation remains a challenge. Herein, we report the development of a new class of citrate-based materials with glycerophosphate salts
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