Science Elevated.

sales@fluoromart.com

0Your Cart$0.00

Cart (0)

No products in the cart.

80806-68-4 | 4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononan-1-ol

$396.00$396.00

Weight:

Purity:

Purchase CAS:80806-68-4,view related peer-reviewed papers,technical documents,similar products,MSDS & more.
4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononan-1-ol, also known as FDN or FDN-1, is a fluorinated alcohol that has been studied extensively in recent years due to its unique properties. FDN-1 has a wide range of applications, from being used as a surfactant in cosmetics to being used as a solvent in the synthesis of phar...

sds

SKU:FM621243
Categories: Surface Materials
HazMat Fast
HazMat Fast
Global Delivery About 12 days
Research Only
Research Only
All products for research only
Compliant Shipping
Compliant Shipping
Comply global express rules
Split Packaging
Split Packaging
Split packaging options free
Easy Relabeling
Easy Relabeling
With easy-to-change labels
Easy Labels

CAS:80806-68-4 | 4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononan-1-ol ,Description

4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononan-1-ol, also known as FDN or FDN-1, is a fluorinated alcohol that has been studied extensively in recent years due to its unique properties. FDN-1 has a wide range of applications, from being used as a surfactant in cosmetics to being used as a solvent in the synthesis of pharmaceuticals. FDN-1 is also of interest due to its potential as a bioactive compound, with potential applications in biomedicine and biotechnology. 
 

Scientific Research Applications

 

Hemocompatibility and Co-emulsifying Properties

A study by Paleta et al. (2002) synthesized a novel compound, 1-O-(4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononyl)xylitol, to assess its hemocompatibility and co-emulsifying properties in microemulsions for biomedical uses. This research found the compound to exhibit very good hemocompatibility and co-emulsifying properties, indicating potential applications in medical formulations and drug delivery systems Paleta et al., 2002.

Energetic Material Synthesis

Garg and Shreeve (2011) explored the synthesis of 4-(Trifluoromethyl- or pentafluorosulfanyl)-substituted mono- and poly-1,2,3-triazole compounds. They used a methodology involving Cu(I)-catalyzed 1,3-dipolar azide and fluorinated alkyne cycloaddition reactions, leading to regioselective products with high thermal stability and detonation properties. This research suggests the potential of incorporating such fluoroalkylated compounds in the design of stable energetic materials Garg & Shreeve, 2011.

Advanced Nuclear Fuel Cycle Research

In the field of nuclear fuel cycles, research by Neidig, Clark, and Martin (2013) on covalency in f-element complexes highlighted the relevance of understanding bonding in f-element complexes for separating trivalent trans-plutonium elements from lanthanide fission products. Their review discusses the key evidence for covalency derived from structural, spectroscopic, and theoretical studies, which is vital for the efficient separation and disposal of radioactive materials Neidig, Clark, & Martin, 2013.

More Information

Product Name :4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononan-1-ol
CAS No. :80806-68-4Molecular Weight :378.13
MDL No. :MFCD00077578Purity/ Specification : 
Molecular Formula :C9H7F13OStorage :Sealed in dry,Room Temperature
Boiling Point :-  
GHS Pictogram : 
Signal Word :DangerPrecautionary Statements :P210-P233-P240-P241+P242+P243-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P403+P235-P501
UN# :1993Class :3
Hazard Statements :H225-H315-H319Packing Group :

 

download-icon
MS

download-icon
1HNMR

download-icon
CNMR

download-icon
IR1

download-icon
IR2

download-icon
Raman


 

)

Related products