134052-02-1

Basic information

• Product Name: 1H,1H,2H,2H,3H,3H,4H,4H,5H,5H-PERFLUOROUNDECAN-1-OL
• Synonyms: 1H,1H,2H,2H,3H,3H,4H,4H,5H,5H-PERFLUOROUNDECAN-1-OL;5-(Perfluorohexyl)pentan-1-ol;6,6,7,7,8,8,9,9,10,10,11,11,11-Tridecafluoroundecan-1-ol
• CAS NO: 134052-02-1
• Molecular Formula: C₁₁H₁₁F₁₃O
• Molecular Weight: 406.18
• Mol File: 134052-02-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H,1H,2H,2H,3H,3H,4H,4H,5H,5H-PERFLUOROUNDECAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 1H,1H,2H,2H,3H,3H,4H,4H,5H,5H-PERFLUOROUNDECAN-1-OL(134052-02-1)
• EPA Substance Registry System: 1H,1H,2H,2H,3H,3H,4H,4H,5H,5H-PERFLUOROUNDECAN-1-OL(134052-02-1)

Safety Data

• Hazardous Substances Data: 134052-02-1(Hazardous Substances Data)

Usage

Molecular Structure

A chain of 11 carbon atoms with all hydrogen atoms replaced by fluorine atoms.

Chemical Family

Perfluorinated compounds.

Designation

"1H,1H,2H,2H,3H,3H,4H,4H,5H,5H" indicates the positions of the hydrogen atoms in the molecule.

Usage

Commonly used as a surfactant in various industrial and consumer products.

Applications

Surface coatings, lubricants, firefighting foams, electronics, and semiconductor industries.

Unique Chemical Properties

Thermal and chemical stability, water and oil repellency.

Environmental Concerns

Persistence in the environment and potential health effects leading to regulatory restrictions in some countries.

Upstream product

• 821-09-0 n-Pent-4-enyl alcohol 
• 355-43-1 n-perfluorohexyl iodide 
• 132665-00-0 5-(F-hexyl)-4-iodopentanol 
• 1576-85-8 4-pentenyl acetate 
• 3003-84-7 Tetrahydrofurfuryl chloride 
• 145193-77-7 5-(n-perfluorohexyl)-4-iodo-pentylacetate 

Downstream Products

• 900159-45-7 toluene-4-sulfonic acid 6,6,7,7,8,8,9,9,10,10,11,11,11-tridecanfluoro-undecyl ester 

Relevant articles and documents

Hetero Diels-Alder cyclocondensation of F-alkyl aldehydes with the Danishefsky diene

The heterocyclocondensation of F-alkylated aldehydes R(F)(CH2)(n)CHO with Danishefsky's diene depends on the mutual vicinity of the carbonyl and the F-alkyl chain: when n=4 it leads to 4-oxo pyr-2-ene 4, but when n=O the trimethylsilyloxypyrene 3 without methoxy elimination only results.

Synthesis and structure-activity relationship (SAR) of novel perfluoroalkyl-containing quaternary ammonium salts

A new series of perfluoroalkyl-containing quaternary ammonium compounds were prepared and examined for their antibacterial activities. The perfluoroalkyl-containing quaternary ammonium salts mainly exhibited excellent antibacterial activity for the Gram-p

Synthese d'acides ω perfluoroalkylalcanoiques et d'ω perfluoroalkylalcanols

The simple and effective syntheses of acids and alcohols of general formula CnF2n+1(CH2)mY (Y=CO2H, CH2OH; n=6,8 and m=4,5) have been described.

Addition of perfluoroalkyl iodides to 4-pentenol and its derivatives: one-pot preparation of 2--tetrahydrofurans

Dependimg on the nature of the lakaline medium, the radical addition of perfluoroalkyl iodides to 4-pentenol gives a mixture of 5-(F-alkyl)-4-pentenol and 2-tetrahydrofuran, or the latter alone.