1651-41-8

  • Product Name:3-(Perfluorooctyl)Propanol
  • MF:C11H7 F17 O
  • Purity:99%
  • Molecular Weight:478.149
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Product Details

Cost-effective customized wholesale 3-(Perfluorooctyl)Propanol 1651-41-8

  • Molecular Formula:C11H7 F17 O
  • Molecular Weight:478.149
  • Melting Point:42 °C 
  • Boiling Point:196.7°Cat760mmHg 
  • PKA:14.84±0.10(Predicted) 
  • Flash Point:72.8°C 
  • PSA:20.23000 
  • Density:1.59g/cm3 
  • LogP:5.76830 

1651-41-8 Relevant articles

Synthesis and antimicrobial activity of a perfluoroalkyl-containing quaternary ammonium salt

Shao, Hui,Jiang, Li,Meng, Wei-Dong,Qing, Feng-Ling

, p. 89 - 91 (2003)

A novel perfluoroalkyl-containing quater...

Synthesis and surface antimicrobial activity of a novel perfluorooctylated quaternary ammonium silane coupling agent

Shao, Hui,Meng, Wei-Dong,Qing, Feng-Ling

, p. 721 - 724 (2004)

A novel perfluorooctyl-containing quater...

Fluorous biphasic catalysis. 2. Synthesis of fluoroponytailed amine ligands along with fluoroponytailed carboxylate synthons, [M(C8F17(CH2)2CO2) 2] (M = Mn2+ or Co2+)

Vincent,Rabion,Yachandra,Fish

, p. 888 - 895 (2001)

Fluorous biphasic catalysis (FBC) is a r...

A convenient access to triarylphosphines with fluorous phase affinity

Sinou, Denis,Pozzi, Gianluca,Hope, Eric G.,Stuart, Alison M.

, p. 849 - 852 (1999)

Perfluorocarbon-soluble triarylphosphine...

Copper(I) complexes mediated cyclization reaction of unsaturated ester under fluoro biphasic procedure

De Campo, Floryan,Lastecoueres, Dominique,Vincent, Jean-Marc,Verlhac, Jean-Baptiste

, p. 4969 - 4971 (1999)

-

Synthesis of 3-perfluoroalkyl-propyl esters of L-(+)-tartaric acid

Szlavik, Zoltan,Tarkanyi, Gabor,Tarczay, Gyoergy,Goemoery, Agnes,Rabai, Jozsef

, p. 83 - 87 (1999)

A convenient and effective method for th...

Syntheses of fluorous propenes from 3-perfluoroalkyl-2-iodo-1-propanols

Szíjjártó, Csongor,Ivanko, Peter,Takács, Ferenc T.,Szabó, Dénes,Rábai, József

, p. 386 - 389 (2008)

3-(Perfluoroalkyl)-1-propenes are obtain...

Self-assembled monolayers on gold generated from terminally perfluorinated alkanethiols bearing propyl vs. ethyl hydrocarbon spacers

Zenasni, Oussama,Jamison, Andrew C.,Marquez, Maria D.,Lee, T. Randall

, p. 128 - 136 (2015/03/05)

This paper examines the structural and i...

Mesophase structure of low-wetting liquid crystalline polyacrylates with new perfluoroalkyl benzoate side groups

Martinelli, Elisa,Paoli, Francesca,Gallot, Bernard,Galli, Giancarlo

experimental part, p. 4128 - 4139 (2011/10/30)

The synthesis, thermal behavior, bulk mi...

Br?nsted acidic imidazolium salts containing perfluoroalkyl tails catalyzed one-pot synthesis of 1,8-dioxo-decahydroacridines in water

Shen, Wei,Wang, Li-Min,Tian, He,Tang, Jun,Yu, Jian-jun

body text, p. 522 - 527 (2009/11/30)

One-pot three-component synthesis of 1,8...

Towards oligosaccharide library synthesis by fluorous mixture method

Tojino, Mami,Mizuno, Mamoru

scheme or table, p. 5920 - 5923 (2009/04/05)

The synthesis of an oligosaccharide libr...

1651-41-8 Process route

C<sub>31</sub>H<sub>29</sub>F<sub>17</sub>O<sub>11</sub>

C31H29F17O11

2,3,4,6-tetra-O-acetyl-α/β-D-galactopyranose
3947-62-4,6207-76-7,10343-06-3,19235-21-3,22554-70-7,22860-22-6,57884-82-9,62057-79-8,70191-05-8,109525-54-4,140147-37-1,47339-09-3

2,3,4,6-tetra-O-acetyl-α/β-D-galactopyranose

4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol
1651-41-8

4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol

Conditions
Conditions Yield
With ammonium cerium (IV) nitrate; In MeCN; water; at 20 ℃; for 2.5h;
78%
64%
3-perfluoro-n-octyl-2-iodo-1-propanol
38550-45-7

3-perfluoro-n-octyl-2-iodo-1-propanol

4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol
1651-41-8

4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol

Conditions
Conditions Yield
With tri-n-butyl-tin hydride;
88%
With tri-n-butyl-tin hydride; In toluene; for 8h; Heating;
80%
With hydrazine hydrate; nickel; In methanol; at 0 - 10 ℃; for 2h;
78%
With lithium aluminium tetrahydride; In tetrahydrofuran;
76%
With tri-n-butyl-tin hydride; In various solvent(s);
75%
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In various solvent(s); at 80 ℃; for 4h;
75%
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; at 80 ℃; for 24h;
75%
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; at 80 ℃; for 24h;
70%
3-perfluoro-n-octyl-2-iodo-1-propanol; With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; Inert atmosphere;
With water; sodium hydroxide; In diethyl ether;
45%
With nickel; hydrazine hydrate; In methanol; at 0 - 10 ℃; for 2h;
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; at 60 - 85 ℃; for 12.25h;

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