6-(Perfluorohexyl)hexanol

Base Information

Chemical Name:6-(Perfluorohexyl)hexanol
CAS No.:161981-35-7
Molecular Formula:C12H13 F13 O
Molecular Weight:420.214
Hs Code.:2905190098
DSSTox Substance ID:DTXSID50379859
Nikkaji Number:J3.453.606F
Wikidata:Q81985832
Mol file:161981-35-7.mol

Synonyms:6-(Perfluorohexyl)hexanol;161981-35-7;7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluorododecan-1-ol;1-Dodecanol, 7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluoro-;SCHEMBL1194348;DTXSID50379859;6-(Tridecafluorohexyl)-1-hexanol;7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluoro-dodecan-1-ol;MFCD00153241;FT-0620827;A810319

Suppliers and Price of 6-(Perfluorohexyl)hexanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

SynQuest Laboratories
6-(Perfluorohexyl)hexan-1-ol 96%
5 g
$ 450.00

SynQuest Laboratories
6-(Perfluorohexyl)hexan-1-ol 96%
1 g
$ 150.00

American Custom Chemicals Corporation
6-(PERFLUOROHEXYL)HEXANOL 95.00%
5G
$ 1549.89

Total 11 raw suppliers

Chemical Property of 6-(Perfluorohexyl)hexanol

Chemical Property:

Vapor Pressure:0.00928mmHg at 25°C
Refractive Index:1.353
Boiling Point:235.2°Cat760mmHg
Flash Point:96°C
PSA：20.23000
Density:1.423g/cm³
LogP:5.66800
XLogP3:6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:10
Exact Mass:420.0758811
Heavy Atom Count:26
Complexity:455

Purity/Quality:

97% ^*data from raw suppliers

6-(Perfluorohexyl)hexan-1-ol 96% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:F
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:

Useful:

Canonical SMILES:C(CCCO)CCC(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F

Technology Process of 6-(Perfluorohexyl)hexanol

There total 6 articles about 6-(Perfluorohexyl)hexanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 177722-97-3
7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluoro-5-iodododecan-1-ol

: 161981-35-7
7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluorododecan-1-ol

Guidance literature:: With zinc; In ethanol; at 50 ℃; for 4h;

Reference yield: 34.0%

: 109-99-9,24979-97-3,77392-70-2
tetrahydrofuran

: 821-41-0
5-Hexen-1-ol

: 335-56-8
1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane

: C₁₆H₁₉F₁₃O₂

: 161981-35-7
7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluorododecan-1-ol

Guidance literature:: With Eosin Y; water; sodium thiosulfate; In acetonitrile; at 20 ℃; for 17h; Inert atmosphere; Irradiation;
DOI:10.1021/acs.orglett.8b03596

Reference yield:

: 821-41-0
5-Hexen-1-ol

: 161981-35-7
7,7,8,8,9,9,10,10,11,11,12,12,12-tridecafluorododecan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / AIBN / 80 °C

2: 74 percent / H₂; diethylamine / 5 percent Pd/C / ethanol; ethyl acetate / 0.5 h / 9120 Torr

With 2,2'-azobis(isobutyronitrile); hydrogen; diethylamine; palladium on activated charcoal; In ethanol; ethyl acetate; 1: Addition / 2: Reduction;
DOI:10.1016/S0022-1139(99)00078-0