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307-24-4 Usage

Chemical Properties

Perfluorohexanoic acid (PFHxA) exists as a colourless liquid, it is insoluble in water. Perfluorohexanoic acid has the ability to react with strong oxidizing agents. Upon decomposition, PFHxA can form carbon oxides and hydrogen fluoride. Additional information related to the physical and chemical properties of PFHxA are not currently available.

Uses

Different sources of media describe the Uses of 307-24-4 differently. You can refer to the following data:
1. Perfluorohexanoic acid (PFHxA, perfluorocaproic acid, undecafluorohexanoic acid, undecafluoro-1-hexanoic Acid) is a six-carbon compound in the perfluoroalkyl family of chemicals. Perfluorohexanoic acid is used in stain- and grease-proof coatings on furniture, carpet, and food packaging. Perfluorohexanoic acid is the six-carbon version of the highly persistent and outlawed PFOA. Much like other perfluoroalkyls, PFHxA can persist in the environment.
2. Undecafluorohexanoic acid, a volatile ion-pair reagent, has been used as mobile phase for LC-MS analysis of highly polar sulfonium pseudo-sugar constituents neosalacinol and neokotalanol, potential α-glucosidase inhibitors isolated from ayurvedic traditional medicine Salacia species.

Definition

ChEBI: A monocarboxylic acid that is perfluorinated hexanoic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 307-24-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 307-24:
(5*3)+(4*0)+(3*7)+(2*2)+(1*4)=44
44 % 10 = 4
So 307-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C6HF11O2/c7-2(8,1(18)19)3(9,10)4(11,12)5(13,14)6(15,16)17/h(H,18,19)

307-24-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • TCI America

  • (U0067)  Undecafluorohexanoic Acid  >98.0%(T)

  • 307-24-4

  • 5g

  • 850.00CNY

  • Detail
  • TCI America

  • (U0067)  Undecafluorohexanoic Acid  >98.0%(T)

  • 307-24-4

  • 25g

  • 2,490.00CNY

  • Detail
  • Aldrich

  • (29226)  Undecafluorohexanoicacid  ≥97.0% (T)

  • 307-24-4

  • 29226-5ML

  • 2,322.45CNY

  • Detail

307-24-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name perfluorohexanoic acid

1.2 Other means of identification

Product number -
Other names IPC-PFFA-6

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:307-24-4 SDS

307-24-4Synthetic route

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

perfluorohexyl sulfinic acid

perfluorohexyl sulfinic acid

Conditions
ConditionsYield
With sulfur dioxide In water; N,N-dimethyl-formamide at 20℃; Product distribution; effect of water content of the solvent, role of allyl alcohol, Faradic yield;A 3%
B 95%
sodium undecafluorohexanoate
2923-26-4

sodium undecafluorohexanoate

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With sulfuric acid at 120℃;94%
perfluoro-2-octene
65500-50-7

perfluoro-2-octene

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With bis(acetylacetonate)oxovanadium; dihydrogen peroxide92%
With bis(acetylacetonate)oxovanadium; dihydrogen peroxide Product distribution; various reaction conditions;92%
n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

allyl bromide
106-95-6

allyl bromide

A

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane
355-37-3

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane

B

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

C

3-(perfluorohexyl)prop-1-ene
80793-18-6

3-(perfluorohexyl)prop-1-ene

Conditions
ConditionsYield
With potassium hydroxide; 2,2'-azobis(isobutyronitrile) at 80℃; for 56h; Substitution;A n/a
B n/a
C 88%
n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; lipoxygenase; oct-2-yne at 25 - 30℃;84%
With ammonium peroxydisulfate; sodium formate In N,N-dimethyl-formamide at 55℃; for 12h;83.9%
Multi-step reaction with 2 steps
1: 79 percent / sodium formaldehyde sulfoxylate, NaHCO3 / dimethylformamide; H2O / 17 h / 80 - 85 °C
2: 94 percent / concentrated sulfuric acid / 120 °C
View Scheme
(E)-perfluorooct-2-ene
31143-13-2

(E)-perfluorooct-2-ene

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With hydrogen; oxygen; lead(II) oxide; ozone; calcium carbonate; palladium In 1,1,2-Trichloro-1,2,2-trifluoroethane 1.) 5 deg C to 10 deg C, 2 h, 2.) 20 deg C;80%
allyl iodid
556-56-9

allyl iodid

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane
355-37-3

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane

B

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

C

3-(perfluorohexyl)prop-1-ene
80793-18-6

3-(perfluorohexyl)prop-1-ene

Conditions
ConditionsYield
With potassium hydroxide; 2,2'-azobis(isobutyronitrile) at 80℃; for 56h; Substitution;A n/a
B n/a
C 77%
sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
102061-83-6

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With 2,2'-azobis(2-methylpropionamidine) dihydrochloride; water at 55℃; for 6.5h;75%
sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
102061-83-6

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate

allyl-trimethyl-silane
762-72-1

allyl-trimethyl-silane

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-(trimethylsilyl)nonane
132673-95-1

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-(trimethylsilyl)nonane

Conditions
ConditionsYield
With ammonium peroxydisulfate In N,N-dimethyl-formamide at 40℃; for 4h;A 13%
B 74%
sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
102061-83-6

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate

allyl bromide
106-95-6

allyl bromide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

3-(perfluorohexyl)prop-1-ene
80793-18-6

3-(perfluorohexyl)prop-1-ene

Conditions
ConditionsYield
With ammonium peroxydisulfate In N,N-dimethyl-formamide at 40℃; for 4h;A 12%
B 67%
1-Phenylprop-1-yne
673-32-5

1-Phenylprop-1-yne

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

1-phenyl-2-(perfluorohexyl)propene
113999-57-8

1-phenyl-2-(perfluorohexyl)propene

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; catalase at 25 - 30℃; for 504h;A 66%
B 28%
n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

phenylacetylene
536-74-3

phenylacetylene

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

(E)-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-octen-1-yl)benzene
55009-92-2, 113999-56-7

(E)-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-octen-1-yl)benzene

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; urease at 25 - 30℃; for 264h;A 2%
B 66%
Allyl acetate
591-87-7

Allyl acetate

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
102061-83-6

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononyl acetate
83311-03-9

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluorononyl acetate

Conditions
ConditionsYield
With ammonium peroxydisulfate In N,N-dimethyl-formamide at 40℃; for 4h;A 24%
B 63%
n-octyne
629-05-0

n-octyne

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

(E)-1-(perfluorohexyl)-1-octene
113999-58-9

(E)-1-(perfluorohexyl)-1-octene

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; catalase at 25 - 30℃; for 312h;A 14%
B 61%
sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate
102061-83-6

sodium 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfinate

propargyl bromide
106-96-7

propargyl bromide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1,2-nonadiene
130716-18-6

4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1,2-nonadiene

Conditions
ConditionsYield
With ammonium peroxydisulfate In N,N-dimethyl-formamide at 40℃; for 4h;A 17%
B 54%
oct-2-yne
2809-67-8

oct-2-yne

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

2-(perfluorohexyl)-2-octene
113999-59-0

2-(perfluorohexyl)-2-octene

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; urease at 25 - 30℃; for 720h;A 53%
B 18%
1-decyne
764-93-2

1-decyne

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-7-hexadecene
120464-27-9

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-7-hexadecene

Conditions
ConditionsYield
With disodium hydrogenphosphate; potassium dihydrogenphosphate; urease at 25 - 30℃;A 39%
B 42%
n-hexanoic anhydride
2051-49-2

n-hexanoic anhydride

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
With hydrogen fluoride anschliessend Behandeln mit Wasser;
undecafluorohexanoyl chloride
335-53-5

undecafluorohexanoyl chloride

silver(I) cyanide
506-64-9

silver(I) cyanide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

hydroxy-undecafluoropentyl-malonic acid diamide
595-06-2

hydroxy-undecafluoropentyl-malonic acid diamide

Conditions
ConditionsYield
Behandeln des als ein Dimeres des Undecafluor-2-oxo-hexannitrils angesehenen Reaktionsprodukts mit konz.wss.Salzsaeure;
hexanoic acid
142-62-1

hexanoic acid

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
anodische Fluorierung;
perfluorohexyl fluorosulfate
67097-65-8

perfluorohexyl fluorosulfate

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
(hydrolysis);
(E)-1,1,1,2,2,3,3,4,5,6,6,7,7,8,8,9,9,9-Octadecafluoro-non-4-ene

(E)-1,1,1,2,2,3,3,4,5,6,6,7,7,8,8,9,9,9-Octadecafluoro-non-4-ene

A

heptafluorobutyric Acid
375-22-4

heptafluorobutyric Acid

B

pentafluoropropionic acid
422-64-0

pentafluoropropionic acid

C

Perfluoropentanoic acid
2706-90-3

Perfluoropentanoic acid

D

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

E

perfluoroheptanoic acid
375-85-9

perfluoroheptanoic acid

F

trifluoroacetic acid
76-05-1

trifluoroacetic acid

Conditions
ConditionsYield
With ruthenium(IV) oxide; sodium hypochlorite; ruthenium tetroxide In 1,1,2-Trichloro-1,2,2-trifluoroethane for 1h; Product distribution; other times, other reagents, other times, further products;
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanoic acid
53826-12-3

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanoic acid

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

2-Dimethylamino-methylen-1,3-bis-dimethyl-immonio-propan
45084-94-4

2-Dimethylamino-methylen-1,3-bis-dimethyl-immonio-propan

C

Dimethyl-<3-dimethylamino-prop-2t-en-yliden>ammonium
38571-88-9, 52950-91-1, 80077-94-7

Dimethyl-<3-dimethylamino-prop-2t-en-yliden>ammonium

Conditions
ConditionsYield
With trichlorophosphate at 60 - 85℃; Vilsmeier reaction;
Perfluorooctanoic acid
335-67-1

Perfluorooctanoic acid

A

heptafluorobutyric Acid
375-22-4

heptafluorobutyric Acid

B

Perfluoropentanoic acid
2706-90-3

Perfluoropentanoic acid

C

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

D

perfluoroheptanoic acid
375-85-9

perfluoroheptanoic acid

Conditions
ConditionsYield
With sodium sulfate; Ni-Cu photocatalyst; titanium(IV) oxide In water for 2h; Kinetics; UV-irradiation; Electrochemical reaction;
With sulfuric acid; LaNi0.8Sr0.2O3; iron(II) sulfate; sodium sulfate In water for 2.5h; pH=5; Catalytic behavior; Kinetics; Mechanism; Reagent/catalyst; pH-value; Electrolysis;
1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane
335-56-8

1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 84 percent / sodium formaldehyde sulfoxylate, NaHCO3 / dimethylformamide; H2O / 20 h / 80 - 85 °C
2: 94 percent / concentrated sulfuric acid / 120 °C
View Scheme
1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane
355-37-3

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: KSO3F / fluorosulfonic acid / (electrolysis)
2: (hydrolysis)
View Scheme
perfluorohexanoyl cyanide dimer

perfluorohexanoyl cyanide dimer

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

Conditions
ConditionsYield
hydrolysis;
perfluoroheptanoic acid
375-85-9

perfluoroheptanoic acid

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
With dipotassium peroxodisulfate; water at 60℃; under 4875.49 Torr; for 3h; Kinetics; Temperature; Reagent/catalyst;
Perfluorooctanoic acid
335-67-1

Perfluorooctanoic acid

A

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

B

perfluoroheptanoic acid
375-85-9

perfluoroheptanoic acid

Conditions
ConditionsYield
for 4h; Electrolysis;
Perfluorooctanoic acid
335-67-1

Perfluorooctanoic acid

A

1H-perfluoropentane
375-61-1

1H-perfluoropentane

B

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane
355-37-3

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane

C

Perfluoropentanoic acid
2706-90-3

Perfluoropentanoic acid

D

perfluoro-1H-heptane
375-83-7

perfluoro-1H-heptane

E

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

F

perfluoroheptanoic acid
375-85-9

perfluoroheptanoic acid

Conditions
ConditionsYield
With water at 23 - 51℃; for 0.025h; Microwave irradiation; Sonication;
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

N-aminoethyl(perfluoropentyl)formylamine

N-aminoethyl(perfluoropentyl)formylamine

Conditions
ConditionsYield
at 30 - 132℃; for 0.5h;96.7%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

isopropyl alcohol
67-63-0

isopropyl alcohol

isopropyl 2,2,3,3,4,4,5,5,6,6,6-undecafluorohexanoate

isopropyl 2,2,3,3,4,4,5,5,6,6,6-undecafluorohexanoate

Conditions
ConditionsYield
for 3h; Reflux;90%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

perfluoro-n-hexyl chloride
355-41-9

perfluoro-n-hexyl chloride

Conditions
ConditionsYield
With trichlorophosphate at 5 - 110℃;90%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

1,3-adamantandiol
5001-18-3

1,3-adamantandiol

3-hydroxy-1-adamantyl perfluorohexanoate
1005454-12-5

3-hydroxy-1-adamantyl perfluorohexanoate

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 4h; Heating / reflux;88%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

methylmagnesium bromide
75-16-1

methylmagnesium bromide

3,3,4,4,5,5,6,6,7,7,7-undecafluoroheptan-2-one
2708-07-8

3,3,4,4,5,5,6,6,7,7,7-undecafluoroheptan-2-one

Conditions
ConditionsYield
Stage #1: undecafluorohexanoic acid; methylmagnesium bromide In diethyl ether at -8 - 20℃; for 2h; Inert atmosphere;
Stage #2: With hydrogenchloride In water
64%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

palladium diacetate
3375-31-3

palladium diacetate

palladium perfluorohexanoate

palladium perfluorohexanoate

Conditions
ConditionsYield
In 1-methyl-pyrrolidin-2-one at 60℃; for 24h; Inert atmosphere;61%
tert.-butylhydroperoxide
75-91-2

tert.-butylhydroperoxide

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

palladium diacetate
3375-31-3

palladium diacetate

palladium (II) tert-butyl peroxide perfluorohexanoate

palladium (II) tert-butyl peroxide perfluorohexanoate

Conditions
ConditionsYield
In neat (no solvent) byproducts: C5F11CO2H; mixed with stirring at room temp.; filtered, washed (n-pentane), dried (vac.), elem. anal.;60%
palladium (II) nitrate

palladium (II) nitrate

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

palladium perfluorohexanoate

palladium perfluorohexanoate

Conditions
ConditionsYield
at 80℃; for 12h; Inert atmosphere;57%
3-methanesulfonyloxy-1-adamantyl methacrylate
861675-46-9

3-methanesulfonyloxy-1-adamantyl methacrylate

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

3-[(perfluoropentyl)carbonyloxy]-1-adamantyl methacrylate
1005454-11-4

3-[(perfluoropentyl)carbonyloxy]-1-adamantyl methacrylate

Conditions
ConditionsYield
With sodium dihydrogenphosphate; 4-methoxy-phenol In 4-butanolide at 120℃; for 6h; Product distribution / selectivity;51.5%
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

copper (I) tert-butoxide
35342-67-7, 35342-68-8

copper (I) tert-butoxide

[(1,10-phenanthroline)2Cu][n-C5F11CO2]

[(1,10-phenanthroline)2Cu][n-C5F11CO2]

Conditions
ConditionsYield
Stage #1: 1,10-Phenanthroline; copper (I) tert-butoxide In tetrahydrofuran at 20℃; for 0.0833333h;
Stage #2: undecafluorohexanoic acid In tetrahydrofuran at 20℃; for 0.333333h;
51%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

palladium dichloride

palladium dichloride

palladium perfluorohexanoate

palladium perfluorohexanoate

Conditions
ConditionsYield
at 100℃; for 2h; Inert atmosphere;46%
undecafluorohexanoic acid
307-24-4

undecafluorohexanoic acid

palladium(II) hydroxide

palladium(II) hydroxide

palladium perfluorohexanoate

palladium perfluorohexanoate

Conditions
ConditionsYield
at 80℃; for 12h; Inert atmosphere;42%

307-24-4Relevant articles and documents

Patton, R. H.,Simons, J. H.

, p. 2016 - 2017 (1955)

SYNTHESE D'ACIDES PERFLUOROALCANE CARBOXYLIQUE ET SULFINIQUE PAR REDUCTION ELECTROCHIMIQUE D'IODURES DE PERFLUOROALKYLE SUR CATHODE EN FIBRES DE CARBONE DANS LE SOLVANT N,N-DIMETHYLFORMAMIDE. APPLICATION A LA SYNTHESE DE PERFLUORO α,ο DIACIDES

Benefice-Malouet, Sylvie,Blancou, Hubert,Calas, Patrick,Commeyras, Auguste

, p. 125 - 140 (1988)

The electrochemical reduction of C6F13I on a carbon fibre cathode in DMF as solvent and in the presence of SO2 is studied.Depending on the water content of the solvent, perfluorohexyl sulfinic acid C6F13SO2H or perfluoropentyl carboxylic acid C5F11COOH are obtained.These reactions are applied to 1,4-diiodoperfluorobutane; by varying the composition of the solvent it has been possible to obtain the two diacidic compounds : HO2S(CF2)4SO2H and HO2S(CF2)3COOH.

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Germain,A.,Commeyras,A.

, p. 118 - 119 (1978)

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Electrocatalytic degradation of perfluorooctanoic acid by LaNixY1-xO3 (Y = Fe, Cu, Co, Sr) gas dispersion electrode

Chen, Yongyang,Guo, Dan,Dong, Xiaochun,Li, Yahui,Huang, Yixuan,Chen, Hao,Li, Shanping

, (2020/12/23)

Perfluorooctanoic acid (PFOA), as a refractory organic pollutant, seriously harms the environment and damages human health. Here, the electrocatalytic method was selected to degrade PFOA. In this work, perovskite catalysts doped with different elements, and corresponding gas diffusion electrodes (GDE) were prepared by the gel-sol method and citric acid complexation method. The crystal structure, microscopic morphology, and electrochemical properties of the LaNixY1-xO3 (Y = Fe, Cu, Co, Sr) perovskite catalyst electrode were analyzed by XRD, TEM, and CV. Moreover, the electrocatalytic performances of the as-prepared electrodes were assessed by the degradation of PFOA, and the Sr-doped GDE exhibited the highest degradation rate of PFOA. The optimum degradation conditions, such as the current density, pH, and initial concentration were also investigated. It was observed that when the current density was 20 mA/cm2, pH was 5, and initial concentration was 0.25 mmol/L, the Sr-doped GDE had the best degradation and defluorination efficiency of PFOA reached 90.0 % and 75.1 %, respectively. High performance liquid chromatography-mass spectrometry (HPLC-MS) was used to analyze the intermediate products of PFOA degradation and obtain the degradation pathway. With the combined action of [rad]OH and O2, PFOA was degraded by stepwise removal of CF2 groups, which were ultimately degraded into F? and CO2.

The effect of oxygen in the photocatalytic oxidation pathways of perfluorooctanoic acid

Sansotera, Maurizio,Persico, Federico,Rizzi, Valentina,Panzeri, Walter,Pirola, Carlo,Bianchi, Claudia L.,Mele, Andrea,Navarrini, Walter

, p. 159 - 168 (2015/11/10)

The influence of oxygen in the photocatalytic oxidation of perfluorooctanoic acid (PFOA) promoted by a commercial nano-sized titanium dioxide was studied by testing the reaction in different conditions: static air, oxygen flux, nitrogen flux and pre-saturated nitrogen flux. The reaction was monitored by Total Organic Carbon (TOC) analysis and Ionic Chromatography (IC). Shorter chain perfluorocarboxylic acids (PFCAs; Cn, n = 1-7) intermediate degradation products were quantitatively determined by High-Performance Liquid Chromatography combined with Mass Spectrometry (HPLC-MS) analysis. The presence of shorter chain PFCAs in solution was also monitored by 19F NMR. The experimental findings are in agreement with two major oxidative pathways: Cn → Cn-1 photo-redox and β-scissions routes mediated by COF2 elimination. Depending on the experimental conditions, the mutually operating mechanisms could be unbalanced up to the complete predominance of one pathway over the other. In particular, the existence of the β-scissions route with COF2 elimination was corroborated by the isolation and characterization of carbonyl difluoride, a predicted fluorinated decomposition by-product.

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