Perfluoro(2-methyl-3-pentanone) supplier

Name
Perfluoro(2-methyl-3-pentanone)
EINECS 436-710-6
CAS No. 756-13-8
Article Data21
CAS DataBase
Density 1.66g/cm³
Solubility 24-332.6mg/L at 25℃
Melting Point -108ºC
Formula C₆F₁₂O
Boiling Point 60°C at 760mmHg
Molecular Weight 316.046
Flash Point 9.1°C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols Xi
Synonyms 3-Pentanone, 1,1,1,2,2,4,5,5,5-nonafluoro-4-(trifluoromethyl)-;
PSA 17.07000
LogP 3.58600

Synthetic route

: 116-15-4
perfluoropropylene

: 422-61-7
perfluoropropanoyl fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With iron(III) trifluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave;	98.2%
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 95℃; under 1875.19 Torr;
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 788-67-0
1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2,3-epoxypentane

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
In diethylene glycol at 60℃; for 2h; Temperature; Reagent/catalyst; Autoclave;	97.8%
With triethylamine In acetonitrile at 30℃; for 0.166667h; Temperature; Reagent/catalyst; Solvent; Time;	97.1%
With sodium fluoride In 1,2-dimethoxyethane at 20℃; for 9h;	94%

: 116-14-3
polytetrafluoroethylene

: 677-84-9
perfluoroisobutyryl fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With iron(III) trifluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave;	96.8%
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 788-50-1, 73041-04-0, 117642-62-3
trans-2,3-epoxyperfluoro-4-methylpentane

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In 1,2-dimethoxyethane at 50℃; for 9h;	92%

: 75677-98-4
2,3-bi(fluorosulfato)perfluoro-4-methylpentane

A: 422-64-0
pentafluoropropionic acid

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In N,N-dimethyl-formamide at 20℃; for 4h;	A 76% B 16%

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 2062-98-8, 125037-08-3
perfluoro(2-propoxypropionyl) fluoride

B: 359-72-8
perfluoro-2-methyl-2-pentene

C: 756-13-8
perfluoro-2-methylpentan-3-one

D: 287101-12-6
perfluoro-4-methylpent-1-ene

Conditions

Conditions	Yield
With potassium fluoride In diethylene glycol dimethyl ether	A 9.7% B n/a C 63.5% D 18%

...Expand

: 1584-03-8
perfluoro-2-methylpent-2-ene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 93 percent / sodium hypochlorite / H2O; acetonitrile 2: 94 percent / NaF / 1,2-dimethoxy-ethane / 9 h / 20 °C View Scheme
Multi-step reaction with 2 steps 1: sodium hypochlorite; urea / acetonitrile; water / 3 h / 20 °C 2: potassium fluoride; 18-crown-6 ether / diethylene glycol dimethyl ether / 3 h / 30 °C View Scheme

: 3709-71-5
trans-perfluoro-(4-methyl-2-pentene)

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 70 percent / sodium hypochlorite / H2O; acetonitrile 2: antimony pentafluoride / 2.5 h / 250 °C View Scheme
Multi-step reaction with 2 steps 1: 70 percent / sodium hypochlorite / H2O; acetonitrile 2: 92 percent / CsF / 1,2-dimethoxy-ethane / 9 h / 50 °C View Scheme

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Stage #1: Hexafluoropropene oxide With potassium fluoride In diethylene glycol dimethyl ether for 2h; Heating; Stage #2: perfluoropropylene In diethylene glycol dimethyl ether; acetonitrile at 65 - 80℃; under 5250.53 Torr; for 2h;
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 422-61-7
perfluoropropanoyl fluoride

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 130℃; Reagent/catalyst; Temperature;

...Expand

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 2062-98-8, 125037-08-3
perfluoro(2-propoxypropionyl) fluoride

B: 422-61-7
perfluoropropanoyl fluoride

C: 756-13-8
perfluoro-2-methylpentan-3-one

D: 287101-12-6
perfluoro-4-methylpent-1-ene

Conditions

Conditions	Yield
With activated carbon BAU In neat (no solvent) at 130℃; Reagent/catalyst; Temperature;

...Expand

: 2070-70-4
perfluoro-4-methyl-2-pentene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: sulfolane; cesium fluoride / diethylene glycol dimethyl ether / 0.5 h / 70 °C 2: sodium hypochlorite; urea / acetonitrile; water / 3 h / 20 °C 3: potassium fluoride; 18-crown-6 ether / diethylene glycol dimethyl ether / 3 h / 30 °C View Scheme
Multi-step reaction with 3 steps 1: benzyltriethylammonium bromide; potassium fluoride / acetonitrile / 4 h 2: sodium hypochlorite / diethylene glycol dimethyl ether / 4 h 3: Aliquat 336 / diethylene glycol dimethyl ether / 10 h View Scheme

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 116-15-4
perfluoropropylene

B: 422-61-7
perfluoropropanoyl fluoride

Conditions

Conditions	Yield
With cesium fluoride at 250℃; for 2h; Product distribution;	A 68% B n/a

: 756-13-8
perfluoro-2-methylpentan-3-one

: 87383-00-4
3-hydroperfluoro-2-methyl-3-pentanol

Conditions

Conditions	Yield
Stage #1: perfluoro-2-methylpentan-3-one With polyethylsiloxane; tetrabutoxytitanium at 100℃; Stage #2: With sodium hydroxide In tetrahydrofuran Heating;	42%
With sodium tetrahydroborate In 1,4-dioxane for 1h;

: 75-38-7
Vinylidene fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

: 18329-56-1
1-<2-Trifluormethyl-perfluorpentyl-(3)-oxy>-1,1-difluor-2-brom-aethan

Conditions

Conditions	Yield
(i) CsF, MeCN, (ii) /BRN= 1733321/, Br2; Multistep reaction;

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

B: 422-64-0
pentafluoropropionic acid

Conditions

Conditions	Yield
With sodium hydroxide In water Product distribution;	A 92 % Chromat. B 85 % Chromat.

: 756-13-8
perfluoro-2-methylpentan-3-one

: 77-78-1
dimethyl sulfate

: 132182-92-4
1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-pentane

Conditions

Conditions	Yield
With potassium fluoride In diethylene glycol dimethyl ether at 45℃;

: 123-75-1
pyrrolidine

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 686720-34-3
N-tetramethyleneperfluoropropanamide

B: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

C: 309-24-0
N-butyl pentafluoropropionamide

Conditions

Conditions	Yield
With freon 11

...Expand

: 116-15-4
perfluoropropylene

: 422-61-7
perfluoropropanoyl fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With iron(III) trifluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave;	98.2%
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 95℃; under 1875.19 Torr;
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 788-67-0
1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2,3-epoxypentane

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
In diethylene glycol at 60℃; for 2h; Temperature; Reagent/catalyst; Autoclave;	97.8%
With triethylamine In acetonitrile at 30℃; for 0.166667h; Temperature; Reagent/catalyst; Solvent; Time;	97.1%
With sodium fluoride In 1,2-dimethoxyethane at 20℃; for 9h;	94%

: 116-14-3
polytetrafluoroethylene

: 677-84-9
perfluoroisobutyryl fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With iron(III) trifluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave;	96.8%
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 788-50-1, 73041-04-0, 117642-62-3
trans-2,3-epoxyperfluoro-4-methylpentane

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In 1,2-dimethoxyethane at 50℃; for 9h;	92%

: 75677-98-4
2,3-bi(fluorosulfato)perfluoro-4-methylpentane

A: 422-64-0
pentafluoropropionic acid

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In N,N-dimethyl-formamide at 20℃; for 4h;	A 76% B 16%

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 2062-98-8, 125037-08-3
perfluoro(2-propoxypropionyl) fluoride

B: 359-72-8
perfluoro-2-methyl-2-pentene

C: 756-13-8
perfluoro-2-methylpentan-3-one

D: 287101-12-6
perfluoro-4-methylpent-1-ene

Conditions

Conditions	Yield
With potassium fluoride In diethylene glycol dimethyl ether	A 9.7% B n/a C 63.5% D 18%

...Expand

: 30320-26-4
1,1,1,4,5,5,5-heptafluoro-3-(pentafluoroethyl)-2,4-bis(trifluoromethyl)pent-2-ene

A: 756-13-8
perfluoro-2-methylpentan-3-one

B: 2,2-bis(fluorosulfonyloxy)perfluoropropane

Conditions

Conditions	Yield
With bis(fluorosulfuryl) peroxide at 80℃; for 192h;	A 61% B 49%
With bis(fluorosulfuryl) peroxide at 70 - 80℃;

: 788-67-0
1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2,3-epoxypentane

A: 756-13-8
perfluoro-2-methylpentan-3-one

B: 83714-48-1
2-chloroundecafluoro-2-methyl-3-pentanone

Conditions

Conditions	Yield
With sodium chloride In diethylene glycol dimethyl ether for 20h; Heating;	A 35% B 55.8%

: 83714-48-1
2-chloroundecafluoro-2-methyl-3-pentanone

A: 116-15-4
perfluoropropylene

B: 422-61-7
perfluoropropanoyl fluoride

C: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In diethylene glycol dimethyl ether for 1h; Product distribution; Heating;	A n/a B n/a C 38%

...Expand

: 788-67-0
1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2,3-epoxypentane

: 57-13-6
urea

A: 756-13-8
perfluoro-2-methylpentan-3-one

B: 1315483-13-6
1-(2,2,3,3,3-pentafluoropropionyl)-3-(2,2,2-trifluoro-1-trifluoromethylethyl)urea

Conditions

Conditions	Yield
In acetonitrile for 17h; Heating; Sealed tube;	A n/a B 25%

...Expand

: 788-50-1
perfluoro(4-methyl-2-pentene) oxide

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In diethylene glycol dimethyl ether

: 788-50-1
perfluoro(4-methyl-2-pentene) oxide

A: 68970-43-4
perfluoro(2,4-dimethyloxolane)

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With antimony pentafluoride at 200℃; for 10h; Yield given. Yields of byproduct given;

: 132182-90-2
2,3-bis(fluorosulfato)perfluoro-(2-methylpentane)

A: 677-71-4
hexafluoroacetone hydrate

B: 422-64-0
pentafluoropropionic acid

C: 756-13-8
perfluoro-2-methylpentan-3-one

D: 788-67-0
1,1,1,3,4,4,5,5,5-nonafluoro-2-trifluoromethyl-2,3-epoxypentane

Conditions

Conditions	Yield
With cesium fluoride In N,N-dimethyl-formamide at 10℃; for 1h; Yield given;	A n/a B n/a C 1.5 g D 0.3 g
With cesium fluoride In N,N-dimethyl-formamide at 10℃; for 1h;	A n/a B n/a C 1.5 g D 0.3 g

...Expand

: 788-50-1, 73041-04-0, 117642-62-3
trans-2,3-epoxyperfluoro-4-methylpentane

A: 73041-05-1
perfluoro(4-methyl-2-pentanone)

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With antimony pentafluoride at 250℃; for 2.5h; Yield given. Yields of byproduct given;

: 103697-21-8
2,3-epoxyperfluoro-3-isopropyl-4-methylpentane

A: 116-15-4
perfluoropropylene

B: 1584-03-8
perfluoro-2-methylpent-2-ene

C: 30320-29-7
1,1,1,2,3,5,5,6,6,7,7,7-dodecafluoro-2,4-bis(trifluoromethyl)hept-3-ene

D: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With cesium fluoride In diethylene glycol dimethyl ether for 2h; Heating; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;	A 0.8 g B n/a C n/a D n/a
With cesium fluoride In diethylene glycol dimethyl ether for 2h; Heating; Yield given. Further byproducts given. Title compound not separated from byproducts;	A 0.8 g B n/a C n/a D n/a

...Expand

: 1584-03-8
perfluoro-2-methylpent-2-ene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 93 percent / sodium hypochlorite / H2O; acetonitrile 2: 94 percent / NaF / 1,2-dimethoxy-ethane / 9 h / 20 °C View Scheme
Multi-step reaction with 2 steps 1: sodium hypochlorite; urea / acetonitrile; water / 3 h / 20 °C 2: potassium fluoride; 18-crown-6 ether / diethylene glycol dimethyl ether / 3 h / 30 °C View Scheme

: 3709-71-5
trans-perfluoro-(4-methyl-2-pentene)

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 70 percent / sodium hypochlorite / H2O; acetonitrile 2: antimony pentafluoride / 2.5 h / 250 °C View Scheme
Multi-step reaction with 2 steps 1: 70 percent / sodium hypochlorite / H2O; acetonitrile 2: 92 percent / CsF / 1,2-dimethoxy-ethane / 9 h / 50 °C View Scheme

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Stage #1: Hexafluoropropene oxide With potassium fluoride In diethylene glycol dimethyl ether for 2h; Heating; Stage #2: perfluoropropylene In diethylene glycol dimethyl ether; acetonitrile at 65 - 80℃; under 5250.53 Torr; for 2h;
at 160℃; under 750.075 Torr; for 10h; Gas phase;

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 422-61-7
perfluoropropanoyl fluoride

B: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 130℃; Reagent/catalyst; Temperature;

...Expand

: 428-59-1
Hexafluoropropene oxide

: 116-15-4
perfluoropropylene

A: 2062-98-8, 125037-08-3
perfluoro(2-propoxypropionyl) fluoride

B: 422-61-7
perfluoropropanoyl fluoride

C: 756-13-8
perfluoro-2-methylpentan-3-one

D: 287101-12-6
perfluoro-4-methylpent-1-ene

Conditions

Conditions	Yield
With activated carbon BAU In neat (no solvent) at 130℃; Reagent/catalyst; Temperature;

...Expand

: 2070-70-4
perfluoro-4-methyl-2-pentene

: 756-13-8
perfluoro-2-methylpentan-3-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: sulfolane; cesium fluoride / diethylene glycol dimethyl ether / 0.5 h / 70 °C 2: sodium hypochlorite; urea / acetonitrile; water / 3 h / 20 °C 3: potassium fluoride; 18-crown-6 ether / diethylene glycol dimethyl ether / 3 h / 30 °C View Scheme
Multi-step reaction with 3 steps 1: benzyltriethylammonium bromide; potassium fluoride / acetonitrile / 4 h 2: sodium hypochlorite / diethylene glycol dimethyl ether / 4 h 3: Aliquat 336 / diethylene glycol dimethyl ether / 10 h View Scheme

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 116-15-4
perfluoropropylene

B: 422-61-7
perfluoropropanoyl fluoride

Conditions

Conditions	Yield
With cesium fluoride at 250℃; for 2h; Product distribution;	A 68% B n/a

: 756-13-8
perfluoro-2-methylpentan-3-one

: 87383-00-4
1,1,1,2,2,4,5,5,5-nonafluoro-4-(trifluoromethyl)pentanol

Conditions

Conditions	Yield
Stage #1: perfluoro-2-methylpentan-3-one With polyethylsiloxane; tetrabutoxytitanium at 100℃; Stage #2: With sodium hydroxide In tetrahydrofuran Heating;	42%
With sodium tetrahydroborate In 1,4-dioxane for 1h;
With sodium tetrahydroborate at 0℃; for 1.5h;

: 75-38-7
Vinylidene fluoride

: 756-13-8
perfluoro-2-methylpentan-3-one

: 18329-56-1
1-<2-Trifluormethyl-perfluorpentyl-(3)-oxy>-1,1-difluor-2-brom-aethan

Conditions

Conditions	Yield
(i) CsF, MeCN, (ii) /BRN= 1733321/, Br2; Multistep reaction;

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

B: 422-64-0
pentafluoropropionic acid

Conditions

Conditions	Yield
With sodium hydroxide In water Product distribution;	A 92 % Chromat. B 85 % Chromat.

: 756-13-8
perfluoro-2-methylpentan-3-one

: 77-78-1
dimethyl sulfate

: 132182-92-4
1,1,1,2,2,3,4,5,5,5-decafluoro-3-methoxy-4-(trifluoromethyl)-pentane

Conditions

Conditions	Yield
With potassium fluoride In diethylene glycol dimethyl ether at 45℃;

: 123-75-1
pyrrolidine

: 756-13-8
perfluoro-2-methylpentan-3-one

A: 686720-34-3
N-tetramethyleneperfluoropropanamide

B: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

C: 309-24-0
N-butyl pentafluoropropionamide

Conditions

Conditions	Yield
With freon 11

...Expand

: 756-13-8
perfluoro-2-methylpentan-3-one

: 109-89-7
diethylamine

A: 21016-40-0
C9H12F5NO

B: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

C: 10186-77-3
N-Diethyl-pentafluor-propionsaeureamid

D: ethylamine pentafluoropropionate

Conditions

Conditions	Yield
With freon 11

...Expand

: 756-13-8
perfluoro-2-methylpentan-3-one

: 109-73-9
N-butylamine

A: 431-89-0
1,1,1,2,3,3,3-Heptafluoropropane

B: 4853-56-9
(butylidene)butylamine

C: 309-24-0
N-butyl pentafluoropropionamide

Conditions

Conditions	Yield
With freon 11

...Expand

: 756-13-8
perfluoro-2-methylpentan-3-one

: 422-64-0
pentafluoropropionic acid

Conditions

Conditions	Yield
With water pH=8 - 14;

Perfluoro(2-methyl-3-pentanone) Specification

The cas register number of Perfluoro(2-methyl-3-pentanone) is 756-13-8. It also can be called as 1,1,1,2,2,4,5,5,5-Nonafluoro-4-(trifluoromethyl)pentan-3-one and the Systematic name about this chemical is 3-Pentanone, 1,1,1,2,2,4,5,5,5-nonafluoro-4-(trifluoromethyl)-.

Physical properties about Perfluoro(2-methyl-3-pentanone) are: (1)ACD/LogP: 8.24; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 8.24; (4)ACD/LogD (pH 7.4): 8.24; (5)ACD/BCF (pH 5.5): 1000000; (6)ACD/BCF (pH 7.4): 1000000; (7)ACD/KOC (pH 5.5): 721085; (8)ACD/KOC (pH 7.4): 721085; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 17.07Å²; (13)Index of Refraction: 1.264; (14)Molar Refractivity: 31.66 cm³; (15)Molar Volume: 190.3 cm³; (16)Surface Tension: 13.6 dyne/cm; (17)Density: 1.66 g/cm³; (18)Flash Point: 9.1 °C; (19)Enthalpy of Vaporization: 30.25 kJ/mol; (20)Boiling Point: 60 °C at 760 mmHg; (21)Vapour Pressure: 196 mmHg at 25°C.

People can use the following data to convert to the molecule structure.
1.SMILES: FC(F)(F)C(F)(C(=O)C(F)(F)C(F)(F)F)C(F)(F)F
2.InChI: InChI=1/C6F12O/c7-2(4(10,11)12,5(13,14)15)1(19)3(8,9)6(16,17)18
3.InChIKey: RMLFHPWPTXWZNJ-UHFFFAOYAW
4.Std. InChI: InChI=1S/C6F12O/c7-2(4(10,11)12,5(13,14)15)1(19)3(8,9)6(16,17)18

Product Name

Perfluoro(2-methyl-3-pentanone)

Synthetic route

Perfluoro(2-methyl-3-pentanone) Specification

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