Conditions | Yield |
---|---|
With xenon difluoride; silicon tetrafluoride at 90℃; for 13h; Fluorination; | 95% |
With nickel(II) fluoride; fluorine at 100℃; | 62% |
With AgFAsF6 In hydrogen fluoride at -196 - -70℃; for 0.0833333h; Yield given; | |
With cobalt (III) fluoride; Hexafluoroethane at 92℃; for 0.0333333h; Rate constant; Product distribution; var. time, var. temp.; | |
With fluorine at -20℃; under 1125.11 Torr; for 7.22222E-06h; |
Conditions | Yield |
---|---|
With fluorine; sodium fluoride at -100 - -10℃; for 12h; | A n/a B 84% |
Conditions | Yield |
---|---|
With xenon bis-pentafluoroseleniumoxide at 65℃; for 84h; | A 36% B n/a C 51% D 11% |
propane-1-sulfonamide
A
freon-218
B
Hexafluoroethane
C
ethanesulfonyl fluoride
D
1-perfluoropropanesulfonyl fluoride
Conditions | Yield |
---|---|
With hydrogen fluoride current: 4.5 to 5.5 V; 0.3 to 0.6 Adm-2; Further byproducts given; | A 2.8% B 3.1% C 4.3% D 40% |
acetone
A
freon-218
B
trifluoroacetyl fluoride
C
Hexafluoroacetone
Conditions | Yield |
---|---|
With copper; sodium fluoride at -100℃; | A n/a B n/a C 39% |
With copper; sodium fluoride at -100℃; Mechanism; | A n/a B n/a C 39% |
With copper; sodium fluoride at -100℃; |
C3F17IO2Te2
A
freon-218
B
1,1,1,2,2,3,3-heptafluoro-3-iodo-propane
C
C3F12OTe
Conditions | Yield |
---|---|
at 115℃; for 26h; | A n/a B n/a C 30% D n/a |
perfluoropropanesulfonic acid
A
fluorosulfonyl fluoride
B
Carbonyl fluoride
C
freon-218
D
perfluoropropanoyl fluoride
E
sulfur dioxide
Conditions | Yield |
---|---|
in Pt tube at 500°C, 1 h, incomplete reaction; | A n/a B n/a C 19% D 23% E n/a |
di-n-propylamine
A
freon-218
B
N,N-Difluor-heptafluor-n-propylamin
C
2,2,3,3,3-pentafluoro-N-(perfluoropropyl)propanimidoyl fluoride
D
F-(N-F-Fluoro,N,N-di-n-propylamine)
Conditions | Yield |
---|---|
With hydrogen fluoride at 7 - 8℃; Fluorination; Cleavage; Electrolysis; | A 20.1% B 1.3% C 1.8% D 7.8% |
With hydrogen fluoride at 7 - 8℃; for 10.9167h; Fluorination; Cleavage; Electrolysis; | A n/a B n/a C 1.9% D 6.2% |
trifluoromethan
A
polytetrafluoroethylene
B
carbon tetrafluoride
C
freon-218
D
perfluoropropylene
E
Hexafluoroethane
Conditions | Yield |
---|---|
With activated carbon supported potassium at 799.84℃; under 750.075 Torr; Pyrolysis; Inert atmosphere; | A 16.1% B n/a C n/a D 14.4% E n/a |
Conditions | Yield |
---|---|
With hydrogen fluoride at 7 - 8℃; for 6.55h; Fluorination; Cleavage; Electrolysis; | A n/a B 2.6% C 2.4% D 2.8% |
N-isopropylethylamine
A
freon-218
B
N,N-Difluor-heptafluorisopropylamin
C
perfluoro(4-methyl-3-aza-2-pentene)
Conditions | Yield |
---|---|
With hydrogen fluoride at 7 - 8℃; for 6.46667h; Fluorination; Cleavage; Electrolysis; Further byproducts given; | A n/a B n/a C 3.3 % Chromat. D 2.4% |
Conditions | Yield |
---|---|
bei der Zersetzung im elektrischen Lichtbogen; |
Conditions | Yield |
---|---|
im Kohlelichtbogen; | |
In neat (no solvent) other Radiation; decomposition of CF4 by (60)Co-γ-rays, formation of C2F6 and C3F8;; determination by ESR;; |
2,2,3-trichloro-1,1,1,3,3-pentafluoropropane
1,1,2,2-tetrachloro-1,3,3,3-tetrafluoropropane
A
freon-218
B
2-Chloro-F-propane
Conditions | Yield |
---|---|
With aluminum(III) fluoride; nitrogen; fluorine at 245 - 355℃; |
Conditions | Yield |
---|---|
With aluminum(III) fluoride; fluorine at 250℃; |
methane
freon-218
Conditions | Yield |
---|---|
With copper; fluorine |
Conditions | Yield |
---|---|
With antimony pentafluoride at 175℃; |
Conditions | Yield |
---|---|
With gold; fluorine at 150℃; | |
With boron trifluoride | |
With chlorine trifluoride at 100℃; | |
With antimony pentafluoride at 320℃; | |
With cobalt (III) fluoride at 400℃; |
Conditions | Yield |
---|---|
With fluorine at 275℃; |
Conditions | Yield |
---|---|
With hydrogen fluoride at -3℃; Electrolysis; |
Conditions | Yield |
---|---|
With copper; fluorine at 90℃; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
fluorodichloroacetyl fluoride
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
trichloroacetyl fluoride
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
difluoromalonyl difluoride
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
pentafluoroethyl oxyfluoride
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
1-fluoroxy 2-chlorotetrafluoroethane
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
1-fluoroxy 2,2-dichlorotrifluoroethane
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
1,1,1-Trichlor-2-fluoroxy-perfluoraethan
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
3-chlorotetrafluoropropionyl fluoride
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
trichloro-acetic acid-(3-hydroxy-propyl ester)
A
freon-218
B
trichlorofluoromethane
C
trifluoroacetyl fluoride
D
C3F8O2
Conditions | Yield |
---|---|
With fluorine; sodium fluoride Further byproducts given; |
Conditions | Yield |
---|---|
With cesium fluoride In N,N-dimethyl-formamide for 3h; | 95.1% |
freon-218
2H,2H-nonafluoro-1-iodo-3-methylbutane
A
2-Iodo-6-trifluoromethyl-5,5-dihydroperfluoroheptane
Conditions | Yield |
---|---|
at 200℃; for 48h; | A 71% B 7% |
Conditions | Yield |
---|---|
With hydrogen at 800℃; Pyrolysis; |
Conditions | Yield |
---|---|
With bromine at 850℃; |
The Perfluoropropane, with the CAS registry number 76-19-7 and EINECS registry number 200-941-9, has the systematic nane of octafluoropropane. It belongs to the product categories of Refrigerants and Organics. And the molecular formula of the chemical is C3F8.
The characteristics of Perfluoropropane are as followings: (1)ACD/LogP: 2.66; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.65; (4)ACD/LogD (pH 7.4): 2.65; (5)ACD/BCF (pH 5.5): 61.32; (6)ACD/BCF (pH 7.4): 61.32; (7)ACD/KOC (pH 5.5): 662.5; (8)ACD/KOC (pH 7.4): 662.5; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 0 Å2; (13)Index of Refraction: 1.221; (14)Molar Refractivity: 17.15 cm3; (15)Molar Volume: 121.7 cm3; (16)Polarizability: 6.8×10-24cm3; (17)Surface Tension: 9.3 dyne/cm; (18)Density: 1.543 g/cm3; (19)Enthalpy of Vaporization: 20.82 kJ/mol; (20)Vapour Pressure: 6250 mmHg at 25°C.
Perfluoropropane is a kind of colorless, odorless gas. And it is relatively inert. The mixture is nonflammable and nontoxic, though asphyxiation may occur because of displacement of oxygen. Exposure of the container to prolonged heat or fire can cause it to rupture violently and rocket.
Uses of Perfluoropropane: It can react with benzoyl fluoride to produce Heptafluoro-1-methylethyl-phenylketon. This reaction will need reagent CsF, and the menstruum dimethylformamide. The reaction time is 3 hours, and the yield is about 95.1%.
While dealing with this chemical, you had better take the following instructions: Keep container in a well-ventilated place, and do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer). What's more, if in case of insufficient ventilation, wear suitable respiratory equipment.
Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: FC(F)(F)C(F)(F)C(F)(F)F
(2)InChI: InChI=1/C3F8/c4-1(5,2(6,7)8)3(9,10)11
(3)InChIKey: QYSGYZVSCZSLHT-UHFFFAOYAL
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
dog | LD | intravenous | > 20mL/kg (20mL/kg) | International Journal of Toxicology. Vol. 17, Pg. 631, 1998. | |
monkey | LD | intravenous | > 20mL/kg (20mL/kg) | International Journal of Toxicology. Vol. 17, Pg. 631, 1998. | |
rabbit | LD | intramuscular | > 217uL/kg (0.217mL/kg) | BLOOD: HEMORRHAGE MUSCULOSKELETAL: OTHER CHANGES | International Journal of Toxicology. Vol. 17, Pg. 631, 1998. |
rat | LDLo | intravenous | 25mL/kg (25mL/kg) | BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) LUNGS, THORAX, OR RESPIRATION: DYSPNEA LUNGS, THORAX, OR RESPIRATION: CYANOSIS | International Journal of Toxicology. Vol. 17, Pg. 631, 1998. |
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