Product Name

  • Name

    Tetrafluorosilane

  • EINECS 232-015-5
  • CAS No. 7783-61-1
  • Article Data522
  • CAS DataBase
  • Density 1.209 g/cm3
  • Solubility
  • Melting Point -90°C
  • Formula F4Si
  • Boiling Point 86 °C
  • Molecular Weight 104.079
  • Flash Point
  • Transport Information UN 1859
  • Appearance COLOURLESS GAS , WITH PUNGENT ODOUR.
  • Safety 7/9-24/25-45-36/37/39-26-23
  • Risk Codes 26-35-34-31-26/27/28-14
  • Molecular Structure Molecular Structure of 7783-61-1 (Tetrafluorosilane)
  • Hazard Symbols CorrosiveC; ToxicT; VeryT+
  • Synonyms Siliconfluoride (SiF4) (8CI);Perfluorosilane;Silicontetrafluoride;Tetrafluorosilane;
  • PSA 0.00000
  • LogP 1.30000

Synthetic route

polytetrafluoroethylene
116-14-3

polytetrafluoroethylene

(1,1,2,2-tetrafluoroethyl)trifluorosilane
4168-07-4

(1,1,2,2-tetrafluoroethyl)trifluorosilane

A

pentafloropropylene
433-66-9

pentafloropropylene

B

1,1,2,2,3,3-Hexafluoro-cyclopropane
931-91-9

1,1,2,2,3,3-Hexafluoro-cyclopropane

C

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
379-14-6

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
at 150℃; for 18h; Further byproducts given;A 5%
B n/a
C 74%
D 100%
at 200℃; for 10h; Further byproducts given;A 19%
B n/a
C 71%
D 98%
(1,1,2,2-tetrafluoroethyl)trifluorosilane
4168-07-4

(1,1,2,2-tetrafluoroethyl)trifluorosilane

A

pentafloropropylene
433-66-9

pentafloropropylene

B

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
379-14-6

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

D

1,1,2-trifluoroethylene
359-11-5

1,1,2-trifluoroethylene

Conditions
ConditionsYield
With polytetrafluoroethylene at 150℃; for 18h; Further byproducts given;A 5%
B 74%
C 100%
D 10%
Carbonyl fluoride
353-50-4

Carbonyl fluoride

A

carbon dioxide
124-38-9

carbon dioxide

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) slight excess over the stoich. amt. of COF2 required; reaction mixt. heated in a stainless steel or monel cylinder at 160°C for 36 h;A n/a
B 100%
sodium hexafluorosilicate

sodium hexafluorosilicate

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) salt dried at 250°C in vac. or in N2 flow; thermal dissocn. at 500-620°C in vac. in stainless steel reactor; fed into metallic cylinder cooled with liq. N2; filtration, IR, atomic emission and mass spectrometry;100%
With water In neat (no solvent) byproducts: Si2OF6, SiF3OH, SiF3H; predrying of Na2SiF6 at 250-300.C in vac. or N2 for several hours, heating at 500 to 620°C in stainless steel reactor; cooling with liquid N2;
With sulfuric acid In sulfuric acid reaction by use of concd. H2SO4;;
(2,2-dichloro trifluoro ethyl) trifluoro silane
54939-02-5

(2,2-dichloro trifluoro ethyl) trifluoro silane

A

1,1'-dichloro-2,2'-difluoroethene
79-35-6

1,1'-dichloro-2,2'-difluoroethene

B

1,2-dichloro-1,2-difluoroethene
598-88-9

1,2-dichloro-1,2-difluoroethene

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) pyrolysis at 140°C, 3 hours;;A 8%
B 90%
C 100%
In neat (no solvent) pyrolysis at 140°C, 3 hours;;A 8%
B 90%
C 100%
diphenylfluorostibine
6651-55-4

diphenylfluorostibine

phenyltrifluorosilane
368-47-8

phenyltrifluorosilane

A

triphenylantimony
603-36-1

triphenylantimony

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
reflux for 3 d;A 100%
B n/a
reflux for 3 d;A 100%
B n/a
2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

(1,1,2,2-tetrafluoroethyl)trifluorosilane
4168-07-4

(1,1,2,2-tetrafluoroethyl)trifluorosilane

A

1-fluoro-1-difluoromethyl-2,2,3,3-tetramethylcyclopropane
17216-38-5

1-fluoro-1-difluoromethyl-2,2,3,3-tetramethylcyclopropane

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

C

1,1,2-trifluoroethylene
359-11-5

1,1,2-trifluoroethylene

Conditions
ConditionsYield
at 150℃; for 16h;A 86%
B 99%
C 6%
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
379-14-6

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane

cyclohexene
110-83-8

cyclohexene

A

polytetrafluoroethylene
116-14-3

polytetrafluoroethylene

B

pentafloropropylene
433-66-9

pentafloropropylene

C

carbon monoxide
201230-82-2

carbon monoxide

D

Octafluorocyclobutane
115-25-3

Octafluorocyclobutane

E

7,7-difluoronorcarane
823-70-1

7,7-difluoronorcarane

F

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
With Pyrex tube at 200℃; for 320h; Product distribution; Mechanism; further periods of contact time, other temperatures;A 14%
B 99%
C 11%
D n/a
E 47%
F 13%
polytetrafluoroethylene
116-14-3

polytetrafluoroethylene

(1,1,2,2-tetrafluoroethyl)trifluorosilane
4168-07-4

(1,1,2,2-tetrafluoroethyl)trifluorosilane

A

pentafloropropylene
433-66-9

pentafloropropylene

B

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
379-14-6

1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

D

1,1,2-trifluoroethylene
359-11-5

1,1,2-trifluoroethylene

Conditions
ConditionsYield
at 200℃; for 10h; Further byproducts given;A 19%
B 71%
C 98%
D 8%
phosgene
75-44-5

phosgene

sodium fluoride

sodium fluoride

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

fluoroformyl chloride
353-49-1

fluoroformyl chloride

C

carbon dioxide
124-38-9

carbon dioxide

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In acetonitrile condensation, 20°C in a sealed Pyrex tube, staying 24 h at 20°C;A 97%
B 0%
C n/a
D <1
Caesium-trans-bis(trifluormethyl)-tetrafluorphosphat
18114-91-5

Caesium-trans-bis(trifluormethyl)-tetrafluorphosphat

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
With glass; acid In not given97%
2-methyl-but-2-ene
513-35-9

2-methyl-but-2-ene

(1,1,2,2-tetrafluoroethyl)trifluorosilane
4168-07-4

(1,1,2,2-tetrafluoroethyl)trifluorosilane

A

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

B

1,1,2-trifluoroethylene
359-11-5

1,1,2-trifluoroethylene

1-fluoro-r-1-difluoromethyl-c-2,3-t-2-trimethylcyclopropane
17287-40-0, 17287-41-1, 74755-46-7, 74755-47-8

1-fluoro-r-1-difluoromethyl-c-2,3-t-2-trimethylcyclopropane

1-fluoro-r-1-difluoromethyl-c-2-t-2,3-trimethylcyclopropane
17287-40-0, 17287-41-1, 74755-46-7, 74755-47-8

1-fluoro-r-1-difluoromethyl-c-2-t-2,3-trimethylcyclopropane

Conditions
ConditionsYield
at 150℃; for 18h; Further byproducts given;A 96%
B 16%
C 34%
D 47%
diphenylfluorostibine
6651-55-4

diphenylfluorostibine

trichloromethyltrifluorosilane
1840-40-0

trichloromethyltrifluorosilane

A

diphenylantimony trichloride
21907-22-2

diphenylantimony trichloride

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
at 15°C;A n/a
B 90%
at 15°C;A n/a
B 90%
tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

N,N-dimethyl-n-octadecylamine
124-28-7

N,N-dimethyl-n-octadecylamine

Nonafluorobutanesulfonyl fluoride
375-72-4

Nonafluorobutanesulfonyl fluoride

A

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

B

N,N,N,-trimethyloctadecyl ammonium nonafluorobutanesulfonate
25628-14-2

N,N,N,-trimethyloctadecyl ammonium nonafluorobutanesulfonate

Conditions
ConditionsYield
In tetrahydrofuran 50°C , 6 h;A n/a
B 84%
In tetrahydrofuran 50°C , 6 h;A n/a
B 84%
antimony(III) fluoride
7783-56-4

antimony(III) fluoride

Dichlorosilane
4109-96-0

Dichlorosilane

A

difluorosilane
13824-36-7

difluorosilane

B

trifluorosilane
13465-71-9

trifluorosilane

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) byproducts: H2; reaction in presence of SbCl5 at room temperature;;A 80%
B n/a
C 10%
antimony(III) fluoride
7783-56-4

antimony(III) fluoride

Dichlorosilane
4109-96-0

Dichlorosilane

A

difluorosilane
13824-36-7

difluorosilane

B

hydrogen
1333-74-0

hydrogen

C

trifluorosilane
13465-71-9

trifluorosilane

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) fluorination of SiH2Cl2 with SbF3 at room temp. for a longer period of time;;A 80%
B n/a
C n/a
D n/a
disilicon hexafluoride
13830-68-7

disilicon hexafluoride

trimethylstannane
1631-73-8

trimethylstannane

A

F3SiSiH3
15195-26-3

F3SiSiH3

B

trimethyl(trifluorsilyl)stannane
126087-12-5

trimethyl(trifluorsilyl)stannane

C

trifluorosilane
13465-71-9

trifluorosilane

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

E

Trimethylstannylsilan
18365-37-2

Trimethylstannylsilan

Conditions
ConditionsYield
In neat (no solvent) N2 atmosphere, high vac. line; condensing, warming (room temp., 1.5 h); passing through traps (-78°C and -46°C);A n/a
B 77%
C n/a
D n/a
E 5%
stannous fluoride

stannous fluoride

silicon
7440-21-3

silicon

A

tin

tin

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In melt placing of mixt. of Si with SnF2 (molar ratio SnF2:Si=2.00) in Fluoroplast-4 ampule, closing by screwed stopper, exposition for 1.00 h at 250°C; various product ratio yields for various conditions; cooling, stirring up in water, collection, drying;A 76.8%
B n/a
hexafluorodisilthiane
41066-09-5

hexafluorodisilthiane

hydrogen bromide

hydrogen bromide

A

hexafluorodisiloxane

hexafluorodisiloxane

B

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) byproducts: CF3SiBr; under dry N2, in a sealed tube, 60 h at room temp., molar ratio of silane and HBr was 1:1, an other non-volatile product was also formed; fractionated distn. at a low-temp. column, S-compds. were trapped at 143K, SiF4 at 77 K;A n/a
B 68%
C 1%
iodo-bis-trifluoromethyl-arsine
359-55-7

iodo-bis-trifluoromethyl-arsine

silver fluoride

silver fluoride

A

bis(trifluoromethyl)fluoroarsine
359-54-6

bis(trifluoromethyl)fluoroarsine

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
with well dried AgF;A 60%
B n/a
with well dried AgF;A 60%
B n/a
potassium fluoride

potassium fluoride

disilicon hexabromide
13517-13-0

disilicon hexabromide

A

disilicon hexafluoride
13830-68-7

disilicon hexafluoride

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In 1,2-dichloro-ethane; acetonitrile Si2Cl6 dissolved in C2H4Cl2 added dropwise over 2 h to suspn. of KF in boiling MeCN, allowed to reflux for 30 min in slow stream of N2; gaseous products trapped in cooled (liq. N2) trap, anlyzed by IR;A 60%
B n/a
iodo-trifluoro-silane
16865-60-4

iodo-trifluoro-silane

HgS, red

HgS, red

A

hexafluorodisilthiane
41066-09-5

hexafluorodisilthiane

B

octafluorotrisildithiane

octafluorotrisildithiane

C

hexafluorodisiloxane
14515-39-0

hexafluorodisiloxane

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In neat (no solvent) byproducts: HgI2; CF3SiI:HgS molar ratio was 1:2, in a sealed tube, 300 K for 7 days, under dry N2; low temp. fractionated distn., less volatile fraction was purified by passing it through a 198 K trap into a trap held at 173 K, the (F3SiS)2SiF2 was identified by NMR, its purity was 98 %;;A 54%
B n/a
C 1%
D n/a
(1,2-dibromotrifluoroethyl)pentafluorosulfur(VI)
22687-88-3

(1,2-dibromotrifluoroethyl)pentafluorosulfur(VI)

A

fluorosulfonyl fluoride
640723-20-2, 2699-79-8, 12769-73-2

fluorosulfonyl fluoride

B

disulfur decafluoride
5714-22-7

disulfur decafluoride

C

1,2,2-tribromo-1,1,2-trifluoroethane
354-49-4

1,2,2-tribromo-1,1,2-trifluoroethane

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
Irradiation (UV/VIS); irradiated (Hanovia S 500 lamp) in silica ampule, 20 h, further products;A n/a
B n/a
C 49%
D n/a
E n/a
lithium aluminium tetrahydride
16853-85-3

lithium aluminium tetrahydride

SiF3SiHBr2
56144-86-6

SiF3SiHBr2

A

disilane

disilane

B

trifluorosilane
13465-71-9

trifluorosilane

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
React. occurs at room temp. (N2 or Ar, 15 min).; IR spectrum of volatile material indicates resulting compounds and 5% unreacted SiF3SiHBr2.;A 5%
B 45%
C 45%
potassium fluoride

potassium fluoride

hexachlorodisilane
13465-77-5

hexachlorodisilane

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

disilicon hexafluoride
13830-68-7

disilicon hexafluoride

C

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

Conditions
ConditionsYield
In 1,2-dichloro-ethane; acetonitrile Si2Cl6 dissolved in C2H4Cl2 added dropwise over 2 h to suspn. of KF in boiling MeCN, allowed to reflux for 30 min in slow stream of N2; gaseous products trapped in cooled (liq. N2) trap, analyzed by IR;A n/a
B 45%
C n/a
SiF3SiHBr2
56144-86-6

SiF3SiHBr2

i-Bu2AlH
1191-15-7

i-Bu2AlH

A

trifluorosilane
13465-71-9

trifluorosilane

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

C

monosilane
7440-21-3

monosilane

Conditions
ConditionsYield
In carbon dioxide; isopropyl alcohol; toluene Condensing of Si-compd. at -196°C, warming to -78°C (2-propanol/CO2), addn. of i-Bu2AlH (toluene) in portions over 30 min (N2 or Ar), warming of mixt. (room temp., 15 min).; Removal of volatile compounds under vac., IR identification.;A 40%
B 20%
C 40%
SiF3SiHBr2
56144-86-6

SiF3SiHBr2

Na(1+)*AlH2(1+)*2OCH2CH2OCH3(1-)=NaAlH2(OCH2CH2OCH3)2
22722-98-1

Na(1+)*AlH2(1+)*2OCH2CH2OCH3(1-)=NaAlH2(OCH2CH2OCH3)2

A

trifluorosilane
13465-71-9

trifluorosilane

B

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

C

monosilane
7440-21-3

monosilane

Conditions
ConditionsYield
In carbon dioxide; isopropyl alcohol; toluene Condensing of Si-compd. at -196°C, warming to -78°C (2-propanol/CO2), addn. of vitride (toluene) in portions over 30 min (N2 or Ar), warming of mixt. (room temp., 15 min).; Removal of volatile compounds under vac., IR identification.;A 40%
B 20%
C 40%
phosgene
75-44-5

phosgene

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

fluoroformyl chloride
353-49-1

fluoroformyl chloride

Conditions
ConditionsYield
excess of SiF4, heating up to 400°C in a quartz tube;100%
phosgene
75-44-5

phosgene

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

fluoroformyl chloride
353-49-1

fluoroformyl chloride

Conditions
ConditionsYield
In gaseous matrix molar ratio of educts 1:1, 400°C in a quartz tube;A 0%
B 100%
trimethyltin fluoride
420-60-0

trimethyltin fluoride

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

tris(trimethylstannyl)phosphane
10569-17-2

tris(trimethylstannyl)phosphane

A

B

[bis(2,4,6-triisopropylphenyl)SnPH]2

[bis(2,4,6-triisopropylphenyl)SnPH]2

Conditions
ConditionsYield
In tetrahydrofuran elem. anal., MAS;A 100%
B n/a
sodium aluminum tetrahydride

sodium aluminum tetrahydride

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

monosilane
7440-21-3

monosilane

Conditions
ConditionsYield
In diethylene glycol dimethyl ether byproducts: CH4; SiF4 was bubbled through soln. of NaAlH4 in diglyme at atmospheric pressure, heated at 0-60°C in He; chromy.; elem. anal.;99%
ethanol
64-17-5

ethanol

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

magnesium
7439-95-4

magnesium

A

magnesium fluoride

magnesium fluoride

B

tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

Conditions
ConditionsYield
Stage #1: ethanol; magnesium With iodine at 20℃; for 3.5h; Inert atmosphere; Reflux;
Stage #2: silicon tetrafluoride for 2.5h; Inert atmosphere; Reflux;
Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination;
A 98%
B 82%
methanol
67-56-1

methanol

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

magnesium
7439-95-4

magnesium

A

magnesium fluoride

magnesium fluoride

B

tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

Conditions
ConditionsYield
Stage #1: methanol; magnesium With iodine at 20℃; for 1.5h; Inert atmosphere; Reflux;
Stage #2: silicon tetrafluoride Inert atmosphere;
Stage #3: at 300℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature; Calcination;
A 98%
B 85%
Stage #1: methanol; magnesium at 20℃; for 3h;
Stage #2: silicon tetrafluoride at 20℃; for 0.5h; Temperature;
silicon tetrafluoride
7783-61-1

silicon tetrafluoride

A

ammonium hexafluorosilicate

ammonium hexafluorosilicate

B

tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

Conditions
ConditionsYield
With CH3OH; NH3 In methanol introduction of NH3 into CH3OH in absence of air; introduction of SiF4;; filtration; distn. of the filtrate;;A n/a
B 95%
With methanol; ammonia In methanol introduction of NH3 into CH3OH in absence of air; introduction of SiF4;; filtration; distn. of the filtrate;;A n/a
B 95%
silicon tetrafluoride
7783-61-1

silicon tetrafluoride

tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

Conditions
ConditionsYield
With C2H5OH SiF4 and C2H5OH in presence of NH3;;92%
With ethanol SiF4 and C2H5OH in presence of NH3;;92%
calcium hydride
7789-78-8

calcium hydride

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

monosilane
7440-21-3

monosilane

Conditions
ConditionsYield
With hydrogen In neat (no solvent) in flow reactor at 180°C; the diluent used was H2;90%
In neat (no solvent) Kinetics; byproducts: CaF2; mech. activated in rotating flow-through reactor; rotation frequency 100-150 rpm, CaF2 heated at temp. of 180-190°C, SiF4+H2 (1/1 v/v) flow through; gaseous products frozen out with liq. N2; detd. by gas-chromy.;

Silicon tetrafluoride Consensus Reports

Reported in EPA TSCA Inventory.

Silicon tetrafluoride Standards and Recommendations

OSHA PEL: TWA 2.5 mg(F)/m3
ACGIH TLV: TWA 2.5 mg(F)/m3; BEI: 3 mg/g creatinine of fluorides in urine prior to shift; 10 mg/g creatinine of fluorides in urine at end of shift.
NIOSH REL: (Inorganic Fluorides) TWA 2.5 mg(F)/m3
DOT Classification:  2.3; Label: Poison Gas, Corrosive

Silicon tetrafluoride Specification

The CAS registry number of Silicon tetrafluoride is 7783-61-1. The IUPAC name is tetrafluorosilane. Its EINECS registry number is 232-015-5. In addition, the molecular formula is F4Si and the molecular weight is 104.08. This tetrahedral molecule is notable for having a remarkably narrow liquid range (its boiling point is only 4 °C above its melting point).

Physical properties about this chemical are: (1)ACD/LogP: 4.15; (2)ACD/LogD (pH 5.5): 4.15; (3)ACD/LogD (pH 7.4): 4.15; (4)ACD/BCF (pH 5.5): 837.56; (5)ACD/BCF (pH 7.4): 837.56; (6)#Freely Rotating Bonds: 0; (7)Polar Surface Area: 0 Å2; (8)Index of Refraction: 1.207; (9)Molar Refractivity: 11.42 cm3; (10)Molar Volume: 86 cm3; (11)Polarizability: 4.52 ×10-24cm3; (12)Surface Tension: 5.1 dyne/cm; (13)Density: 1.209 g/cm3; (14)Enthalpy of Vaporization: 17.05 kJ/mol; (15)Vapour Pressure: 26400 mmHg at 25°C.

Preparation of Silicon tetrafluoride: it is a by-product of the production of phosphate fertilizers, resulting from the attack of HF(derived from fluorapatite protonolysis) on silicates. It is prepared by heating BaSiF6(>300 °C). In addition, the required BaSiF6 is prepared by treating aqueous hexafluorosilicic acid with barium chloride.

Uses of Silicon tetrafluoride: it can be used to get fluorine silicate and fluoride lead. And it can be used as a stiffening agent of cement and artificial marble, also used for synthetic materials of organic silicon compounds.

When you are using this chemical, please be cautious about it as the following:
This chemical can react violently with water and can cause severe burns. If it contact with acids, it will liberate toxic gas. And it is very Toxic by inhalation, in contact with skin and if swallowed. During using it, wear suitable protective clothing, gloves and eye/face protection and avoid contact with skin and eyes. In case of accident or if you feel unwell, seek medical advice immediately (show label where possible). After using it, keep container tightly closed and in a well-ventilated place.

You can still convert the following datas into molecular structure:
(1)SMILES: F[Si](F)(F)F
(2)InChI: InChI=1/F4Si/c1-5(2,3)4
(3)InChIKey: ABTOQLMXBSRXSM-UHFFFAOYAU

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rat LC50 inhalation 2272ppm (2272ppm) SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE

LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Journal of Toxicological Sciences. Vol. 18, Pg. 394, 1993.

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