Product Name

  • Name

    Thionyl fluoride

  • EINECS 231-997-2
  • CAS No. 7783-42-8
  • Article Data123
  • CAS DataBase
  • Density 1.758 g/cm3
  • Solubility Hydrolysis in water, soluble in ethanol and benzene
  • Melting Point -129 °C
  • Formula F2OS
  • Boiling Point -43.8 °C
  • Molecular Weight 86.0622
  • Flash Point
  • Transport Information
  • Appearance Colorless gas
  • Safety 36/37/39-45
  • Risk Codes 20-34
  • Molecular Structure Molecular Structure of 7783-42-8 (Thionyl fluoride)
  • Hazard Symbols CorrosiveC,FlammableF,ToxicT
  • Synonyms Sulfurdifluoride monoxide;Sulfur difluoride oxide;Sulfur fluoride oxide (SF2O);Sulfur oxide fluoride (SOF2);Sulfur oxyfluoride (SOF2);Sulfurous oxyfluoride;Thionyl difluoride;
  • PSA 36.28000
  • LogP 1.36980

Synthetic route

vanadium pentafluoride
7783-72-4, 44247-54-3

vanadium pentafluoride

sulfur dioxide
7446-09-5

sulfur dioxide

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: VOF3; vigorous react.;97.8%
thionyl chloride
7719-09-7

thionyl chloride

fluorine
7782-41-4

fluorine

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In further solvent(s) fluorination (N2 carrier gas (ratio F/N2 1:5), -50°C, als solvent freon-11);80%
In neat (no solvent) at 0°C under inflammation (pale blue); further oxifluoride formed;;
(trifluoroethenyl)pentafluorosulfur(VI)
1186-51-2

(trifluoroethenyl)pentafluorosulfur(VI)

A

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

fluorosulfonyl fluoride

B

bis(pentafluorosulfur)oxide
42310-84-9

bis(pentafluorosulfur)oxide

C

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

D

difluoro(pentafluorosulfanyl)acetyl fluoride
54555-26-9

difluoro(pentafluorosulfanyl)acetyl fluoride

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
With oxygen 25°C, 12 h, further product;A n/a
B n/a
C n/a
D 72%
E n/a
With O2 25°C, 12 h, further product;A n/a
B n/a
C n/a
D 72%
E n/a
With ozone 25°C, 12 h, further product;A n/a
B n/a
C n/a
D 52%
E n/a
With O3 25°C, 12 h, further product;A n/a
B n/a
C n/a
D 52%
E 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
thionyl chloride
7719-09-7

thionyl chloride

1,2,2,2-tetrafluoro-ethanesulfonyl fluoride
2127-74-4

1,2,2,2-tetrafluoro-ethanesulfonyl fluoride

triethylamine
121-44-8

triethylamine

A

thionyl chlorofluoride
14177-25-4

thionyl chlorofluoride

B

1-chlorotetrafluoroethanesulfonyl chloride
25221-39-0

1-chlorotetrafluoroethanesulfonyl chloride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
-70°C;A n/a
B 47%
C n/a
-70°C;A n/a
B 47%
C n/a
chlorine fluorosulfate
13997-90-5

chlorine fluorosulfate

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

A

SF4(Cl)OSO2F
88548-62-3, 88588-20-9

SF4(Cl)OSO2F

B

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In neat (no solvent) ClOSO2F transferred under static vac. to FEP reactor, SF4 condensed andreactor placed in 0°C bath and left for 1.5 h; reactor cooled to -95°C, volatile materials pumped from -95 to -70°C, reactor allowed to warm to room temp., volatile materials pumped into -196°C trap and fractionated, product refractionated through -63°C trap;A 46%
B n/a
bis(pentafluorosulfur) peroxide
12395-41-4

bis(pentafluorosulfur) peroxide

sulfur dioxide
7446-09-5

sulfur dioxide

A

thionyl tetrafluoride
173009-97-7, 118492-84-5, 13709-54-1

thionyl tetrafluoride

B

pentafluorosulfur fluorosulfonate
81439-35-2

pentafluorosulfur fluorosulfonate

C

sulfur trioxide
7446-11-9

sulfur trioxide

D

thionyl fluoride
7783-42-8

thionyl fluoride

E

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
byproducts: SiF4, sulfur; other Radiation; photochemical reaction with 253.7 nm radiation, 48 h;A n/a
B 45%
C n/a
D n/a
E n/a
thiocyanogen
505-14-6

thiocyanogen

fluorine
7782-41-4

fluorine

A

thiazyl trifluoride
15930-75-3

thiazyl trifluoride

B

sulphur cyanide pentafluoride
1512-13-6

sulphur cyanide pentafluoride

C

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

D

thionyl fluoride
7783-42-8

thionyl fluoride

E

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
In further solvent(s) byproducts: (FCN)3; reactn. of a soln. of dirhodane in FCl2C-CClF2 with diluted F2 (F2:N2 0 1:10); cooled down to -183°C; solvent removed by condensation; mixt. condensed to aq. KOH-soln. at room temp. to remove SF4, SOF and (FCN)3; sepn. by fractionated condensation at -127°C, -140°C, -196°C;A 8%
B 5%
C 30%
D 40%
E 3%
nitrogen trifluoride
7783-54-2

nitrogen trifluoride

sulfur trioxide
7446-11-9

sulfur trioxide

A

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

fluorosulfonyl fluoride

B

2NO(1+)*S2O5F4(2-)=(NO)2S2O5F4

2NO(1+)*S2O5F4(2-)=(NO)2S2O5F4

C

thionyl fluoride
7783-42-8

thionyl fluoride

D

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
byproducts: NO, NO2; 520 °C, nickel tube;A 30%
B n/a
C 4%
D <1
potassium fluoride

potassium fluoride

S8(2+)*2AsF6(1-) = S8(AsF6)2

S8(2+)*2AsF6(1-) = S8(AsF6)2

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In liquid sulphur dioxide15%
N-(pentafluorosulfanyl)-(dichloro)methanimide
1801-00-9

N-(pentafluorosulfanyl)-(dichloro)methanimide

A

Schwefelpentafluorid-isocyanid
804533-76-4

Schwefelpentafluorid-isocyanid

B

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
With P(i-Pr)3 In neat (no solvent) byproducts: 2-fluoro-propane, SOF2; all manipulations in dry evacuated apparatus; S and P compds. added through septum into liq. N2 cooled apparatus; trap at -196°C contained F5SNC, other compds. in trap at -120°C;A 10%
B n/a
With tris(2-octyl) phosphite In neat (no solvent) byproducts: SOF2; all manipulations in dry evacuated apparatus under Ar; S and P compds. added through septum into liq. N2 cooled apparatus then allowed to warm very slowly with stirring; trap at -196°C contained F5SNC, other compds. in trap at -100°C and -78°C;
thionyl chloride
7719-09-7

thionyl chloride

thiazyl trifluoride
15930-75-3

thiazyl trifluoride

hydrogen fluoride
7664-39-3

hydrogen fluoride

A

SF5N=SCl2
25502-15-2

SF5N=SCl2

B

((pentafluorosulfanyl)imino)chlorofluorosulfane
80997-19-9

((pentafluorosulfanyl)imino)chlorofluorosulfane

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
HF and NSF3 were condesed in Kel-F reactor at -196°C, allowed toreact at room temp. overnight, SOCl2 added, reacted at room temp. for 2weeks and volatile products were condensed into a NaF scrubber; fractionation through a series of traps at -10, -78, and -196°C in vac., a -78°C trap contained the product, distillation;A 9.6%
B <1
C n/a
HF and NSF3 were condesed in steel cylinder at -196°C, allowed to react at room temp. for 1 h, SOCl2 added, heated at 79°C for 24h and volatile products were condensed into a NaF scrubber; fractionation through a series of traps at -10, -78, and -196°C in vac., a -78°C trap contained the product, distillation;A 2%
B n/a
C n/a
dinitrogen difluoride
10578-16-2

dinitrogen difluoride

sulfur dioxide
7446-09-5

sulfur dioxide

A

fluorosulfonyl anhydride
13036-75-4

fluorosulfonyl anhydride

B

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

fluorosulfonyl fluoride

C

thionyl tetrafluoride
173009-97-7, 118492-84-5, 13709-54-1

thionyl tetrafluoride

D

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: N2O, N2;
dinitrogen difluoride
10578-16-2

dinitrogen difluoride

sulfur dioxide
7446-09-5

sulfur dioxide

A

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

fluorosulfonyl fluoride

B

fluorosulfonylchloride
13637-84-8

fluorosulfonylchloride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
With chlorin byproducts: S2O5F2, SOF4, N2O, N2; 100°C, 1.5 h, in autoclave;
dinitrogen difluoride
10578-16-2

dinitrogen difluoride

sulfur dioxide
7446-09-5

sulfur dioxide

A

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

fluorosulfonyl fluoride

B

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: S2O5F2, SOF4, N2O, N2; 100°C, 1.5 h, in autoclave;
hypofluorous acid trifluoromethyl ester
373-91-1

hypofluorous acid trifluoromethyl ester

sulfur dioxide
7446-09-5

sulfur dioxide

A

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

fluorosulfonyl fluoride

B

Trifluormethyl-fluordisulfat

Trifluormethyl-fluordisulfat

C

Bis-(trifluormethyl)-sulfat
1479-52-3

Bis-(trifluormethyl)-sulfat

D

trifluoromethanesulfonyl hypofluorite

trifluoromethanesulfonyl hypofluorite

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: CO2; 170-180°C, further products; fractionated distn.;
difluoroether
7783-41-7

difluoroether

hydrogen sulfide
7783-06-4

hydrogen sulfide

A

sulfur
7704-34-9

sulfur

B

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: S, HF; 12 h, room temp.;
byproducts: S, HF; 12 h, room temp.;
sodium thiosulfate

sodium thiosulfate

A

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

fluorosulfonyl fluoride

B

sodium fluoride

sodium fluoride

C

sodium sulfate
7757-82-6

sodium sulfate

D

thionyl fluoride
7783-42-8

thionyl fluoride

E

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
With fluorine byproducts: O2; -80°C;
With F2 byproducts: O2; -80°C;
sulfur dioxide
7446-09-5

sulfur dioxide

tetramethylammonium fluoride
373-68-2

tetramethylammonium fluoride

nitrosonium tetrafluoroborate

nitrosonium tetrafluoroborate

A

nitrogen
7727-37-9

nitrogen

B

fluorosulfate(1-)

fluorosulfate(1-)

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In liquid sulphur dioxide
In sulfur dioxide
sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

sulfur dioxide
7446-09-5

sulfur dioxide

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
50-150°C;
50-150°C;
sulfur dioxide
7446-09-5

sulfur dioxide

phosphorus pentafluoride
7647-19-0, 874483-74-6

phosphorus pentafluoride

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
With trifluorophosphoric acid other Radiation; CO2-laser radiation; react. rate increased by Xe or Kr, decreased by He, Ne, Ar;
pentafluorosulfanyl chloride
13780-57-9

pentafluorosulfanyl chloride

sulfur dioxide
7446-09-5

sulfur dioxide

A

sulfuryl dichloride
7791-25-5

sulfuryl dichloride

B

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

fluorosulfonyl fluoride

C

disulfur decafluoride
5714-22-7

disulfur decafluoride

D

pentafluorosulfur fluorosulfonate
81439-35-2

pentafluorosulfur fluorosulfonate

E

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: SiF4; other Radiation; photochemical reaction with 253.7 nm radiation, 48 h, in glass vessel;A n/a
B n/a
C <1
D n/a
E n/a
sulfur dioxide
7446-09-5

sulfur dioxide

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

A

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

fluorosulfonyl fluoride

B

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
Kinetics; other Radiation; no react. on mere heating at 627 °C, but induction by CO2-laser;
sulfur dioxide
7446-09-5

sulfur dioxide

tungsten(VI) fluoride
7783-82-6

tungsten(VI) fluoride

A

tungsten oxide tetrafluoride
13520-79-1, 52049-91-9

tungsten oxide tetrafluoride

B

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In liquid sulphur dioxide 20°C;
disulfur decafluoride
5714-22-7

disulfur decafluoride

sulfur dioxide
7446-09-5

sulfur dioxide

A

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

fluorosulfonyl fluoride

B

pentafluorosulfur fluorosulfonate
81439-35-2

pentafluorosulfur fluorosulfonate

C

sulfur trioxide
7446-11-9

sulfur trioxide

D

thionyl fluoride
7783-42-8

thionyl fluoride

E

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
byproducts: SiF4, sulfur; other Radiation; photochemical reaction with 253.7 nm radiation, in glass vessel;
sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

sulfur trioxide
7446-11-9

sulfur trioxide

A

fluorosulfonyl anhydride
13036-75-4

fluorosulfonyl anhydride

B

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

fluorosulfonyl fluoride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
50-150 °C, exclusion of oxygen, SO3:SF4 = 1:2;
50-150 °C, exclusion of oxygen, SO3:SF4 = 1:2;
hydrogen fluoride
7664-39-3

hydrogen fluoride

hydrogen sulfide
7783-06-4

hydrogen sulfide

A

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

fluorosulfonyl fluoride

B

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
With potassium fluoride; water In hydrogen fluoride Electrochem. Process; 5% KF, in presence of moisture, electrofluorination;
With water; sodium fluoride In hydrogen fluoride Electrochem. Process; 5% NaF, in presence of moisture, electrofluorination;
With NaF; H2O In hydrogen fluoride HF (liquid); Electrochem. Process; 5% NaF, in presence of moisture, electrofluorination;
With KF; H2O In hydrogen fluoride HF (liquid); Electrochem. Process; 5% KF, in presence of moisture, electrofluorination;
thionyl chloride
7719-09-7

thionyl chloride

zinc(II) fluoride

zinc(II) fluoride

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

sodium nitrite
7632-00-0

sodium nitrite

A

thionyl tetrafluoride
173009-97-7, 118492-84-5, 13709-54-1

thionyl tetrafluoride

B

N2O3SF5

N2O3SF5

C

thionyl fluoride
7783-42-8

thionyl fluoride

Conditions
ConditionsYield
byproducts: SF6; 200-300°C, 2-8 h;
byproducts: SF6; 200-300°C, 2-8 h;
sodium nitrate
7631-99-4

sodium nitrate

sulfur tetrafluoride
7783-60-0

sulfur tetrafluoride

A

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

fluorosulfonyl fluoride

B

thionyl tetrafluoride
173009-97-7, 118492-84-5, 13709-54-1

thionyl tetrafluoride

C

sodium fluoride

sodium fluoride

D

thionyl fluoride
7783-42-8

thionyl fluoride

E

sulphur hexafluoride
2551-62-4

sulphur hexafluoride

Conditions
ConditionsYield
byproducts: N2, NO; 200 - 300°C, 8 h; content of formed gas mixture: 27 vol.-% SOF4, 27 vol.-% SOF2, 5.2 vol.-% SF6, 1 vol.-% SO2F2, 35 vol.-% N2, 1 vol.-% NO;
byproducts: N2, NO; 200 - 300°C, 8 h; content of formed gas mixture: 27 vol.-% SOF4, 27 vol.-% SOF2, 5.2 vol.-% SF6, 1 vol.-% SO2F2, 35 vol.-% N2, 1 vol.-% NO;
chlorine monofluoride
7790-89-8

chlorine monofluoride

thionyl fluoride
7783-42-8

thionyl fluoride

pentafuorosulfanyl hypochlorite
22675-70-3

pentafuorosulfanyl hypochlorite

Conditions
ConditionsYield
cesium fluoride In neat (no solvent) absence of air and moisture; activating CsF (in stainless-steel autoclave passivated with F2) with SO2 followed by vac. pyrolysis, condensing SOF2 and excess ClF at -196°C, wrming to -40°C, standing for1 d; fractional low-temp. distn. (condensing at -120°C);99%
tetramethylammonium fluoride
373-68-2

tetramethylammonium fluoride

thionyl fluoride
7783-42-8

thionyl fluoride

tetramethylammonium trifluorosulfite

tetramethylammonium trifluorosulfite

Conditions
ConditionsYield
In neat (no solvent) Sonication; absence of air and moisture; condensing excess SOF2 onto Me4NF at -196°C, warming to room temp., placing in ultrasonic bath for few h; pumping off excess SOF2 (dry ice temp.);99%
In acetonitrile absence of air and moisture;
chlorosulfonic acid
7790-94-5

chlorosulfonic acid

aminosulfonic acid
5329-14-6

aminosulfonic acid

thionyl fluoride
7783-42-8

thionyl fluoride

bis(fluorosulfonyl)amide
14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
In 1,2-dichloro-ethane at 80℃; under 16501.7 Torr; for 17h; Solvent; Autoclave;77%

Thionyl fluoride Consensus Reports

Reported in EPA TSCA Inventory.

Thionyl fluoride 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

Thionyl fluoride Specification

The Thionyl fluoride with CAS registry number of 7783-42-8 is also known as Sulfur difluoride monoxide. The systematic name is Thionyl difluoride. Its EINECS registry number is 231-997-2. In addition, the formula is F2OS and the molecular weight is 86.06. This chemical is a colorless gas. Besides, it is a a useful reagent as the related derivative.

Physical properties about Thionyl fluoride are: (1)ACD/LogP: 0.16; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.16; (4)ACD/LogD (pH 7.4): 0.16; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)Polar Surface Area: 36.28Å2; (8)Index of Refraction: 1.376; (9)Molar Refractivity: 11.23 cm3; (10)Molar Volume: 48.9 cm3; (11)Polarizability: 4.45×10-24cm3; (12)Surface Tension: 38.7 dyne/cm; (13)Density: 1.758 g/cm3; (14)Flash Point: °C; (15)Enthalpy of Vaporization: 21.8 kJ/mol; (16)Boiling Point: °C at 760 mmHg; (17)Vapour Pressure: 7510 mmHg at 25 °C.

Preparation of  Thionyl fluoride: it is prepared by the reaction of thionyl chloride with fluoride sources such as antimony trifluoride.

3SOCl2+2SbF3→3SOF2+2SbCl3

When you are using this chemical, please be cautious about it. As a chemical, it is harmful by inhalation and may cause burns. During using it, wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell seek medical advice immediately.

You can still convert the following datas into molecular structure:
1. Canonical SMILES: O=S(F)F
2. InChI: InChI=1S/F2OS/c1-4(2)3
3. InChIKey: LSJNBGSOIVSBBR-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LCLo inhalation 260ppm/1H (260ppm) LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Archives des Maladies Professionnelles de Medecine du Travail et de Securite Sociale. Vol. 34, Pg. 581, 1973.
rabbit LCLo inhalation 1000ppm/1H (1000ppm) LUNGS, THORAX, OR RESPIRATION: ACUTE PULMONARY EDEMA

LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Archives des Maladies Professionnelles de Medecine du Travail et de Securite Sociale. Vol. 34, Pg. 581, 1973.

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