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7616-94-6

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7616-94-6 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 7616-94-6 differently. You can refer to the following data:
1. Perchloryl fluoride is a colorless gas. Characteristic sweet odor. Shipped as a liquefied compressed gas.
2. The perchloryl fluoride,FClO3, the acyl fluoride of perchloric acid, is a stable compound. It can be prepared by electrolysis of a saturated solution of sodium perchlorate in anhydrous hydrofluoric acid.

Uses

Different sources of media describe the Uses of 7616-94-6 differently. You can refer to the following data:
1. perchloryl fluoride's uses are as an effective fluorinating agent, as an oxidant in rocket fuels, and as a gaseous dielectric for transformers.
2. In organic synthesis to introduce F atoms into organic molecules; oxidizing agent in rocket fuels; insulator for high-voltage systems
3. In organic synthesis to introduce fluorine atoms into organic molecules. As oxidizing agent; insulator for high voltage systems.

General Description

Perchloryl fluoride is a colorless, non corrosive gas with a characteristic sweet odor. Contact with the material may cause irritation to skin, eyes, and mucous membranes. Perchloryl fluoride is very toxic by inhalation and skin absorption. Under prolonged exposure to fire or intense heat the containers may violently rupture and rocket.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Perchloryl fluoride is a propellant; a powerful oxidant. Perchloryl fluoride ignites upon contact with alcohols, amines, ammonia, beryllium alkyls, boranes, dicyanogen, hydrazines, hydrocarbons, hydrogen, nitroalkanes, powdered metals, silanes, or thiols [Bretherick 1979. p.174].

Safety Profile

A poison gas which forms methemoglobin in the body and destroys red cells causing anemia, anorexia, and cyanosis. Recovery is said to be rapid, leaving no permanent physiological damage. Can be absorbed through the skin. Its odor can be detected as low as 10 ppm although this cannot be relied upon as an indication of toxic concentration in air. While nonflammable, it supports combustion. It is a powerful oxidzer. Moderately explosive. Potentially explosive reactions with combustible gases or vapors. benzene + aluminum trichloride, benzocyclobutene + butyllithium + potassium tert-butoxide, calcium acetylide, potassium cyanide, potassium thiocyanate, sodium iochde, charcoal, ethyl-4-fluorobenzoylacetate, hydrocarbons, hydrogen sulfide, nitrogen oxide, sulfur dichloride, vinylidene chloride, 3a-hydroxy-5p-androstane-1 1,17-di0ne-l 7hydrazone, lithiated compounds, 2lithio (dimet hy laminomethyl)f erroxene, methyl-2-bromo-5,5-ethylene dioxy(2,2,1)bicycloheptane-7-carboxylate, aliphatic heterocyclic amines, sodium methoxide + methanol, vinylidene chloride. Reacts to form explosive products with nitrogenous bases (e.g., isopropylamine, isobutylamine, aniline, phenyl hydrazine, 1,2-diphenyl hydrazine), sawdust, lampblack. Violent reaction with finely dwided organic materials. A fluorinating agent in chemical synthesis, and an oxidant in rocket fuel. When heated to decomposition it emits toxic fumes of Fand Cl-. See also FLUORINE and PERCHLORATES

Potential Exposure

Perchloryl fluoride has been used as a liquid oxidant in rocket propellant combinations; as an insulating gas in high voltage electrical systems; as a fluorinating agent in organic synthesis.

Shipping

UN3083 Perchloryl fluoride, Hazard Class: 2.3; Labels: 2.3-Poisonous gas, 5.1-Oxidizer, Inhalation Hazard Zone B. UN3157 Liquefied gas, oxidizing, n.o.s., Hazard Class: 2.2; Labels: 2.2-Non-flammable compressed gas, 5.1-Oxidizer, Technical Name Required. Cylinders must be transported in a secure upright position, in a well-ventilated truck. Protect cylinder and labels from physical damage. The owner of the compressed gas cylinder is the only entity allowed by federal law (49CFR) to transport and refill them. It is a violation of transportation regulations to refill compressed gas cylinders without the express written permission of the owner.

Incompatibilities

A strong oxidizing gas. Violent reaction with benzene, calcium hydride; combustibles, olefins, strong bases; sulfur, sulfuric acid; amines, reducing agents; alcohols. Contact with carbonaceous materials (such as charcoal) or finely divided metals (such as powdered magnesium and aluminum, zinc) are a fire and explosion hazard. Attacks some plastics, rubber, and coatings

Waste Disposal

Return refillable compressed gas cylinders to supplier. Incineration together with flammable solvent in furnace equipped with afterburner and scrubber.

Check Digit Verification of cas no

The CAS Registry Mumber 7616-94-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,1 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7616-94:
(6*7)+(5*6)+(4*1)+(3*6)+(2*9)+(1*4)=116
116 % 10 = 6
So 7616-94-6 is a valid CAS Registry Number.
InChI:InChI=1/ClFO3/c2-1(3,4)5

7616-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name perchloryl fluoride

1.2 Other means of identification

Product number -
Other names EINECS 231-526-0

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:7616-94-6 SDS

7616-94-6Synthetic route

potassium perchlorate

potassium perchlorate

antimony pentafluoride
7783-70-2

antimony pentafluoride

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) heating at 105°C;;97%
In neat (no solvent) heating at 105°C;;97%
potassium chlorate
3811-04-9

potassium chlorate

fluorine
7782-41-4

fluorine

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) below -20°C;; passing ClO3F over KI; cooling at -183°C; distillation at -183 - 130°C in vacuum;;60%
In neat (no solvent) below -20°C;; passing ClO3F over KI; cooling at -183°C; distillation at -183 - 130°C in vacuum;;60%
potassium chlorate
3811-04-9

potassium chlorate

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

dichlorine hexaoxide

dichlorine hexaoxide

C

chlorine dioxide
10049-04-4, 25052-55-5

chlorine dioxide

D

chlorine monofluoride
7790-89-8

chlorine monofluoride

E

chlorine
7782-50-5

chlorine

Conditions
ConditionsYield
In neat (no solvent) byproducts: O2; transport reaction: passing F2-N2 mixture over KClO3 at 25 - 60°C;; washing with NaOH; passing ClO3F through Na2S2O3 soln.; drying over NaOH and P2O5;;A 45%
B n/a
C n/a
D n/a
E n/a
perchloric acid
7601-90-3

perchloric acid

antimony pentafluoride
7783-70-2

antimony pentafluoride

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In water reaction of 60 - 62% aq. HClO4 with SbF5 at 90 - 100°C;;36%
In water reaction of 60 - 62% aq. HClO4 with SbF5 at 90 - 100°C;;36%
In neat (no solvent) reaction of 1 mol perchlorate and 3 - 10 mol SbF5 at 100 - 120°C; cooling down;; washing with Na2S2O3; condenstion at temp. of liquid air;;36-53
perchloric acid
7601-90-3

perchloric acid

fluorine
7782-41-4

fluorine

A

difluoroether
7783-41-7

difluoroether

B

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In water
dichlorine hexaoxide

dichlorine hexaoxide

fluorine
7782-41-4

fluorine

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) at 20 - 40°C;;0%
In neat (no solvent) at 20 - 40°C;;0%
hydrogen fluoride
7664-39-3

hydrogen fluoride

sodium perchlorate

sodium perchlorate

A

difluoroether
7783-41-7

difluoroether

B

perchloryl fluoride
7616-94-6

perchloryl fluoride

C

hydrogen
1333-74-0

hydrogen

D

oxygen
80937-33-3

oxygen

E

chlorine
7782-50-5

chlorine

Conditions
ConditionsYield
In neat (no solvent) Electrolysis; electrolysis of NaClO4 soln. in HF at 0 - 30°C;; condensation with liquid air; washing with Na2S2O3 soln.;;
In neat (no solvent) Electrolysis; electrolysis of NaClO4 soln. in HF at 0 - 30°C;; condensation with liquid air; washing with Na2S2O3 soln.;;
sodium perchlorate

sodium perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
Carbonyl fluoride
353-50-4

Carbonyl fluoride

lithium perchlorate

lithium perchlorate

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
With cesium fluoride byproducts: CO2, Cl2; A mixture of LiClO4 and CsF (as HF getter) was treated in a stainless steel cylinder with COF2; heating up to 120°C;0%
lithium perchlorate

lithium perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
chlorine trifluoride
7790-91-2

chlorine trifluoride

uranium(VI) trioxide

uranium(VI) trioxide

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

uranium hexafluoride
7783-81-5

uranium hexafluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
chlorine trifluoride
7790-91-2

chlorine trifluoride

uranium oxide

uranium oxide

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

uranium hexafluoride
7783-81-5

uranium hexafluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
chlorine trifluoride
7790-91-2

chlorine trifluoride

uranium dioxide

uranium dioxide

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

uranium hexafluoride
7783-81-5

uranium hexafluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
boron trifluoride
7637-07-2

boron trifluoride

potassium perchlorate

potassium perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
hydrogen fluoride
7664-39-3

hydrogen fluoride

potassium perchlorate

potassium perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
potassium perchlorate

potassium perchlorate

antimony(III) fluoride
7783-56-4

antimony(III) fluoride

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent)
In neat (no solvent)
potassium perchlorate

potassium perchlorate

antimony pentafluoride
7783-70-2

antimony pentafluoride

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) reaction of 1 mol perchlorate and 3 - 10 mol SbF5 at 100 - 120°C; cooling down;; washing with Na2S2O3; condenstion at temp. of liquid air;;36-53
potassium perchlorate

potassium perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In not given
In fluorosulphonic acid mixt. of KClO4 in fluorosulfonic acid stirred under gradual warming up to about 95°C; FClO3 was flushed with moderate N2 flow; purified through column filled with sodium thiosulfate and ascarite;
In neat (no solvent) heating KClO4 and HSO3F (10:100) at 110°C;;52-60
magnesium(II) perchlorate

magnesium(II) perchlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
In neat (no solvent) heating perchlorate with excess of HSO3F;;>80
chloryl fluoride
13637-83-7

chloryl fluoride

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
With water In water byproducts: H2;
potassium chlorate
3811-04-9

potassium chlorate

fluorosulphonic acid
7789-21-1

fluorosulphonic acid

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) heating KClO3 and 98% HSO3F at 85°C;; passing ClO3F through thiosulfate soln. and over solid KOH; condensation at temp. of liquid air;;
In neat (no solvent) heating KClO3 and 98% HSO3F at 85°C;; passing ClO3F through thiosulfate soln. and over solid KOH; condensation at temp. of liquid air;;
perchloric anhydride
12015-53-1

perchloric anhydride

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

chloryl fluoride
13637-83-7

chloryl fluoride

C

chlorine monofluoride
7790-89-8

chlorine monofluoride

D

oxygen
80937-33-3

oxygen

E

chlorine
7782-50-5

chlorine

Conditions
ConditionsYield
In neat (no solvent) Kinetics; thermal decompn. of Cl2O7 in presence of enough amounts of F2 at 100 - 120°C; reaction mechanism described;;
perchloric anhydride
12015-53-1

perchloric anhydride

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

chloryl fluoride
13637-83-7

chloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) thermal decompn. in prescence of F2;;
perchloric anhydride
12015-53-1

perchloric anhydride

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

chloryl fluoride
13637-83-7

chloryl fluoride

C

chlorine monofluoride
7790-89-8

chlorine monofluoride

Conditions
ConditionsYield
In neat (no solvent) decompn. of Cl2O7 in presence of F2 at 100 - 120°C;;
In neat (no solvent) decompn. of Cl2O7 in presence of F2 at 100 - 120°C;;
perchloric anhydride
12015-53-1

perchloric anhydride

fluorine
7782-41-4

fluorine

perchloryl fluoride
7616-94-6

perchloryl fluoride

Conditions
ConditionsYield
In neat (no solvent) formation as intermediate at 100 - 120°C;;
In neat (no solvent) formation as intermediate at 100 - 120°C;;
potassium chlorate
3811-04-9

potassium chlorate

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

dichlorine hexaoxide

dichlorine hexaoxide

Conditions
ConditionsYield
In neat (no solvent) formation of Cl2O6 as by-product;;
In neat (no solvent) formation of Cl2O6 as by-product;;
potassium chlorate
3811-04-9

potassium chlorate

fluorine
7782-41-4

fluorine

A

perchloryl fluoride
7616-94-6

perchloryl fluoride

B

chloryl fluoride
13637-83-7

chloryl fluoride

C

chlorine monofluoride
7790-89-8

chlorine monofluoride

D

chlorine
7782-50-5

chlorine

Conditions
ConditionsYield
In neat (no solvent) at -40°C;;
In neat (no solvent) at -40 or 100°C;; fractionated distillation;;
In neat (no solvent) at -40°C;;
In neat (no solvent) at -40 or 100°C;; fractionated distillation;;
perchloryl fluoride
7616-94-6

perchloryl fluoride

potassium trinitromethanide
14268-23-6

potassium trinitromethanide

fluorotrinitromethane
1840-42-2

fluorotrinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;77%
In N,N-dimethyl-formamide77%
In acetone77%
perchloryl fluoride
7616-94-6

perchloryl fluoride

trinitromethane; sodium salt

trinitromethane; sodium salt

fluorotrinitromethane
1840-42-2

fluorotrinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;77%
In N,N-dimethyl-formamide77%
In acetone77%
In methanol at 20°C 11 h;17.7%
perchloryl fluoride
7616-94-6

perchloryl fluoride

trinitromethane; ammonium salt
19836-32-9

trinitromethane; ammonium salt

fluorotrinitromethane
1840-42-2

fluorotrinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;77%
In N,N-dimethyl-formamide77%
In acetone77%
perchloryl fluoride
7616-94-6

perchloryl fluoride

<4-(Dimethylamino)phenyl>trimethylstannan

<4-(Dimethylamino)phenyl>trimethylstannan

trimethyltin fluoride

trimethyltin fluoride

Conditions
ConditionsYield
In tetrahydrofuran byproducts: dimethylphenylamine, N-(4-chloriohenyl)-N-methyl-formamide; dimethyl-(4-trimethylstannanylphenyl)amine dissolved in dry THF was cooled at -60°C; FClO3/N2 mixt. passed through soln. for about 35 min; soln. warmed up to ambient temp. under stirring and stirred at about 60°C for 20 min (closed ....; isolated by semi-preparative thin-layer chromy. (silica gel 60, petroleum ether/ethyl acetate 10:1);52%
perchloryl fluoride
7616-94-6

perchloryl fluoride

trinitromethane; lithium salt

trinitromethane; lithium salt

fluorotrinitromethane
1840-42-2

fluorotrinitromethane

Conditions
ConditionsYield
In methanol at 20°C 10 h;47%
perchloryl fluoride
7616-94-6

perchloryl fluoride

(4-methoxyphenyl)trimethylstannane
940-00-1

(4-methoxyphenyl)trimethylstannane

A

bis(4-methoxyphenyl)dimethylstannane
61726-36-1

bis(4-methoxyphenyl)dimethylstannane

B

trimethyltin fluoride

trimethyltin fluoride

Conditions
ConditionsYield
In tetrahydrofuran byproducts: methoxybenzene; (4-methoxyphenyl)trimethylstannane dissolved in dry THF was cooled at -60°C; FClO3/N2 mixt. passed through soln. for about 35 min; soln. warmed up to ambient temp. under stirring and stirred at about 60°C for 20 min (closed conditions) or; isolated by semi-preparative thin-layer chromy. (silica gel 60, petroleum ether/ethyl acetate 10:1);A n/a
B 40%
perchloryl fluoride
7616-94-6

perchloryl fluoride

A

trimethyltin fluoride

trimethyltin fluoride

B

bis-(4-(tert-butoxycarbonylamino)phenyl)dimethylstannane

bis-(4-(tert-butoxycarbonylamino)phenyl)dimethylstannane

Conditions
ConditionsYield
In tetrahydrofuran byproducts: phenylcarbamic acid tert-butyl ester; (4-trimethylstannanylphenyl)carbamic acid tert-butyl ester dissolved in dry THF was cooled at -60°C; FClO3/N2 mixt. passed through soln. for about 35 min; soln. warmed up to ambient temp. under stirring and stirred at about 60°C for 20 min; isolated by semi-preparative thin-layer chromy. (silica gel 60, petroleum ether/ethyl acetate 10:1);A 40%
B n/a
perchloryl fluoride
7616-94-6

perchloryl fluoride

Na(1+)*CBr(NO2)2(1-)=NaCBr(NO2)2
19282-10-1

Na(1+)*CBr(NO2)2(1-)=NaCBr(NO2)2

fluoro bromo dinitromethane
22632-20-8

fluoro bromo dinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;36%
In N,N-dimethyl-formamide36%
In acetone36%
perchloryl fluoride
7616-94-6

perchloryl fluoride

bromo-dinitro-methane; ammonium salt

bromo-dinitro-methane; ammonium salt

fluoro bromo dinitromethane
22632-20-8

fluoro bromo dinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;36%
In N,N-dimethyl-formamide36%
In acetone36%
perchloryl fluoride
7616-94-6

perchloryl fluoride

bromo-dinitro-methane; potassium salt
24280-12-4

bromo-dinitro-methane; potassium salt

fluoro bromo dinitromethane
22632-20-8

fluoro bromo dinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;36%
In N,N-dimethyl-formamide36%
In acetone36%
perchloryl fluoride
7616-94-6

perchloryl fluoride

Na(1+)*CCl(NO2)2(1-)=NaCCl(NO2)2
19282-07-6

Na(1+)*CCl(NO2)2(1-)=NaCCl(NO2)2

fluorochlorodinitromethane
19845-51-3

fluorochlorodinitromethane

Conditions
ConditionsYield
In further solvent(s) in CH3O(CH2)2OCH3;33%
In N,N-dimethyl-formamide33%
In acetone33%

7616-94-6Relevant articles and documents

Rohrback, G. H.,Cady, G. H.

, p. 677 - 678 (1947)

On the reaction of 4-substituted trimethyltin aromatics with perchlorylfluoride

Hiller, Achim,Patt, J?rg T.,Steinbach, J?rg

, p. 3737 - 3742 (2007/10/03)

To evaluate the suitability of [18F]perchorylfluoride [18F]FClO3 as an electrophilic fluorination agent for the preparation of radiopharmaceuticals, the reactivity non-radioactive FClO3 towards 4-substituted trimethyltin aromatic compounds was studied. Contrary to the expectation, an electrophilic fluorination of the aromatic nucleus did not occur. The reaction of perchlorylfluoride with aromatic trimethylstannyl compounds resulted in the formation of trimethyltin fluoride and the respective destannylated aromatics in variable yields.

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