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13981-56-1

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13981-56-1 Usage

Chemical Description

Hydrogen fluoride is a colorless gas or liquid used in the production of fluorine-containing compounds.

Chemical Properties

Colorless, fuming gas or liquid. Very soluble in water. The liquid and gas consist of associated molecules. The vapor density corresponds to hydrogen fluoride only at high temperatures.Nonflammable.

Uses

Catalyst in alkylation, isomerization, condensation, dehydration, and polymerization reactions; fluorinating agent in organic and inorganic reactions; production of fluorine and aluminum fluoride; additive in liquid rocket propellants; refining of uranium

Definition

ChEBI: The radioactive isotope of fluorine with relative atomic mass 18.000938. The longest-lived fluorine radionuclide with half-life of 109.77 min.

Hazard

Toxic by ingestion and inhalation, strong irritant to eyes, skin, and mucous membranes.

Industrial uses

Hydrogen fluoride is the hydride of fluorine and the first member of the family of halogen acids. Anhydrous hydrogen fluoride is a mobile, colorless liquid that fumes strongly in air. Anhydrous hydrogen fluoride is an extremely powerful acid, exceeded in this respect only by 100% sulfuric acid. Like water, hydrogen fluoride is a liquid of high dielectric constant that undergoes self-ionization and forms conducting solutions with many solutes. Because anhydrous hydrogen fluoride is a superacid, many organic solutes dissolve in it to form stable carbonium ions. Hydrogen fluoride is a widely used industrial chemical. It was formerly used in the petroleum refining industry for the isomerization of aliphatic hydrocarbons to form more desirable automotive fuels, but this application has been superseded by other methods. The largest industrial use of hydrogen fluoride is in making fluorine- containing refrigerants (Freons, Genetrons). Another important use of hydrogen fluoride is in the preparation of organic fluorocarbon compounds by the Simons electrochemical process. In this procedure, an organic compound is dissolved in hydrogen fluoride, and an electric current is passed through the solution, whereupon the hydrogen atoms in the organic solute are replaced by fluorine. Hydrogen fluoride is employed in the electrochemical preparation of fluorine and for the preparation of inorganic fluorides. Thus, hydrogen fluoride is used for the conversion of uranium dioxide to uranium tetrafluoride, an intermediate in the preparation of uranium metal and uranium hexafluoride. With the great increase in nuclear energy-produced electricity, this represents an important use of hydrogen fluoride. Both hydrogen fluoride and hydrofluoric acid cause unusually severe burns; appropriate precautions must be taken to prevent any contact of the skin or eyes with either the liquid or the vapor.

Check Digit Verification of cas no

The CAS Registry Mumber 13981-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,8 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13981-56:
(7*1)+(6*3)+(5*9)+(4*8)+(3*1)+(2*5)+(1*6)=121
121 % 10 = 1
So 13981-56-1 is a valid CAS Registry Number.
InChI:InChI=1/FH/h1H/i1-1

13981-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name fluorine-18 atom

1.2 Other means of identification

Product number -
Other names -

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:13981-56-1 SDS

13981-56-1Synthetic route

18O-labeled water
14797-71-8

18O-labeled water

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
With proton source In water Radiochemical reaction;
Radiochemical reaction;
18F-fluoride
27948-18-1

18F-fluoride

hydrogen fluoride
7664-39-3

hydrogen fluoride

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
In neat (no solvent) at about 200°C (catalyzed by material of vessel);;
In neat (no solvent) Irradiation (UV/VIS); at room temp.;;0%
In neat (no solvent) at room temp.;;0%
(18F)-fluoride

(18F)-fluoride

tetramethylstannane
594-27-4

tetramethylstannane

A

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

B

Sn(CH3)3CH2
20670-29-5

Sn(CH3)3CH2

C

trimethylstannane radical
17272-57-0

trimethylstannane radical

Conditions
ConditionsYield
In gaseous matrix Kinetics; byproducts: CH3(18)F; other Radiation; SF6 gaseous matrix, 3000 torr, 287 +/- 2 K; content determination by radio gas chromatography;
(18F)-fluoride

(18F)-fluoride

hydrogen sulfide
7783-06-4

hydrogen sulfide

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
Kinetics; reaction of H2S with photolytically created (18)F atoms;
(18F)-fluoride

(18F)-fluoride

dimethylmercury
593-74-8

dimethylmercury

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
In gas Kinetics; byproducts: CH3Hg, CH3(18)F, CH3HgCH2; at 920-3990 Torr, also in presence CH4;
sodium hydrogendifluoride

sodium hydrogendifluoride

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
400°C;
K(1+)*H(18)F2(1-)=KH(18)F2

K(1+)*H(18)F2(1-)=KH(18)F2

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

Conditions
ConditionsYield
With HF or F2 400°C, in a nickel or copper vessel;
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

xenon difluoride
13709-36-9

xenon difluoride

[18F]xenon difluoride

[18F]xenon difluoride

Conditions
ConditionsYield
With sulfuric acid In water; acetonitrile other Radiation; by thermal neutrons irradiated (6)Li2CO3 was dissolved in H2SO4/water, H(18)F was distd. off, neutralized with n-Bu4NOH, evapd. in vac., dissolved in MeCN, evapd. in vac., dissolved in SO2ClF at -196°C, distd. into the XeF2, 20 min at 40°C; evapd. in vac. at -48°C; laser Raman spectr. at -196°C;88%
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

xenon difluoride
13709-36-9

xenon difluoride

A

XeF(18)F
331810-71-0

XeF(18)F

B

hydrogen fluoride
7664-39-3

hydrogen fluoride

Conditions
ConditionsYield
In water 0°C, 2h;A n/a
B 0.8%
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

xenon difluoride
13709-36-9

xenon difluoride

K(18)F
53612-91-2

K(18)F

A

XeF(18)F
331810-71-0

XeF(18)F

B

hydrogen fluoride
7664-39-3

hydrogen fluoride

Conditions
ConditionsYield
In water 0°C, 2h;A n/a
B 0.8%
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

potassium carbonate
584-08-7

potassium carbonate

[2.2.2]cryptande
23978-09-8

[2.2.2]cryptande

CO3(2-)*C18H36N2O6*(18)F(1-)*3K(1+)

CO3(2-)*C18H36N2O6*(18)F(1-)*3K(1+)

Conditions
ConditionsYield
In water; acetonitrile
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

potassium carbonate
584-08-7

potassium carbonate

[18F]-potassium fluoride

[18F]-potassium fluoride

[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

potassium hydroxide
1310-58-3

potassium hydroxide

[18F]-potassium fluoride

[18F]-potassium fluoride

Conditions
ConditionsYield
In [18O]-water
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

silver carbonate

silver carbonate

silver (18)fluoride

silver (18)fluoride

Conditions
ConditionsYield
In 18O-labeled water at 250℃; for 0.0833333h;
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

sodium fluoride

sodium fluoride

A

Na(18)F
22554-99-0

Na(18)F

B

hydrogen fluoride
7664-39-3

hydrogen fluoride

Conditions
ConditionsYield
complete within 3 min.;A >90
B >90
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

sodium fluoride

sodium fluoride

sodium hydrogendifluoride

sodium hydrogendifluoride

Conditions
ConditionsYield
100°C;
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

chlorine trifluoride
7790-91-2

chlorine trifluoride

A

chlorine trifluoride

chlorine trifluoride

B

hydrogen fluoride
7664-39-3

hydrogen fluoride

Conditions
ConditionsYield
In gas in 3 min;;A >90
B n/a
In neat (no solvent) in 10 min;;A >90
B n/a
In neat (no solvent) in 10 min;;A >90
B n/a
In neat (no solvent, gas phase) in 3 min;;A >90
B n/a
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

aluminium(III) chloride hexahydrate

aluminium(III) chloride hexahydrate

2,2'-(7-(2-((4-((2-(diethylamino)ethyl)carbamoyl)benzyl)amino)-2-oxoethyl)-1,4,7-triazonane-1,4-diyl)diacetic acid

2,2'-(7-(2-((4-((2-(diethylamino)ethyl)carbamoyl)benzyl)amino)-2-oxoethyl)-1,4,7-triazonane-1,4-diyl)diacetic acid

C24H36Al(18)FN6O6

C24H36Al(18)FN6O6

Conditions
ConditionsYield
Stage #1: [18F]-hydrofluoric acid; aluminium(III) chloride hexahydrate With acetic acid In aq. acetate buffer pH=4;
Stage #2: 2,2'-(7-(2-((4-((2-(diethylamino)ethyl)carbamoyl)benzyl)amino)-2-oxoethyl)-1,4,7-triazonane-1,4-diyl)diacetic acid In aq. acetate buffer at 110℃; for 0.166667h;
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

[18F]-potassium fluoride

[18F]-potassium fluoride

Conditions
ConditionsYield
With potassium carbonate; 18O-labeled water; [2.2.2]cryptande In acetonitrile
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

C15H21BF3N5O3

C15H21BF3N5O3

C15H21BF2(18)FN5O3

C15H21BF2(18)FN5O3

Conditions
ConditionsYield
In dimethyl sulfoxide pH=2 - 2.5;
[18F]-hydrofluoric acid
13981-56-1

[18F]-hydrofluoric acid

C15H22BF3N6O3*2ClH

C15H22BF3N6O3*2ClH

C15H22BF2(18)FN6O3*2ClH

C15H22BF2(18)FN6O3*2ClH

Conditions
ConditionsYield
In dimethyl sulfoxide pH=2 - 2.5;

13981-56-1Relevant articles and documents

Dodgen, H. W.,Libby, W. F.

, p. 951 - 957 (1949)

Methyl Fluoride Formation from Thermal Fluorine-18 Reaction with Dimethylmercury

McKeown, F. P.,Iyer, Subramonia R.,Rowland, F. S.

, p. 3972 - 3975 (1983)

The attack of F on (CH3)2Hg with the formation of CH3F has been observed in the gas phase by using radioactive 18F atoms thermalized by multiple collisions in SF6.Approximately 9.6 +/- 1.0percent of thermal 18F atoms are found as CH318F by the

COX-2-targeted imaging agents

-

Page/Page column 25, (2008/06/13)

The presently disclosed subject matter provides a method for synthesizing a radiological imaging agent by reacting a COX-2-selective ligand with a compound comprising a detectable group, wherein the COX-2-selective ligand is a derivative of a non-steroidal anti-inflammatory drug (NSAID) comprising an ester moiety or a secondary amide moiety. Also provided are compositions that are synthesized using the method, as well as methods of using the compositions of the presently disclosed subject matter.

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