Gallium acetate

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Gallium acetate
Gallium acetate.png
Names
IUPAC names
Tetra-μ2-acetatodiaquadigallium(III), diacetyloxygallanyl acetate gallium(3+) triacetate
Other names
  • Gallium ethanoate
  • Gallium triacetate
  • Gallium(III) acetate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.018.106 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 219-915-3
PubChem CID
  • InChI=1S/3C2H4O2.Ga/c3*1-2(3)4;/h3*1H3,(H,3,4);/q;;;+3/p-3
    Key: FYWVTSQYJIPZLW-UHFFFAOYSA-K
  • CC(=O)O[Ga](OC(=O)C)OC(=O)C
Properties
Ga(O2C2H3)3
Molar mass 246.85 [1]
Appearancewhite crystals
Density 1.57 g/cm/3
Melting point N/A
Boiling point 117.1C
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg
Danger
H314, H335
P261, P280, P304+P340, P305+P351+P338, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
The depiction of one of the bonding anions in gallium acetate. Acetate anion.png
The depiction of one of the bonding anions in gallium acetate.

Gallium acetate is a salt composed of a gallium atom trication and three acetate groups as anions where gallium exhibits the +3 oxidation state. It has a chemical formula of Ga(CH3COO)3 although it can be informally referred to as GaAc because Ac is an informal symbol for acetate. Gallium is moderately water-soluble and decomposes to gallium oxide when heated to around 70  °C. [2] Gallium acetate, like other acetate compounds, is a good precursor to ultra-pure compounds, catalysts and nanoscale materials. [2] Gallium acetate is being considered as a substitute in de-icing compounds like calcium chloride and magnesium chloride. [3]

Contents

Preparation

Gallium acetate can be formed using a neutralization reaction (acetic acid reacts with gallium oxide or gallium hydroxide):

6CH3COOH + Ga2O3 → 2Ga(CH3COO)3 + 3H2O
3CH3COOH + Ga(OH)3 → Ga(CH3COO)3 + 3H2O

Gallium can also be refluxed in acetic acid for several weeks to produce gallium acetate. [4]

Applications

It can also be used in conjunction with acetylacetonate bis(thiosemicarbazone) to create radiogallium-acetylacetonate bis(thiosemicarbazone) complex. It can be used in tumor imaging. [5]

See also

Related Research Articles

<span class="mw-page-title-main">Carboxylic acid</span> Organic compound containing a –C(=O)OH group

In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.

In chemistry, a salt is a chemical compound consisting of an ionic assembly of positively charged cations and negatively charged anions, which results in a compound with no net electric charge. A common example is table salt, with positively charged sodium ions and negatively charged chloride ions.

<span class="mw-page-title-main">Acetate</span> Salt compound formed from acetic acid and a base

An acetate is a salt formed by the combination of acetic acid with a base. "Acetate" also describes the conjugate base or ion typically found in aqueous solution and written with the chemical formula C
2
H
3
O
2
. The neutral molecules formed by the combination of the acetate ion and a positive ion are also commonly called "acetates". The simplest of these is hydrogen acetate with corresponding salts, esters, and the polyatomic anion CH
3
CO
2
, or CH
3
COO
.

The Brønsted–Lowry theory (also called proton theory of acids and bases) is an acid–base reaction theory which was proposed independently by Johannes Nicolaus Brønsted and Thomas Martin Lowry in 1923. The fundamental concept of this theory is that when an acid and a base react with each other, the acid forms its conjugate base, and the base forms its conjugate acid by exchange of a proton (the hydrogen cation, or H+). This theory is a generalization of the Arrhenius theory.

In organic chemistry, acetylation is an organic esterification reaction with acetic acid. It introduces an acetyl group into a chemical compound. Such compounds are termed acetate esters or simply acetates. Deacetylation is the opposite reaction, the removal of an acetyl group from a chemical compound.

<span class="mw-page-title-main">Acetic anhydride</span> Chemical compound

Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH3CO)2O. Commonly abbreviated Ac2O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with moisture in the air.

<span class="mw-page-title-main">Sodium acetate</span> Chemical compound

Sodium acetate, CH3COONa, also abbreviated NaOAc, is the sodium salt of acetic acid. This colorless deliquescent salt has a wide range of uses.

<span class="mw-page-title-main">Acetyl chloride</span> Chemical compound

Acetyl chloride (CH3COCl) is an acyl chloride derived from acetic acid. It belongs to the class of organic compounds called acid halides. It is a colorless, corrosive, volatile liquid. Its formula is commonly abbreviated to AcCl.

Aluminium acetate or aluminium ethanoate (also "aluminum ~"), sometimes abbreviated AlAc in geochemistry, can refer to a number of different salts of aluminum with acetic acid. In the solid state, three salts exist under this name: basic aluminium monoacetate, (HO)2AlCH3CO2, basic aluminium diacetate, HOAl(CH3CO2)2, and neutral aluminium triacetate, Al(CH3CO2)3. In aqueous solution, aluminium triacetate hydrolyses to form a mixture of the other two, and all solutions of all three can be referred to as "aluminium acetate" as the species formed co-exist and inter-convert in chemical equilibrium.

<span class="mw-page-title-main">Potassium acetate</span> Chemical compound

Potassium acetate (CH3COOK) is the potassium salt of acetic acid. It is a hygroscopic solid at room temperature.

<span class="mw-page-title-main">Acetic acid</span> Colorless and faint organic acid found in vinegar

Acetic acid, systematically named ethanoic acid, is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH. Vinegar is at least 4% acetic acid by volume, making acetic acid the main component of vinegar apart from water and other trace elements.

<span class="mw-page-title-main">Magnesium acetate</span> Chemical compound

Anhydrous magnesium acetate has the chemical formula Mg(C2H3O2)2 and in its hydrated form, magnesium acetate tetrahydrate, it has the chemical formula Mg(CH3COO)2 • 4H2O. In this compound magnesium has an oxidation state of 2+. Magnesium acetate is the magnesium salt of acetic acid. It is deliquescent and upon heating, it decomposes to form magnesium oxide. Magnesium acetate is commonly used as a source of magnesium in biological reactions.

<span class="mw-page-title-main">Barium acetate</span> Chemical compound

Barium acetate (Ba(C2H3O2)2) is the salt of barium(II) and acetic acid. Barium acetate is toxic to humans, but has use in chemistry and manufacturing.

Aluminium triacetate, formally named aluminium acetate, is a chemical compound with composition Al(CH
3
CO
2
)
3
. Under standard conditions it appears as a white, water-soluble solid that decomposes on heating at around 200 °C. The triacetate hydrolyses to a mixture of basic hydroxide / acetate salts, and multiple species co-exist in chemical equilibrium, particularly in aqueous solutions of the acetate ion; the name aluminium acetate is commonly used for this mixed system.

<span class="mw-page-title-main">Aluminium monoacetate</span> Chemical compound

Aluminium monoacetate, also known as dibasic aluminium acetate, and formally named dihydroxy aluminium acetate, is a salt of aluminium with acetic acid. It has the formula Al(OH)2(CH3COO), with aluminium in an oxidation state of +3, and appears under standard conditions as a white solid powder.

<span class="mw-page-title-main">Neodymium acetate</span> Compound of neodymium

Neodymium acetate is an inorganic salt composed of a neodymium atom trication and three acetate groups as anions where neodymium exhibits the +3 oxidation state. It has a chemical formula of Nd(CH3COO)3 although it can be informally referred to as NdAc because Ac is an informal symbol for acetate. It commonly occurs as a light purple powder.

<span class="mw-page-title-main">Praseodymium(III) acetate</span> Compound of praseodymium

Praseodymium(III) acetate is an inorganic salt composed of a Praseodymium atom trication and three acetate groups as anions. This compound commonly forms the dihydrate, Pr(O2C2H3)3·2H2O.

<span class="mw-page-title-main">Europium(III) acetate</span> Chemical compound

Europium(III) acetate is an inorganic salt of europium and acetic acid with the chemical formula of Eu(CH3COO)3. In this compound, europium exhibits the +3 oxidation state. It can exist in the anhydrous form, sesquihydrate and tetrahydrate. Its hydrate molecule is a dimer.

<span class="mw-page-title-main">Lutetium(III) acetate</span> Compound of lutetium

Lutetium(III) acetate is the acetate salt of lutetium with the chemical formula of Lu(CH3COO)3.

<span class="mw-page-title-main">Holmium acetate</span> Compound of holmium

Holmium acetate is the acetate salt of holmium, with a chemical formula of Ho(CH3COO)3.

References

  1. "Gallium acetate".
  2. 1 2 Elements, American. "Gallium Acetate". American Elements. Retrieved 2022-05-05.
  3. "Gallium acetate, 99.9% 2571-06-4 - Manufacturers & Suppliers in India with worldwide shipping". www.ottokemi.com. Retrieved 2022-05-05.
  4. Funk, H.; Paul, A. Chemistry of gallium. II. Reactions between gallium and organic compounds. Zeitschrift für Anorganische und Allgemeine Chemie (1965), 337(3-4), 142-4.
  5. Jalilian, Amir R.; Yousefnia, Hassan; Garousi, Javad; Novinrouz, Aytak; Rajamand, Amir A.; Shafaee, Kamaledin (2009). "The development of radiogallium-acetylacetonate bis(thiosemicarbazone) complex for tumour imaging". Nuclear Medicine Review. 12 (2): 65–71. ISSN   1644-4345.