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139-12-8

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139-12-8 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 139-12-8 differently. You can refer to the following data:
1. Aluminum acetate, AL(C2H302)3,is white crystals, soluble, by reaction of aluminum hydroxide and acetic acid and then crystallizing. Used as a mordant in dyeing and printing textiles, in the manufacturing of lakes, for fire proofing fabrics, for waterproofing cloth.
2. CH3COONH4 is hygroscopic and decomposes easily to acetamide if heated above 165 °C. CH3COONH4 → CH3C(O)NH2 + H2O In this reaction, a salt is converted to two molecular species, which is a relatively uncommon conversion at mild temperatures.
3. white powder(s); preparation: by heating aluminum or AlCl3 with an acetic acid solution containing acetic anhydride; uses: as an antiseptic, an astringent, and in antiperspirant applications; there is a hydroxyaluminum diacetate, CAS RN 142-03-0 [CIC73] [HAW93] [ALD94]

Description

Different sources of media describe the Description of 139-12-8 differently. You can refer to the following data:
1. Aluminum acetate is a chemical compound and is a salt which can be produced by the reaction of aluminum hydroxide and acetic acid. The compound formula for Aluminum Acetate is Al(CH3COO)3.
2. Ammonium acetate is a chemical compound with the formula NH4C2H3O2 (or C2H4O2.NH3 or C2H7NO2). It is a white solid and can be derived from the reaction of ammonia and acetic acid. It is available commercially and, depending on grade, can be rather inexpensive.

Uses

Astringent.

Definition

Different sources of media describe the Definition of 139-12-8 differently. You can refer to the following data:
1. A salt obtained by reaction of aluminum hydroxide and acetic acid with subsequent recrystallization. Its neutral form Al(C 2 H 3 O 2 ) 3 is a white, water-soluble powder used in solution as an antiseptic, astringent, and antiperspirant. Its basic form is Al(C 2 H 3 O 2 ) 2 OH, also known as aluminum diacetate and aluminum subacetate. It is a crystalline solid, insoluble in water, used as a mordant in textile dyeing, as a flame retardant and waterproofing agent, and in manufacture of lakes and pigments.
2. (aluminum acetate; Al(OOCCH3)3) A white solid soluble in water. It is usually obtained as the dibasic salt, basic aluminum ethanoate, Al(OH)(CH3COO)2. It is prepared by dissolving aluminum hydroxide in ethanoic acid and is used extensively as a mordant in dyeing and as a size for paper and cardboard products. The solution is hydrolyzed and contains various complex aluminumhydroxyl species and colloidal aluminum hydroxide.

Application

The diacetate is used as an antiseptic. The Aluminum Acetate compound can be used medicinally to treat infections in the outer ear canal. It is used in the name brand drug Domeboro, which contains acetic acid/aluminum acetate.This medication kills the infectious bacteria and fungus as well as drying out the ear canal. Since it acts as a drying agent, it can also be used in the treatment of severe rashes, such as poison ivy, poison oak, and poison sumac.

Production Methods

Ammonium acetate is produced by the neutralization of acetic acid with ammonium carbonate or by saturating glacial acetic acid with dry ammonia gas. Obtaining crystalline ammonium acetate is difficult on account of its aqueous solution giving off ammonia when evaporated.

Brand name

Buro-Sol Concentrate (Doak); Domeboro (Bayer).

Industrial uses

As the salt of a weak acid and a weak base, ammonium acetate has a number of distinctive properties. NH4C2H3O2 is occasionally employed as a biodegradable deicing agent. It is often used with acetic acid to create a buffer solution, one that can be thermally decomposed to non-ionic products Ammonium acetate is useful as a catalyst in the Knoevenagel condensation and as a source of ammonia in the Borch reaction in organic synthesis. It is a relatively unusual example of a salt that melts at low temperatures.Can be used with distilled water to make a protein precipitating reagent. Is often used as an aqueous buffer for ESI mass spectrometry of proteins and other molecules. Ammonium acetate is volatile at low pressures. Because of this it has been used to replace cell buffers with non-volatile salts, in preparing samples for mass spectrometry.It is also popular as a buffer for mobile phases for HPLC with ELSD detection for this reason. Other volatile salts that have been used for this include ammonium formate.

Synthesis

The triacetate forms when aluminum sulfate is mixed with barium acetate. Another synthetic method is by bringing together aluminum hydroxide, acetic anhydride and glacial acetic acid in water, forming the basic aluminum monoacetate The diacetate is prepared in a reaction of sodium aluminate (NaAlO2) with acetic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 139-12-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139-12:
(5*1)+(4*3)+(3*9)+(2*1)+(1*2)=48
48 % 10 = 8
So 139-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H4O2.Al/c1-2(3)4;/h1H3,(H,3,4);/q;+3/p-1

139-12-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Aluminum acetate

1.2 Other means of identification

Product number -
Other names Aluminiumacetaetbasic

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:139-12-8 SDS

139-12-8Synthetic route

acetic anhydride
108-24-7

acetic anhydride

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With aluminium trichloride Abdestillieren des gebildeten Acetylchlorids und Erhitzen des Rueckstands auf 160-180grad;
acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With aluminium trichloride
acetic anhydride
108-24-7

acetic anhydride

Al(O+C2H5)3

Al(O+C2H5)3

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
at 90℃;
((CH3)2CHO)Al(OCOCH3)2

((CH3)2CHO)Al(OCOCH3)2

A

aluminum acetate
139-12-8

aluminum acetate

B

aluminum isopropoxide
555-31-7

aluminum isopropoxide

Conditions
ConditionsYield
In neat (no solvent) symmetrization on heating;;
sodium aluminium sulfate dodecahydrate

sodium aluminium sulfate dodecahydrate

lead acetate
301-04-2

lead acetate

A

Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

B

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water purification from Pb ions with H2S, from SO4 ions with barium acetate;
In water purification from Pb ions with H2S, from SO4 ions with barium acetate;
aluminum tri-tert-butoxide
556-91-2

aluminum tri-tert-butoxide

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With diethylsulfide In benzene byproducts: (C2H5)2SO2; addn. of t-BuOOH to soln. of (t-BuO)3Al and Et2S in benzene for 1-2 min at 20°C; condencing of solvent and volatile components with liq. N2; addn. of H2SO4 to residue, treatment with acetic acid; filtration, removal of volatiles under reduced pressure;
With diisopropylsulfide In benzene byproducts: (isopropyl)2SO2; addn. of t-BuOOH to soln. of (t-BuO)3Al and i-Pr2S in benzene for 1-2 min at 20°C; condencing of solvent and volatile components with liq. N2; addn. of H2SO4 to residue, treatment with acetic acid; filtration, removal of volatiles under reduced pressure;
With dimethylsulfide In benzene byproducts: (CH3)2SO2; addn. of t-BuOOH to soln. of (t-BuO)3Al and Me2S in benzene for 1-2 min at 20°C; condencing of solvent and volatile components with liq. N2; addn. of H2SO4 to residue, treatment with acetic acid; filtration, removal of volatiles under reduced pressure;
aluminum tri-tert-butoxide
556-91-2

aluminum tri-tert-butoxide

acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With tert.-butylhydroperoxide In benzene byproducts: (isopropyl)2SO2, (CH3)3COH; (Ar); addn. of (CH3)3COOH (2 equiv.) to soln. of ((CH3)3CO)3Al (1 equiv.) and (isopropyl)2S (1 equiv.) in benzene at 20°C; self-heating; treatment with AcOH; filtration; removal of volatiles under reduced pressure;
With tert.-butylhydroperoxide; diethyl sulphide In benzene byproducts: (C2H5)2SO2, (CH3)3COH; (Ar); addn. of (CH3)3COOH (2 equiv.) to soln. of ((CH3)3CO)3Al (1 equiv.) and (C2H5)2S (1 equiv.) in benzene at 20°C; self-heating; treatment with AcOH; filtration; removal of volatiles under reduced pressure;
With tert.-butylhydroperoxide; dimethylsulfide In benzene byproducts: (CH3)2SO2, (CH3)3COH; (Ar); addn. of (CH3)3COOH (2 equiv.) to soln. of ((CH3)3CO)3Al (1 equiv.) and (CH3)2S (1 equiv.) in benzene at 20°C; self-heating; treatment with AcOH; filtration; removal of volatiles under reduced pressure;
acetic acid
64-19-7

acetic acid

aluminium
7429-90-5

aluminium

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water Electrochem. Process; electrolytical dissolution of Al in acetic acid; calcium acetate addition for increase of electric conductivity;
dissolving Al in water free acetic acid;
In water influence of concentration and temperature were examined;
aluminium trichloride
7446-70-0

aluminium trichloride

acetic acid
64-19-7

acetic acid

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
water free AlCl3, water free acetic acid; driving away HCl; inpurity less then 1 % Cl;
aluminum(III) sulfate

aluminum(III) sulfate

acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With barium carbonate In water
With calcium carbonate In water
With BaCO3 In water
With CaCO3 In water
aluminum trihydroxide

aluminum trihydroxide

acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water
In water
With acetic anhydride In acetic acid Al(OH)3 in 1:1-mixt. of glacial acetic acid and acetic anhydride refluxed for 24 h; suspn. filtered, solid washed with acetone;
ammonium aluminium sulfate

ammonium aluminium sulfate

acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
With hydroxide In acetic acid Al(OH)3 pptd. from soln. of aluminum ammonium sulfate; Al(OH)3 filtered out; quickly dissolved in glacial CH3COOH;
aluminum(III) sulfate

aluminum(III) sulfate

barium(II) acetate
543-80-6

barium(II) acetate

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water equiv. amount of educts;
In water equiv. amount of educts;
aluminium trichloride
7446-70-0

aluminium trichloride

silver(I) acetate
563-63-3

silver(I) acetate

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water
In water
aluminium trichloride
7446-70-0

aluminium trichloride

acetic anhydride
108-24-7

acetic anhydride

A

aluminum acetate
139-12-8

aluminum acetate

B

acetyl chloride
75-36-5

acetyl chloride

Conditions
ConditionsYield
distn. the formed acetyl chloride and heating the residue at 160-180 °C;
distn. the formed acetyl chloride and heating the residue at 160-180 °C;
aluminum(III) sulfate

aluminum(III) sulfate

lead acetate
301-04-2

lead acetate

A

Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

B

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water purification from Pb ions with H2S, from SO4 ions with barium acetate;
In water purification from Pb ions with H2S, from SO4 ions with barium acetate;
aluminum(III) sulfate

aluminum(III) sulfate

calcium acetate
62-54-4

calcium acetate

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
In water
In water
aluminum ethoxide
555-75-9

aluminum ethoxide

acetic anhydride
108-24-7

acetic anhydride

A

aluminum acetate
139-12-8

aluminum acetate

B

ethyl acetate
141-78-6

ethyl acetate

Conditions
ConditionsYield
heating at 90 °C and distn. the formed ethyl acetate;
heating at 90 °C and distn. the formed ethyl acetate;
Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

Al(3+)*OH(1-)*2CH3C(O)O(1-) = (CH3C(O)O)2AlOH

acetic anhydride
108-24-7

acetic anhydride

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
heating in sealed tube;
heating in sealed tube;
((CH3)3CO)Al(OCOCH3)2

((CH3)3CO)Al(OCOCH3)2

A

aluminum acetate
139-12-8

aluminum acetate

B

aluminum tri-tert-butoxide
556-91-2

aluminum tri-tert-butoxide

Conditions
ConditionsYield
In neat (no solvent) symmetrization on heating;;
Allyl acetate
591-87-7

Allyl acetate

phenylaluminium dichloride
3530-39-0

phenylaluminium dichloride

A

allylbenzene
300-57-2

allylbenzene

B

biphenyl
92-52-4

biphenyl

C

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
tetrakis(triphenylphosphine) palladium(0) In diethyl ether Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 20 h);A 0%
B <1
C n/a
aluminum (III) chloride
7446-70-0, 7784-13-6

aluminum (III) chloride

acetic anhydride
108-24-7

acetic anhydride

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
Stage #1: acetic anhydride With acetic acid at 110℃; for 0.5h;
Stage #2: aluminum (III) chloride at 20℃;
aluminum (III) chloride
7446-70-0, 7784-13-6

aluminum (III) chloride

acetic acid
64-19-7

acetic acid

aluminum acetate
139-12-8

aluminum acetate

Conditions
ConditionsYield
at 100℃; for 0.166667h;
aluminum acetate
139-12-8

aluminum acetate

baicalin
21967-41-9

baicalin

C42H34AlO22

C42H34AlO22

Conditions
ConditionsYield
In aq. acetate buffer at 50℃; for 1h; pH=5; pH-value; Temperature;94.38%
octakis(benzylthio)phthalocyaninato lithium

octakis(benzylthio)phthalocyaninato lithium

aluminum acetate
139-12-8

aluminum acetate

octakis(benzylthio)phthalocyaninato aluminium

octakis(benzylthio)phthalocyaninato aluminium

Conditions
ConditionsYield
In pentan-1-ol mixt. of octakis(benzylthio)phthalocyaninato lithium and metal salt wererefluxed in n-pentanol for 1 h, cooled to room temp.; centrifuged, washed with hot EtOH, dried in desiccator;69%
thionyl chloride
7719-09-7

thionyl chloride

aluminum acetate
139-12-8

aluminum acetate

acetic anhydride
108-24-7

acetic anhydride

aluminum acetate
139-12-8

aluminum acetate

chlorine
7782-50-5

chlorine

sulfur

sulfur

acetic anhydride
108-24-7

acetic anhydride

aluminum acetate
139-12-8

aluminum acetate

A

carbon dioxide
124-38-9

carbon dioxide

B

acetic acid
64-19-7

acetic acid

C

acetone
67-64-1

acetone

Conditions
ConditionsYield
at 320℃;
aluminum acetate
139-12-8

aluminum acetate

acetic acid
64-19-7

acetic acid

hydrogen

hydrogen

aluminium hydroxide

aluminium hydroxide

Conditions
ConditionsYield
at 320 - 360℃;
zinc diacetate
557-34-6

zinc diacetate

aluminum acetate
139-12-8

aluminum acetate

zinc aluminate

zinc aluminate

Conditions
ConditionsYield
Stage #1: zinc diacetate; aluminum acetate With potassium hydroxide In water at 20℃; pH=14; Acidic conditions;
Stage #2: With acetic acid In water pH=8;
cupric chloride

cupric chloride

aluminum acetate
139-12-8

aluminum acetate

1,2-diacetoxypropane
623-84-7

1,2-diacetoxypropane

Conditions
ConditionsYield
With acetic anhydride In acetic acid
sulfur dioxide
7446-09-5

sulfur dioxide

aluminum acetate
139-12-8

aluminum acetate

aluminium sulfite

aluminium sulfite

Conditions
ConditionsYield
slow reaction, 90°C;
slow reaction, 90°C;
Al2O3(b),Na2O(0.04),O2Si(0.053),Fe2O3(0.006) (W%)

Al2O3(b),Na2O(0.04),O2Si(0.053),Fe2O3(0.006) (W%)

aluminum acetate
139-12-8

aluminum acetate

corundum

corundum

Conditions
ConditionsYield
With ammonium fluoride; manganese(II) acetate In water to anodic aluminum hydroxyde added satd. solns. of ammonium fluoride, aluminum acetate, and manganese acetate; mixt. heated at 1000-1200°C for 0.5-5 h; elem. anal.;
aluminum acetate
139-12-8

aluminum acetate

alumina

alumina

mullite

mullite

Conditions
ConditionsYield
Al salt introduced into SiO2 sol, hydrolyzed, pptd. by (CH2)6N4, heatedat 1200-1250°C for 1 h; not isolated, detected by XRD;
Na2O*3WO3*4H2O

Na2O*3WO3*4H2O

aluminum acetate
139-12-8

aluminum acetate

aluminium polytungstate

aluminium polytungstate

Conditions
ConditionsYield
In water pptn. and washing with ethanol;
sodium oxalate
62-76-0

sodium oxalate

aluminum acetate
139-12-8

aluminum acetate

A

sodium aluminate

sodium aluminate

aluminium oxide

aluminium oxide

Conditions
ConditionsYield
In neat (no solvent) mixt. heated at 950°C for 1 h, mixt. ground up in a mortar, fired at 900°C for 1 h in air; not isolated, mixt. of phases: NaAlO2 and γ-Al2O3;
sodium oxalate
62-76-0

sodium oxalate

aluminum acetate
139-12-8

aluminum acetate

A

sodium aluminate

sodium aluminate

aluminium oxide

aluminium oxide

alumina

alumina

Conditions
ConditionsYield
In neat (no solvent) mixt. heated at 950°C for 10 h, mixt. ground up in a mortar, fired at 900°C for 1 h in air; not isolated, mixt. of phases: NaAlO2, β-Al2O3 and γ-Al2O3;

139-12-8Relevant articles and documents

Acid-Mediated Synthesis of Ordered Mesoporous Aluminosilicates: The Challenge and the Promise

Krishna, Nunna V.,Selvam, Parasuraman

, p. 1604 - 1612 (2017)

A new intrinsic hydrolysis method was employed, for the first-time, to synthesize well-ordered H-AlSBA-15 with trivalent aluminium exclusively in the tetrahedral framework structure of SBA-15. Unlike other methods, which involve incorporation of aluminium ions in both the framework (Br?nsted) and non-framework (Lewis) sites of the silicate matrix, the intrinsic hydrolysis method isomorphously substitutes aluminium ions in the tetrahedral network even at high aluminium content. This unique approach relies mainly on the hydrolysis rates of the inorganic (silicon and aluminium) precursors used for the preparation in such a way that the condensation occurs simultaneously so as to overcome the usually encountered difficulties in stabilizing aluminium ions in the silicate matrix. In this way, we could successfully synthesize high quality Br?nsted acidic H-AlSBA-15, hitherto not reported. The synthesized materials were systematically characterized by various analytical, spectroscopic, and imaging techniques, including XRD, Brunauer–Emmett–Teller (BET) surface area measurements, TEM, SEM,29Si and27Al magic angle spinning NMR spectroscopy, X-ray fluorescence (XRF), and NH3temperature-programmed desorption (TPD). The characterization results reveal the presence of a highly porous structure (with narrow pores) and tetrahedrally coordinated trivalent aluminium in the silicate matrix with more medium to strong Br?nsted acid sites. The resulting high quality catalysts exhibit excellent activity for tert-butylation of phenol with high selectivity towards para-tert-butyl phenol and 2,4-di-tert-butyl phenol.

Bi-inorganic-ligand coordinated colloidal quantum dot ink

Jiang, Xianyuan,Li, Hansheng,Shang, Yuequn,Wang, Fei,Chen, Hao,Xu, Kaimin,Yin, Ming,Liu, Hefei,Zhou, Wenjia,Ning, Zhijun

, p. 9483 - 9486 (2019)

Quantum dot light emitting diodes (QLEDs) are rising as a promising light emitting technology. However, the widely used insulating organic ligands hamper carrier injection. Herein, we developed a bi-inorganic-ligand strategy to replace organic ligands and dispersed QDs in a benign solvent butylamine. The all-inorganic QD film shows enhanced luminescence intensity and superior thermal stability and conductivity. In the end, we exploited the first prototype all inorganic QLED.

Oxygen activation on metallic centers and oxidizing abilities of such oxygen

Zaburdaeva, Elena A.,Dodonov, Viktor A.,Stepovik, Larisa P.

, p. 1265 - 1268 (2007)

It was shown that metallcontaining peroxides such as XOOOBu-t [X = (t-BuO)2Al, (t-BuO)3Ti] generate molecular oxygen in the electron-excited singlet state (1O2). These ozonides and η2-peroxocomplex Ph3Bi(η2O2) demonstrate high oxidative activity towards some classes of organic substances under mild conditions (20 °C).

Crum, W.

, p. 216 (1854)

Liquid-phase oxidation of sulfides by an aluminum (and titanium) tert-butoxide - tert-butyl hydroperoxide system

Dodonov,Zaburdaeva,Stepovik

, p. 1729 - 1734 (2007/10/03)

A system aluminum (and titanium) tert-butoxide-tert-butyl hydroperoxide (1 : 2) under mild conditions (20°C, 1 h) oxidizes aliphatic and alkylaromatic sulfides and diphenyl sulfide to the corresponding sulfones in yields close to ~100%. The oxidation is induced by electron-excited dioxygen formed upon thermal decomposition of intermediate metal-containing peroxy trioxides (ozonides). The latter are formed as a result of the reversible reaction of aluminum or titanium tert-butoxides with tert-butyl hydroperoxide followed by the interaction of di-tert-butoxy-tert-butylperoxyaluminum and tri-tert-butoxy-tert-butylperoxytitanium that formed with another Bu tOOH molecule. Alkminum-containing peroxide (ButO) 2AlOOBut oxidizes sulfides to sulfoxides.

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