Product Name

  • Name

    Aluminum acetylacetonate

  • EINECS 237-741-6
  • CAS No. 13963-57-0
  • Article Data12
  • CAS DataBase
  • Density 1.27 g/cm3
  • Solubility 2.5 g/L (20 °C) in water
  • Melting Point 190-193 °C(lit.)
  • Formula C15H21AlO6
  • Boiling Point 315°C(lit.)
  • Molecular Weight 324.31
  • Flash Point 314-316°C
  • Transport Information UN 3467
  • Appearance white to yellow powder or crystals
  • Safety 26-36/37/39-45-28A
  • Risk Codes 25-36/37/38-36
  • Molecular Structure Molecular Structure of 13963-57-0 (Aluminum acetylacetonate)
  • Hazard Symbols ToxicT
  • Synonyms Tris(acetylacetonate) aluminum(III);Aluminum 2,4-pentanedionate;Aluminum triacetylacetonate;Aluminum tris(acetylacetonate);CCRIS 3463;NSC 4650;
  • PSA 78.90000
  • LogP 2.88030

Synthetic route

aluminum hydroxide

aluminum hydroxide

acetylacetone
123-54-6

acetylacetone

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Conditions
ConditionsYield
at 0 - 50℃; for 0.75h;91%
acetylacetone
123-54-6

acetylacetone

AlCl3

AlCl3

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Conditions
ConditionsYield
With chloroform
With ammonia; water
acetylacetone
123-54-6

acetylacetone

Al(OH)3

Al(OH)3

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

acetyl chloride
75-36-5

acetyl chloride

AlCl3

AlCl3

A

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

B

acetylacetone
123-54-6

acetylacetone

copper bis(tetraisopropoxyaluminate)
70504-66-4, 45188-39-4

copper bis(tetraisopropoxyaluminate)

acetylacetone
123-54-6

acetylacetone

A

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

B

copper(II) acetylacetonate
13395-16-9

copper(II) acetylacetonate

Conditions
ConditionsYield
In benzene byproducts: i-propanol; the i-propoxy-complex and acetylacetone (1:8 molar ratio) were refluxedin benzene for 10 h (isopropanol was removed azeotropically out between72-80°C along with benzene); removing the solvent; elem. anal.;
aluminium trichloride
7446-70-0

aluminium trichloride

acetylacetone
123-54-6

acetylacetone

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Conditions
ConditionsYield
In water in acidic medium;
tris(o-chlorophenoxo)aluminium(III)

tris(o-chlorophenoxo)aluminium(III)

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Conditions
ConditionsYield
With acetylacetone In benzene stirring Al complex and diketone (molar ratio 1/6, slight excess) with stirring, 6h; aaddn. of petroleum ether; pptn.; recrystn. (benzene/acetone); elem. anal.;
lithium aluminium tetrahydride
16853-85-3

lithium aluminium tetrahydride

nickel(II) acetylacetonate
3264-82-2

nickel(II) acetylacetonate

A

aluminium hydride

aluminium hydride

B

nickel
7440-02-0

nickel

C

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

D

lithium pentane-2,4-dionate
18115-70-3

lithium pentane-2,4-dionate

Conditions
ConditionsYield
In tetrahydrofuran; benzene byproducts: H2; various product ratios at various reactant ratios; not isolated, detected by GLC, UV, IR;
aluminium(III) sulfate hexadecahydrate

aluminium(III) sulfate hexadecahydrate

acetylacetone
123-54-6

acetylacetone

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Conditions
ConditionsYield
Stage #1: acetylacetone With ammonia In water
Stage #2: aluminium(III) sulfate hexadecahydrate In water
C65H75N7O20

C65H75N7O20

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

2,3,9,10,16,17,23,24-tetra(15-crown-5)phthalocyaninatoaluminum(III) hydroxide

2,3,9,10,16,17,23,24-tetra(15-crown-5)phthalocyaninatoaluminum(III) hydroxide

Conditions
ConditionsYield
With 1,2,3-trichlorobenzene; phenol In octanol93%
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

tetra(15-crown-5)ed phthalocyanine
110682-72-9

tetra(15-crown-5)ed phthalocyanine

2,3,9,10,16,17,23,24-tetra(15-crown-5)phthalocyaninatoaluminum(III) hydroxide

2,3,9,10,16,17,23,24-tetra(15-crown-5)phthalocyaninatoaluminum(III) hydroxide

Conditions
ConditionsYield
With phenol In octanol; chloroform for 2h; Inert atmosphere; Reflux;93%
methanol
67-56-1

methanol

C60H45BN4O6

C60H45BN4O6

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

C62H50AlBN4O8

C62H50AlBN4O8

Conditions
ConditionsYield
In chloroform for 21h; Reflux;29%
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

A

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

B

acetone
67-64-1

acetone

Conditions
ConditionsYield
at 200 - 400℃; Pyrolysis;
fumaryl-bis-N-phenyl hydroxamic acid
87839-04-1

fumaryl-bis-N-phenyl hydroxamic acid

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Al(3+)*CH3COCHCOCH3(1-)*(CHCONOC6H5)2(2-)*3H2O=(Al(CH3COCHCOCH3)(CHCONOC6H5)2*3H2O)

Al(3+)*CH3COCHCOCH3(1-)*(CHCONOC6H5)2(2-)*3H2O=(Al(CH3COCHCOCH3)(CHCONOC6H5)2*3H2O)

Conditions
ConditionsYield
With H2O In ethanol; N,N-dimethyl-formamide mixt. of ligand and metal acetylacetonate in DMF/ethanol (1:4) is heated on a water-bath; washing with DMF/ethanol; elem. anal.;
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

fumaryl-bis-N-m-tolylhydroxamic acid

fumaryl-bis-N-m-tolylhydroxamic acid

Al(3+)*CH3COCHCOCH3(1-)*(CHCONOC6H4CH3)2(2-)*2H2O=(Al(CH3COCHCOCH3)(CHCONOC6H4CH3)2*2H2O)

Al(3+)*CH3COCHCOCH3(1-)*(CHCONOC6H4CH3)2(2-)*2H2O=(Al(CH3COCHCOCH3)(CHCONOC6H4CH3)2*2H2O)

Conditions
ConditionsYield
With H2O In ethanol; N,N-dimethyl-formamide mixt. of ligand and metal acetylacetonate in DMF/ethanol (1:4) is heated on a water-bath; washing with DMF/ethanol; elem. anal.;
phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

vanadia

vanadia

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

VO(2+)*HPO4(2-)*0.5H2O=VOHPO4*0.5H2O#dotAl

VO(2+)*HPO4(2-)*0.5H2O=VOHPO4*0.5H2O#dotAl

Conditions
ConditionsYield
With 2-methyl-propan-1-ol; water In further solvent(s) V2O5 and aluminium acetylacetonate refluxed with H3PO4 in isobutanol for16 h, filtered, washed (isobutanol/ethanol), refluxed with water for 3 h; filtration, drying in air, XRD;
yttrium(lll) nitrate hexahydrate

yttrium(lll) nitrate hexahydrate

erbium(III) nitrate pentahydrate

erbium(III) nitrate pentahydrate

Triisopropyl borate
5419-55-6

Triisopropyl borate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

yttrium erbium aluminum borate

yttrium erbium aluminum borate

Conditions
ConditionsYield
In ethanol; acetic acid; propionic acid sol-gel method; powders were mixed under N2, solvents were added, after complete dissolution at 80°C for 2-6 h water was added for hydrolysis at 80°C, 1 h, (0.9 Y:0.1 Er:3 Al:4 B:5H2O; then solvents were slow evapd. at 80°C for 14 d; resulting gels were heated at different temp. to eliminate the organic comp. and crystallize composition under O2-rich atm.; XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

(ZnO)0.30(Al2O3)070

(ZnO)0.30(Al2O3)070

Conditions
ConditionsYield
In ethanol mixing solns. of stoich. amounts of alumatrane and zinc acetate, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; powder XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

A

zinc aluminate

zinc aluminate

B

(ZnO)0.80(Al2O3)020

(ZnO)0.80(Al2O3)020

Conditions
ConditionsYield
In ethanol mixing solns. of stoich. amounts of alumatrane and zinc acetate, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; powder XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

(ZnO)0.95(Al2O3)005

(ZnO)0.95(Al2O3)005

Conditions
ConditionsYield
In ethanol mixing solns. of stoich. amounts of alumatrane and zinc acetate, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; powder XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

(ZnO)0.99(Al2O3)001

(ZnO)0.99(Al2O3)001

Conditions
ConditionsYield
In ethanol mixing solns. of stoich. amounts alumatrane and zinc acetate, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; powder XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

A

zinc aluminate

zinc aluminate

alumina

alumina

Conditions
ConditionsYield
In ethanol mixing solns. of alumatrane and zinc acetate in 9:1 molar ratio, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; quenching to room temp., powder XRD;
zinc(II) propionate
557-28-8

zinc(II) propionate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

zinc aluminate

zinc aluminate

Conditions
ConditionsYield
In ethanol mixing solns. of alumatrane and zinc acetate in 1:1 molar ratio, addn. of ethanol, stirring at room temp., aerosolizing with O2, igniting at 1500-200°C; quenching to room temp., powder XRD;
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

cobalt(II) aceylacetonate

cobalt(II) aceylacetonate

iron(III) acetylacetonate

iron(III) acetylacetonate

Co1.2Fe1.3Al1.5

Co1.2Fe1.3Al1.5

Conditions
ConditionsYield
Stage #1: aluminium acetylacetonate; cobalt(II) aceylacetonate; iron(III) acetylacetonate With hexadecane-1,2-diol; (Z)-9-octadecen-1-amine; cis-Octadecenoic acid at 100℃; Schlenk technique; Reflux;
Stage #2: at 300 - 500℃;
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

cobalt(II) aceylacetonate

cobalt(II) aceylacetonate

iron(III) acetylacetonate

iron(III) acetylacetonate

Co1.6Fe1.8Al0.6

Co1.6Fe1.8Al0.6

Conditions
ConditionsYield
Stage #1: aluminium acetylacetonate; cobalt(II) aceylacetonate; iron(III) acetylacetonate With hexadecane-1,2-diol; (Z)-9-octadecen-1-amine; cis-Octadecenoic acid at 100℃; Schlenk technique; Reflux;
Stage #2: at 300 - 700℃;
aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

cobalt(II) aceylacetonate

cobalt(II) aceylacetonate

iron(III) acetylacetonate

iron(III) acetylacetonate

Co1.4Fe1.3Al1.4

Co1.4Fe1.3Al1.4

Conditions
ConditionsYield
Stage #1: aluminium acetylacetonate; cobalt(II) aceylacetonate; iron(III) acetylacetonate With hexadecane-1,2-diol; (Z)-9-octadecen-1-amine; cis-Octadecenoic acid at 100℃; Schlenk technique; Reflux;
Stage #2: at 300 - 700℃;
iron(III)-acetylacetonate
14024-18-1

iron(III)-acetylacetonate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Fe2850Al0150O4

Fe2850Al0150O4

Conditions
ConditionsYield
In benzyl alcohol at 199.84℃; for 48h; Autoclave;
iron(III)-acetylacetonate
14024-18-1

iron(III)-acetylacetonate

aluminium acetylacetonate
13963-57-0

aluminium acetylacetonate

Al0.6Fe2.4O4

Al0.6Fe2.4O4

Conditions
ConditionsYield
In benzyl alcohol at 199.84℃; for 48h; Autoclave;

Aluminum acetylacetonate Specification

The IUPAC name of Aluminum acetylacetonate is (Z)-4-bis[[(Z)-4-oxopent-2-en-2-yl]oxy]alumanyloxypent-3-en-2-one. With the CAS registry number 13963-57-0, it is also named as Tris(acetylacetonate) aluminum(III). The product's categories are Pharmaceutical Intermediates; Organometallics; Al (Alminum) Compounds; Catalysts for Organic Synthesis; Homogeneous Catalysts; Metal Complexes; Synthetic Organic Chemistry; Classes of Metal Compounds; Typical Metal Compounds. It is white to yellow powder or crystals which is soluble in benzene, ethanol, ether and other organic solvents. In addition, it should be sealed in the container and stored in the cool and dry place.

The other characteristics of Aluminum acetylacetonate can be summarized as: (1)#H bond acceptors: 6; (2)#H bond donors: 0; (3)#Freely Rotating Bonds: 9; (4)Polar Surface Area: 78.9 Å2; (5)Rotatable Bond Count: 9; (6)Tautomer Count: 35; (7)Exact Mass: 324.115352; (8)MonoIsotopic Mass: 324.115352; (9)Topological Polar Surface Area: 78.9; (10)Heavy Atom Count: 22; (11)Complexity: 454.  

Preparation of Aluminum acetylacetonate: New distilled  acetylacetone dissolves in 40mL water. Dropping ammonia to acetyl acetone under stirring. The aluminum sulfate dissolves in water, and adding this solution to acetylacetone ammonia solution to produce precipitation. Controlling pH value is neutral during the reaction. Filtering, washing and naturally dry. Crude product is dissolved with a small amount of benzene, and filtering. Slowly dropping petroleum ether to the filtrate to produce precipitation. Filtering, washing with petroleum ether and naturally drying, then we can get the product.

Uses of Aluminum acetylacetonate: this chemical can be used as catalyst, crosslinker and glass coating. And it is also used as intermediate in organic synthesis.

When you are using this chemical, please be cautious about it as the following:
It is not only toxic if swallowed, but also irritating to eyes, respiratory system and skin. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. After contact with skin, wash immediately with plenty of soap-suds. If you want to contact this product, you must wear suitable protective clothing, gloves and eye/face protection. In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) 

People can use the following data to convert to the molecule structure. 
1. SMILES:CC(=CC(=O)C)O[Al](OC(=CC(=O)C)C)OC(=CC(=O)C)C
2. InChI:InChI=1/3C5H8O2.Al/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3

The following are the toxicity data which has been tested.

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 178mg/kg (178mg/kg)   U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02376,

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