Aluminium bromide supplier | CasNO.7727-15-3

Name
Aluminum bromide
EINECS 231-779-7
CAS No. 7727-15-3
Article Data70
CAS DataBase
Density 3.205 g/mL at 25 °C(lit.)
Solubility decomposes in water
Melting Point 94-98 °C(lit.)
Formula AlBr₃
Boiling Point 265 °C
Molecular Weight 266.694
Flash Point 268°C subl.
Transport Information UN 3264 8/PG 2
Appearance white crystalline powder
Safety 9-16-26-29-36/37/39-43-45-60-61-62-28-27
Risk Codes 23/24/25-34-22-14-67-65-50/53-11
Molecular Structure
Hazard Symbols C,Xi,N,F
Synonyms Aluminumbromide (8CI);Aluminum tribromide;Aluminum tribromide (AlBr3);NSC 87608;Aluminum bromide(AlBr3);
PSA 0.00000
LogP 2.53680

Synthetic route

: 3530-39-0
phenylaluminium dichloride

: 106-95-6
allyl bromide

A: 300-57-2
allylbenzene

B: 92-52-4
biphenyl

C: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
bis(η3-allyl-μ-chloropalladium(II)) In diethyl ether Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 8 h);	A 94% B <1 C n/a
tetrakis(triphenylphosphine) palladium(0) In diethyl ether Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 20 h);	A <1 B <1 C n/a

...Expand

: 6591-30-6
diphenylaluminum chloride

: 106-95-6
allyl bromide

A: 300-57-2
allylbenzene

B: 92-52-4
biphenyl

C: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
tetrakis(triphenylphosphine) palladium(0) In diethyl ether Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 20 h);	A 37% B <1 C n/a

...Expand

: 74-95-3
1,1-dibromomethane

aluminium: aluminium

A: 74-85-1
ethene

B: 7727-15-3
aluminium bromide

...Expand

: 75-25-2
Bromoform

aluminium: aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
Erhitzen des Reaktionsprodukts im Vakuum auf 200grad;

: 1333-84-2, 1344-28-1
aluminum oxide

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
With bromine; pyrographite In not given heating;
With bromine; pyrographite heating;
With sulfur dibromide In solid 350°C, with vaporous sulfur bromide;

: 1333-84-2, 1344-28-1
aluminum oxide

: 13172-31-1
disulphur dibromide

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
reaction started at 350°C and accelerated by raising of temp.; excess of S2Br2 removed with HBr or nitrogen;
reaction started at 350°C and accelerated by raising of temp.; excess of S2Br2 removed with HBr or nitrogen;

: 7726-95-6
bromine

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
With aluminum(III) sulfate In water heating on water bath with small amt. of Br2 and H2O;
With bisilicates; carbon heating;
With carbon; silicates heating;

: 7784-27-2
aluminium trinitrate

: 7726-95-6
bromine

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In not given heating on water bath with small amt. of Br2;
In not given heating on water bath with small amt. of Br2;

: 7726-95-6
bromine

: 7429-90-5
aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In gas Al and Br2 in vac. were vaporized separately and reacted in gaseous state; distd. in vac.;
With air; water in moist air containing Br2 condensation of droplets of a soln. of AlBr3 occurs on a gray layer that has formed first;;
In neat (no solvent) start of react. by heating;;

: 7429-90-5
aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
With bromine reacted in the presence of AlBr3;
With bromine Al heated in combustion tube; with H2 or N2 deluted Br2 lead over Al;
With bromine Al sheet heated in combustion tube; vaporous Br2 leaded over Al; AlBr3 flowed out from tube;

: 106-93-4
ethylene dibromide

: 7429-90-5
aluminium

A: 74-85-1
ethene

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In ethylene dibromide
In ethylene dibromide

...Expand

: 7789-67-5
stannic bromide

: 7429-90-5
aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In not given heating of Al with SnBr4 for 30 min gives AlBr3;;

: tin(II) bromide

: 7429-90-5
aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In neat (no solvent) reaction with SnBr2 under formation of AlBr3 above 216°C;; differentialthermoanalytic examinations;;

: 7429-90-5
aluminium

: mercury dibromide

A: mercury(I) bromide

B: 7727-15-3
aluminium bromide

C: mercury

Conditions

Conditions	Yield
at higher temp.;;

...Expand

: AlBr3*Br4*CS2

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
byproducts: Br2, CS2; decompn. at 150°C;
byproducts: Br2, CS2; decompn. at 150°C;

: 2AlBr3*Br4*CS2

A: CS2Br4

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
at 200°C;
at 200°C;

: 506-68-3
bromocyane

: 7429-90-5
aluminium

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
120°C;
120°C;

: zinc(II) selenide

: AlSeBr

A: Zn2AlSe3Br

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In neat (no solvent) mixt. of the starting materials heated in evacuated sealed quartz tubes to 500-900°C; decompn. of educts ocurrs, AlBr3 sublimates off;	A 0% B n/a

...Expand

: 7789-60-8
phosphorus tribromide

: 7429-90-5
aluminium

: phosphorous

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In neat (no solvent) reaction at 100°C;;
In neat (no solvent) reaction at 100°C;;

...Expand

: 10097-32-2
bromine

: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
With sulfur introducing a vapor of a soln. of S in Br2 over Al oxide;
With S introducing a vapor of a soln. of S in Br2 over Al oxide;

: 119484-32-1
AsBr4(1+)*AlBr4(1-)={AsBr4}{AlBr4}

A: 7726-95-6
bromine

B: 7727-15-3
aluminium bromide

C: 7784-33-0
arsenic(III) bromide

Conditions

Conditions	Yield
equilibrium at room temp.;

...Expand

: lithium{aluminum-bromo(μ-dibromo)-tetrakis(tert-butoxy)titanate}

A: titanium(IV) tetrabutoxide

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
With copper(l) chloride In tetrahydrofuran byproducts: Cu, LiCl; to a soln. of Ti-complex in THF at 0°C is added CuCl; pptn. of Cu, solvent is removed in vac., the residue is dissolved in toluene, pptd. LiCl is centrifuged off, the soln. is vacuum-evaporated, from the residue at 90-110°C is distilled the complex, crystn. at 20°C, elem. anal.;

: {(CO)3Fe(P(C6H5)3)2Br}(1+)*AlBr4(1-)={(CO)3Fe(P(C6H5)3)2Br}AlBr4

A: 14741-34-5, 21255-52-7
tricarbonyl bis(triphenylphosphine) iron

B: 51744-69-5, 15020-31-2, 84622-99-1
bis(triphenylphosphine)dicarbonyldibromoiron(II)

C: 7726-95-6
bromine

D: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In tetrahydrofuran	A <1 B n/a C n/a D n/a
In methanol	A <1 B n/a C n/a D n/a
In dichloromethane	A <1 B n/a C n/a D n/a

...Expand

: 361447-05-4
tetraiodophosphonium tetrabromoaluminate

A: 7727-15-3
aluminium bromide

B: 7789-33-5
iodine(I) bromide

C: 13455-01-1
phosphorous triiodide

Conditions

Conditions	Yield
In carbon disulfide under N2, anaerobic and anhyd. conditions; dissolved in CS2;

...Expand

: dibromo[3-(dimethylamino)propyl]aluminium

A: 22359-97-3
aluminium(I) bromide

B: 136684-48-5
AlBr2

C: 74-90-8, 6914-07-4
hydrogen isocyanide

D: 7727-15-3
aluminium bromide

E: dibromoaluminium hydride

Conditions

Conditions	Yield
In neat (no solvent, gas phase); solid matrix byproducts: CH4, H2C=CH2, H2C=CHCH3; N2 atmosphere, high vacuum (1E-6 to 1E-7 mbar) thermolysis at 1000°C, trapping in argon at 15 K; further organic byproducts: H2C=N(CH3)2 and H2CCHCH2; IR-monitoring;

...Expand

: aluminum bromide fluoride

: 7784-18-1
aluminium(III) fluoride

B: 7727-15-3
aluminium bromide

Conditions

Conditions	Yield
In solid heating at 400°C;

: 16853-85-3
lithium aluminium tetrahydride

: 124-11-8
non-1-ene

: 7727-15-3
aluminium bromide

: 180334-67-2
1-dibromoaluminiononane

Conditions

Conditions	Yield
In diethyl ether; benzene Ar, LiAlH4 in ether added to benzene under stirring, most of the solvent removed, benzene and AlBr3 in benzene added, stirred at 20°C for 1 h, org. compound in benzene added dropwise under stirring, warmed to30-40°C for 5-10 min; NMR;	100%

...Expand

: 7727-15-3
aluminium bromide

: 920-36-5, 90269-51-5
(2-methylpropyl)lithium

: magnesium bromide

: magnesium tetra(isobutyl)aluminate

Conditions

Conditions	Yield
In hexane; toluene byproducts: LiBr; to stirred mixt. of MgBr2, AlBr3 and toluene at room temp., soln. of iso-C4H9Li in hexane added (Ar; ratio MgBr2, AlBr3, RLi: 1:2:8) within 20 min; react. for 3.0 h at 80°C; ppt. filtered off (Ar); (1)H NMR of soln.;	100%

...Expand

: 7727-15-3
aluminium bromide

: 108-98-5
thiophenol

: 98772-99-7
aluminium tribromide*ethanethiol

Conditions

Conditions	Yield
In benzene under N2, dropwise addn. of thiol soln. to a suspension of AlBr3 in benzene, dissoln. of AlBr3, stirred for 15 min at room temp.; evapn. of solvent, dried in vac. at room temp. for 3h, elem. anal.;	100%

: 2432-11-3
(1,1';3',1''-terphenyl)-2'-ol

: 7727-15-3
aluminium bromide

: aluminium tris(2,6-diphenylphenoxide)

Conditions

Conditions	Yield
With tetraallyltin In benzene byproducts: SnBr4, propene; 2,6-diphenylphenol (12 equiv.) treated with AlBr3 (4 equiv.) in benzene at room temp., tetraallyltin (3 equiv.) added, stirred at room temp. for1 h, solvent evapd. in vacuo for 3 h with concomitant removal of SnBr4 and propene;	100%

: 74-93-1
methylthiol

: 7727-15-3
aluminium bromide

: 98772-98-6
aluminium tribromide*methanethiol

Conditions

Conditions	Yield
In benzene under N2, CH3SH introduced in a suspension of AlBr3 for 7 min, dissoln.of AlBr3, stirred for 15 min at room temp.; evapn. of solvent, dried in vac. at room temp. for 3h, elem. anal.;	100%

: 3908-55-2
Trimethyl(methylthio)silane

: 7727-15-3
aluminium bromide

: 112908-14-2
aluminium tribromide*trimethylsilyl methyl sulphide

Conditions

Conditions	Yield
In benzene a benzene soln. of Me3SiSMe was added dropwise under N2 to a suspn. of AlBr3 in benzene, mixt. was stirred for 15 min at room temp.; solvent was evapd.; elem. anal.;	100%

: 5573-62-6
(ethylthio)trimethylsilane

: 7727-15-3
aluminium bromide

: 112908-15-3
aluminium tribromide*trimethylsilyl ethyl sulphide

Conditions

Conditions	Yield
In benzene a benzene soln. of Me3SiSEt was added dropwise under N2 to a suspn. of AlBr3 in benzene, mixt. was stirred for 15 min at room temp.; solvent was evapd.; elem. anal.;	100%

: 4551-15-9
phenylthiotrimethylsilane

: 7727-15-3
aluminium bromide

: 112908-16-4
aluminium tribromide*trimethylsilyl phenyl sulphide

Conditions

Conditions	Yield
In benzene a benzene soln. of Me3SiSPh was added dropwise under N2 to a suspn. of AlBr3 in benzene, mixt. was stirred for 15 min at room temp.; solvent was evapd.; elem. anal.;	100%

disupersilyl aluminum bromide: disupersilyl aluminum bromide

: 7727-15-3
aluminium bromide

: 374569-92-3
supersilylaluminum dibromide

Conditions

Conditions	Yield
In n-heptane Kinetics; all manipulations with exclusion of air and moisture; compd. prepd. fromAlBr3 and org. compd. reacted in molar ratio of 1:1 at room temp. for 2 4 d (yield depended on react. time); controlled by NMR; volatiles evapd. by oil pump, residue dissolved in heptane, NaBr filtered;	100%

: 7789-65-3
selenium tetrabromide

: 7727-15-3
aluminium bromide

: 69951-93-5
tribromoselenium(IV) tetrabromoaluminate

Conditions

Conditions	Yield
In neat (no solvent) Ar atm. (300 mbar); heating (150-200°C, several days);	100%
In dichloromethane addn. of AlBr3 to SeBr4, stirring (2 h); filtration (under dry N2), drying (vac.); elem. anal.;

: (S)-3,3-bis(3,5-dimethylphenyl)-1-(2,4,6-trifluorophenyl)tetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole

: 7727-15-3
aluminium bromide

: (S)-3,3-bis(3,5-dimethylphenyl)-1-(2,4,6-trifluorophenyl)tetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborol-7-ium-7-yltribromoaluminate

Conditions

Conditions	Yield
In dichloromethane; ethylene dibromide	100%

: (S)-3,3-bis(2,3-dimethylphenyl)-1-(2,4,6-trifluorophenyl)tetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole

: 7727-15-3
aluminium bromide

: C27H27AlBBr3F3NO

Conditions

Conditions	Yield
In dichloromethane; ethylene dibromide	100%

: WH2(η-cyclopentadienyl)2

: 7727-15-3
aluminium bromide

: 79560-37-5
bis(η5-cyclopentadienyl)tungsten dihydride * AlBr3

Conditions

Conditions	Yield
In diethyl ether stoich. amts. (pptn.);	99%

: 55664-33-0
bis(tricyclohexylphosphine)platinum(0)

: 7727-15-3
aluminium bromide

: 960294-94-4
[(Cy3P)2Pt(AlBr3)]

Conditions

Conditions	Yield
In benzene AlBr3 was added to a soln. of Pt-complex in benzene, the soln. was kept at room temp. for 24 h;	99%
In toluene (Ar); Al salt added to a soln. of Pt complex; evapd. (vac.); elem. anal.;	98%

: thallium(I) bromide

: 7727-15-3
aluminium bromide

: 114064-41-4
Tl(1+)*AlBr4(1-)=TlAlBr4

Conditions

Conditions	Yield
In neat (no solvent, solid phase) (Ar); solid state reaction; equimolar mixt. of TlBr, and AlBr3 sealed under vac. in glass ampoules; heated with 10°C/h to 150°C for 48 h; cooled to 25°C with 2.degre.C/h; detn. by XRD;	99%

: 110-71-4
1,2-dimethoxyethane

: 7727-15-3
aluminium bromide

: 182561-85-9
aluminium tribromide-1,2-dimethoxyethane

Conditions

Conditions	Yield
In toluene (N2); stirring (1 h); filtration, washing (toluene); elem. anal.;	98.7%

: 7727-15-3
aluminium bromide

: 53201-03-9
sodium triethoxysilanolate

A: tris(triethoxysiloxy)aluminum

B: 7647-15-6
sodium bromide

Conditions

Conditions	Yield
In benzene (glovebox); addn. of a soln. of AlBr3 in C6H6 to a soln. of silicon compd. in C6H6 in vac. with stirring, sealing, heating to 40°C for 30min with shaking; centrifugation, decantation, evapn; elem. anal.;	A 98% B 98%

...Expand

: 176763-62-5
(1R,2R)-(-)-N,N'-bis(3,5-di-tert-butylsalicydene)-1,2-cyclohexanediaminocobalt(II)

: 7727-15-3
aluminium bromide

: [AlBr3(Co((R,R)-C6H10(NCHC6H2O(tert-butyl)2)2))]

Conditions

Conditions	Yield
In dichloromethane; water addn. of Co(C6H10(NCHC6H2O(t-Bu)2)2) (1 equiv.) to soln. of AlBr3 (1 equiv.) in CH2Cl2/H2O; stirring at room temp. for 1 h; concn. under reduced pressure, treatment with H2O and CH2Cl2;	98%

: [(S,S)-Carbox-iPr]H

: 7727-15-3
aluminium bromide

: (S,S)-1,7-bis(1-bromo-3-methylbutanamide-2-yl)-1,7-dicarba-closo-dodecaborane

Conditions

Conditions	Yield
With I2 In dichloromethane a mixt. of B compd., I2, and AlBr3 in CH2Cl2 refluxed for 16.5 h under N2; poured into ice-cold H2O, the org. phase sepd., the aq. layer extd. (Et2O), the combined org. phase washed (Na2S2O3 soln., then H2O), dried (MgSO4), solvent-removed, recrystd. (hexane); elem. anal.;	98%

: 109-99-9
tetrahydrofuran

: 97355-16-3
N,N-bis(2-hydroxy-3,5-di-tert-butylphenyl)amine

: 7727-15-3
aluminium bromide

: 1384526-06-0
[bis(3,5-di-tert-butyl-2-phenol)amine(2-)]AlBr(THF)

Conditions

Conditions	Yield
With KH In tetrahydrofuran under inert atm. mixt. ligand and KH in THF were stirred at room temp. for 2 h, soln. was frozen, AlBr3 was added upon thawing, stirred at room temp. overnight; solvent was removed in vacuo, residue was co-evapd. with pentane; elem. anal.;	98%

...Expand

: 503-17-3
dimethylacetylene

: 7727-15-3
aluminium bromide

: 70492-15-8
C4(CH3)4*AlBr3

Conditions

Conditions	Yield
In methyl cyclohexane addn. of 2-butyne to soln. of AlBr3, 0°C, stirred 15h at 25°C, filtered, washed with methylcyclohexane, dried in vac.; elem. anal.;	97%

: 15226-74-1, 61091-28-9, 61117-58-6
dicobalt octacarbonyl

: 7727-15-3
aluminium bromide

: Co2(CO)8*AlBr3

Conditions

Conditions	Yield
In n-heptane room temp.;	97%
In benzene room temp.;	97%
In benzene room temp.;	97%

: 7727-15-3
aluminium bromide

: 653-38-3
(pentafluoro phenyl) methyl mercury

: 4457-90-3
(pentafluoro phenyl) dibromo alane

Conditions

Conditions	Yield
In neat (no solvent) heating of the components ( molar ratio 1 : 1) in a closed tube at 70°C, 5 days;;	97%

: uranium dioxide

: 7727-15-3
aluminium bromide

: 13470-20-7
uranium(IV) bromide

Conditions

Conditions	Yield
Stage #1: uranium dioxide; aluminium bromide at 250℃; for 12h; Sealed tube; Stage #2: at 350℃; for 144h; Sealed tube;	97%

: 16853-85-3
lithium aluminium tetrahydride

: 79-92-5
camphene

: 7727-15-3
aluminium bromide

: C10H17AlBr2

Conditions

Conditions	Yield
In diethyl ether; benzene Ar, LiAlH4 in ether added to benzene under stirring, most of the solvent removed, benzene and AlBr3 in benzene added, stirred at 20°C for 1 h, org. compound in benzene added drowise under stirring, warmed to 30-40°C for 5-10 min; NMR;	96%

...Expand

: 26944-84-3
1,3-dimethyl-2-dimethylaminodiazaborolane

: 7727-15-3
aluminium bromide

: 1,3-dimethyl-2-(dimethylamino)-1,3,2-diazaborolidine-1,3-bis(aluminum-tribromide)

Conditions

Conditions	Yield
under N2, at -78°C; excess of Lewis-acid used; elem. anal.;	96%

: 122-99-6
2-Phenoxyethanol

: 7727-15-3
aluminium bromide

: 223647-11-8
[(μ-2-phenoxyethanolate)AlBr2]2

Conditions

Conditions	Yield
In toluene N2-atmosphere; slow addn. of Al-salt to slight excess of alcohol at 25°C, stirring for 4 h; drying (vac.), extn. into CH2Cl2, drying (vac.); elem. anal.;	96%

: 168292-74-8
potassium triethoxysilanolate

: 7727-15-3
aluminium bromide

A: potassium tetrakis(triethoxysiloxy)aluminates

B: 7558-02-3
potassium bromide

Conditions

Conditions	Yield
In benzene (glovebox); dropwise addn. of a soln. of AlBr3 in C6H6 to a soln. of silicon compd. in C6H6 over 15 min with stirring, refluxing for 7 h; centrifugation, decantation, evapn.; elem. anal.;	A 88% B 96%

...Expand

: 211381-77-0
(2,2,6,6-tetramethylpiperidino)2AlBr(isoquinoline)

: 7727-15-3
aluminium bromide

: 211381-88-3
(2,2,6,6-tetramethylpiperidino)2Al(isoquinoline) tetrabromoaluminate

Conditions

Conditions	Yield
In Bromoform inert atmosphere, addn. of soln. of AlBr3 to soln of isoquinoline complex at 0°C, 30 min; reduction of volume, crystn. (-20°C, overnight); elem. anal.;	96%

: 16853-85-3
lithium aluminium tetrahydride

: 625-65-0
2,4-dimethyl-2-pentene

: 7727-15-3
aluminium bromide

: 180334-71-8
(CH3)2CHCH(AlBr2)CH(CH3)CH3

Conditions

Conditions	Yield
In diethyl ether; benzene Ar, LiAlH4 in ether added to benzene under stirring, most of the solvent removed, benzene and AlBr3 in benzene added, stirred at 20°C for 1 h, org. compound in benzene added drowise under stirring, warmed to 30-40°C for 5-10 min; NMR;	96%

...Expand

Aluminium bromide Chemical Properties

IUPAC Name: Tribromoalumane
Molecular Formula: AlBr₃
Formula Weight: 266.69g/mol
EINECS: 231-779-7
Melting Point: 94-98 °C(lit.)
Boiling Point: 265 °C
Density: 3.205 g/mL at 25 °C(lit.)
Vapor Pressure: 1 mm Hg ( 81.3 °C)
Flash Point: 268°C subl.
Chemical Properties: White crystalline powder
Water Solubility: Decomposes
Sensitive: Moisture sensitive
Stability: Stable, but reacts violently with water. Incompatible with aqueous solutions, alcohols, acids.
Synonyms of Aluminium bromide (7727-15-3): Aluminum bromide ; Aluminum bromide Hexahydrate ; Aluminium tribromide ; AlBr3 ; Aluminum bromide (AlBr3); Aluminum bromide , anhydrous ; Aluminumbromide (albr3)
Product Categories of Aluminium bromide (7727-15-3): Inorganics ; Aluminum salts ; Aluminummetal and ceramic science ; Aluminumsynthetic reagents ; Catalysis and inorganic chemistry ; Chemical synthesis ; Crystal grade inorganics ; Lewis acids ; Salts
Structure of Aluminium bromide (7727-15-3):

Aluminium bromide Safety Profile

Safety Statements: 9-16-26-29-36/37/39-43-45
9: Keep container in a well-ventilated place
16: Keep away from sources of ignition - No smoking
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
29: Do not empty into drains
36/37/39: Wear suitable protective clothing, gloves and eye/face protection
43: In case of fire, use ... (indicate in the space the precise type of fire-fighting equipment. If water increases the risk add - Never use water)
45: In case of accident or if you feel unwell, seek medical advice immediately (show label where possible)
WGK Germany: 3
Hazard Note: Irritant
Hazard Class: 8
Risk Statements: 23/24/25-34-22-14-67-65-50/53-11
23/24/25: Toxic by inhalation, in contact with skin and if swallowed
34: Causes burns
22: Harmful if swallowed
14: Reacts violently with water
67: Vapors may cause drowsiness and dizziness
65: Harmful: May cause lung damage if swallowed
50/53: Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
11: Highly Flammable

Aluminium bromide Specification

General Description: A white to yellowish-red lumpy solid with a pungent odor.

Product Name

Aluminum bromide

Synthetic route

Aluminium bromide Chemical Properties

Aluminium bromide Safety Profile

Aluminium bromide Specification

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