Zinc acetate supplier | CasNO.557-34-6

Name
Zinc acetate
EINECS 209-170-2
CAS No. 557-34-6
Article Data82
CAS DataBase
Density 1.84
Solubility Soluble in water, alcohol, dilute mineral acids and alkalies.
Melting Point 83-86 °C
Formula C₄H₆O₄Zn
Boiling Point 117.1 °C at 760 mmHg
Molecular Weight 631.827
Flash Point 40 °C
Transport Information
Appearance white crystalline powder
Safety 26-60-61-39-16-7
Risk Codes 36-50/53-22-11
Molecular Structure
Hazard Symbols Xn,N,Xi,F
Synonyms Acetic acid, zincsalt (8CI,9CI);Zinc acetate (6CI,7CI);Galzin;Siltex CL 4;Zinc diacetate;Zinc(II) acetate;
PSA 37.30000
LogP 0.08840

Synthetic route

: 591-87-7
Allyl acetate

: 28557-00-8
phenylzinc chloride

A: 300-57-2
allylbenzene

B: 92-52-4
biphenyl

C: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran Ar atmosphere; stirring (20°C, 5 mole-% catalyst, 5 h);	A 100% B 0% C n/a

...Expand

: 557-20-0
diethylzinc

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With acetic acid In diethyl ether N2 atmosphere; dropwise addn. of CH3COOH in Et2O to soln. of ZnEt2 (molar ratio Zn/acid 1:2), pptn.; filtration off, washing (Et2O), drying (vac.);	99%

: 6-bromopyridine-2-carbaldehyde oxime

: 64-19-7
acetic acid

: 7440-66-6
zinc

A: 6-(bromopyridin-2-yl)methanammonium acetate

B: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
at 20℃; for 0.166667h; Inert atmosphere;	A 95% B 82 mg

...Expand

: 127-09-3
sodium acetate

: 7440-66-6
zinc

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In acetic acid Electrolysis; on electrolysis of Na acetate in acetic acid at 280V, 7mA/cmxcm, formation of acetate at Zn anode;;	85%
In acetic acid Electrolysis; on electrolysis of Na acetate in acetic acid at 280V, 7mA/cmxcm, formation of acetate at Zn anode;;	85%

: 79-41-4
poly(methacrylic acid)

: 64-19-7
acetic acid

: 743369-26-8
zinc(II) carbonate

A: 557-34-6
zinc diacetate

B: 272771-37-6
zinc methacryliate acetate

Conditions

Conditions	Yield
In water at 20℃; for 2h;	A n/a B 43%

...Expand

: 108-24-7
acetic anhydride

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With zinc hydroxide
With zinc(II) nitrate

: 64-19-7
acetic acid

A: 557-34-6
zinc diacetate

B: 75-07-0
acetaldehyde

C hydrogen: hydrogen

Conditions

Conditions	Yield
at 250 - 280℃; Ueberleiten ueber Zinkstaub;

...Expand

: 75-15-0
carbon disulfide

: 938-81-8
N-nitrosoacetanilide

zinc: zinc

: 557-34-6
zinc diacetate

...Expand

: 64-19-7
acetic acid

dehydrated Zn(C2H3O2)2: dehydrated Zn(C2H3O2)2

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
at 150℃;

: 108-24-7
acetic anhydride

dihydrate Zn(C2H3O2)2+2 H2O: dihydrate Zn(C2H3O2)2+2 H2O

: 557-34-6
zinc diacetate

Zn(C2H3O2)2+2 H2O: Zn(C2H3O2)2+2 H2O

: 557-34-6
zinc diacetate

: 67-56-1
methanol

: 557-34-6
acetic acid ; tetrazinc-hexaacetate oxide

A: 557-34-6
zinc diacetate

B zinc oxide: zinc oxide

...Expand

: 64-17-5
ethanol

: 557-34-6
acetic acid ; tetrazinc-hexaacetate oxide

A: 557-34-6
zinc diacetate

B zinc oxide: zinc oxide

...Expand

: 7732-18-5
water

: 557-34-6
acetic acid ; tetrazinc-hexaacetate oxide

A: 557-34-6
zinc diacetate

B zinc oxide: zinc oxide

...Expand

: 584-08-7
potassium carbonate

: 7646-85-7
zinc(II) chloride

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With acetic acid In water

: 64-19-7
acetic acid

: 743369-26-8
zinc(II) carbonate

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In not given prepn. from ZnCO3 and carboxylic acid in molar ratio 1:2;
In not given neutralizing acetic acid with the carbonate; slow evapn.;
In water at 100℃; for 3h;

: 5970-45-6
zinc(II) acetate dihydrate

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With chloroform byproducts: H2O; on dehydration of dihydrate with chloroform;;
In neat (no solvent) byproducts: H2O; loss of 2 mole H2O at 100 °C;;
In neat (no solvent) byproducts: H2O; vac. dehydration at 363 K, according to: G. Maslowska, A. Baranowska, Prod. Eighth Conf. Coord. Chem., Smolenice, Bratislava, 1980, pp. 269-273;

: 5970-45-6
zinc(II) acetate dihydrate

: 108-24-7
acetic anhydride

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In neat (no solvent) on react. of acetic anhydride with Zn acetate dihydrate at 10°C for a period of 27 hours;;
In neat (no solvent) on react. of acetic anhydride with Zn acetate dihydrate at 10°C for a period of 27 hours;;

: nitrosoacetanilide

: 7440-66-6
zinc

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In carbon disulfide byproducts: N2; decompn. of nitrosoacetanilide with Zn dust and forming of Zn acetate and N2;;

: zinc(II) oxide

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With acetic acid In hydrogenchloride; water; acetic acid ZnO dissoln. in solvents mixt.; evapn. to dryness (hot plate, 90°C), further drying (vac. desiccator, 4 h); X-ray diffraction;
With acetic acid In water; acetic acid ZnO dissoln. in solvents mixt.; concn. (hot plate, 90°C), air-cooling to room temp. (28+/-2°C), crystn. for 24 h, filtn., washing (ethyl alcohol), drying (vac. desiccator, 2 h); X-ray diffraction;

: 142-71-2
copper diacetate

: zinc sulfide

A: 557-34-6
zinc diacetate

B: copper(II) sulfide

Conditions

Conditions	Yield
In water shaken for 24 h at 25.0°C; evapn. of filtrate to dryness;

...Expand

: 64-19-7
acetic acid

: 7440-66-6
zinc

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In acetic acid on slow heating of Zn with glacial acetic acid;;

: 100-52-7
benzaldehyde

: 64-19-7
acetic acid

: 7440-66-6
zinc

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In acetic acid byproducts: C6H5CH2OCOCH3; addn. of mixt. of benzaldehyde and excess acetic acid to zinc dust, stirring ( room temp., 12 h); filtration;

...Expand

: basic zinc acetate

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With H2O In neat (no solvent, solid phase) byproducts: Zn(OH)2; decompn. in solid state (moisture); IR-spectroscopy;

: zinc(II) acetate * 0.5 acetic acid

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
With acetic acid on treating with acetic acid;;
With acetic acid
With acetic acid
With acetic acid on treating with acetic acid;;

: 108-24-7
acetic anhydride

: zinc(II) hydroxide

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In neat (no solvent) on react. of acetic anhydride with Zn(OH)2 at 138°C for a period of 4 hours;;
at 138°C, some acetate is formed;;
at 138°C, some acetate is formed;;
In neat (no solvent) on react. of acetic anhydride with Zn(OH)2 at 138°C for a period of 4 hours;;

: 301-04-2
lead acetate

: 7440-66-6
zinc

A: 7439-92-1
lead

B: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In water in 0.1n soln.;;	A n/a B >99

...Expand

: zinc(II) nitrate hexahydrate

: 127-09-3
sodium acetate

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
In water Kinetics; dissolving both components in distilled water; stoichiometric concentrations: Zn 0.1 - 0.8 M, acetate 0.1 - 0.4 M; pH of solution from 4 to 6;; ultrasonic absorptions spectra;;

: 124-38-9
carbon dioxide

: 544-97-8
dimethyl zinc(II)

: 557-34-6
zinc diacetate

Conditions

Conditions	Yield
2,6-bis[(di-t-butylphosphino)methyl]phenyl palladium trifluoroacetate In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at room temp.;
Pd(methyl)((1,3-bis[(di-tert-butylphosphino)methyl]benzene)(-1H)) In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at 100°C;
Pd(acetyl)((1,3-bis[(di-tert-butylphosphino)methyl]benzene)(-1H)) In benzene CO2 was reacted with ZnMe2 in C6H6 in presence of Pd catalyst at 100°C;

: 557-34-6
zinc diacetate

: 54604-95-4, 54649-48-8
(22S)-22-Hydroxy-6β-methoxy-3α,5α-cyclocholest-24-ene

A: 54604-97-6, 64938-06-3, 114718-53-5
(22S)-3β-Acetoxy-22-hydroxycholesta-5,24-diene

B: 54604-96-5, 64938-05-2
Acetic acid (S)-1-[(S)-1-((3S,10R,13S)-3-acetoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-ethyl]-4-methyl-pent-3-enyl ester

Conditions

Conditions	Yield
In acetic acid for 1h; Heating;	A 100% B n/a

...Expand

: 557-34-6
zinc diacetate

: TPP-=-Ph-CHO

: 4-(trans-2'-(2''-(5'',10'',15'',20''-tetraphenylporphyrinato zinc(II)yl)ethen-1'-yl))-1-benzaldehyde

Conditions

Conditions	Yield
In methanol; chloroform at 20℃; for 0.333333h;	100%

: 557-34-6
zinc diacetate

: 5,12-Bis-(3,5-di-tert-butyl-phenoxy)-2-(2-ethyl-hexyl)-9-[4-((5Z,10Z,15Z,19Z)-10,15,20-tri-p-tolyl-14,21,23,24-tetrahydro-porphin-5-yl)-phenyl]-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone

: C107H98N6O6(2-)*Zn(2+)

Conditions

Conditions	Yield
In methanol; chloroform for 0.25h; Heating;	100%

: 557-34-6
zinc diacetate

: C182H178N8O13

: C182H174N8O13(2-)*Zn(2+)

Conditions

Conditions	Yield
In methanol; chloroform for 1h; Heating;	100%

: 5,15-bis([2',2'':5'',2'''-terthiophen]-3''-yl)-2,8,12,18-tetra-n-butyl-3,7,13,17-tetramethylporphyrin

: 557-34-6
zinc diacetate

: 5,15-bis([2',2'':5'',2'''-terthiophen]-3''-yl)-2,8,12,18-tetra-n-butyl-3,7,13,17-tetramethylporphyrinato zinc(II)

Conditions

Conditions	Yield
In methanol; chloroform; water at 20℃; for 0.5h;	100%

: TPP-=-CHO

: 557-34-6
zinc diacetate

: 3-[(E)-4-(3-oxoprop-1-en-1-yl)]-5,10,15,20 tetraphenylporphyrinatozinc(II)

Conditions

Conditions	Yield
In methanol; chloroform at 20℃; for 0.166667h;	100%

: 1,9-bis[(propylimino)methyl]-5-phenyldipyrromethane

: 557-34-6
zinc diacetate

: 2C23H26N4(2-)*2Zn(2+)

Conditions

Conditions	Yield
In ethanol at 20℃; for 0.166667h; Product distribution / selectivity;	100%

: 553-26-4
4,4'-bipyridine

: 557-34-6
zinc diacetate

: 110-17-8
(2E)-but-2-enedioic acid

: [Zn2(fumarate)2(4,4'-bipyridyl)]n

Conditions

Conditions	Yield
	100%

...Expand

: 126956-54-5
C20H6N4(CH3)4(C2H5)2(C2H4COOC3H6C6H4N(CH3)2)(C2H4COOC2H4SC10H4O2(CH3))

: 557-34-6
zinc diacetate

: 134565-04-1
Zn(C20H4N4(CH3)4(C2H5)2(C2H4COOC3H6C6H4N(CH3)2)(C2H4COOC2H4SC10H4O2(CH3)))

Conditions

Conditions	Yield
In methanol treatment of the ligand with a methanol soln. of zinc acetate;	100%

: AuC62H71N4C24H14N4C46H57CuC34H34N4O6(2+)*2PF6(1-)={AuC62H71N4C24H14N4C46H57CuC34H34N4O6}(PF6)2

: 557-34-6
zinc diacetate

: AuC62H71N4C24H14N2(ZnC46H55N4)CuC34H34N2O6(2+)*2PF6(1-)={AuC62H71N4C24H14N2(ZnC46H55N4)CuC34H34N2O6}(PF6)2

Conditions

Conditions	Yield
In methanol; dichloromethane refluxing of porphyrine with Zn(OAc)2 in CH2Cl2-MeOH for 1.5 h under argon; column chromy. (alumina);	100%

: 86119-84-8, 7664-38-2
phosphoric acid

: 557-34-6
zinc diacetate

: 7732-18-5
water

: 694-83-7
1,2-diaminocyclohexane

: Zn3(PO4)2(PO3OH)(H2-1,2-diaminocyclohexane)*2H2O

Conditions

Conditions	Yield
In water hydrothermal conditions, 180°C;	100%

...Expand

: boron phosphate

: 557-34-6
zinc diacetate

: 7732-18-5
water

: 694-83-7
1,2-diaminocyclohexane

: Zn3(PO4)2(PO3OH)(H2-1,2-diaminocyclohexane)*2H2O

Conditions

Conditions	Yield
In water hydrothermal conditions, molar ratio BPO4:Zn(OAc)2:diaminocyclohexane:water 2:1:2.5:117, , pH=8, 210°C; elem. anal.;	100%

...Expand

: trans-5,15-di(4-pyridyl)-10,20-diphenylporphyrin

: 557-34-6
zinc diacetate

: 159726-84-8
C42H26N6Zn

Conditions

Conditions	Yield
In methanol; chloroform dry N2-atmosphere; stirring, refluxing (10 h, dark); evapn. (vac.), washing (MeOH), drying;	100%

: C72H61N6BF2

: 557-34-6
zinc diacetate

: 214423-05-9
Zn(C72H59N6BF2)

Conditions

Conditions	Yield
In methanol	100%

: 107-97-1
sarcosine

: (C20H10N4((C4H9)2C6H3)3(C6H4))(C10H2N2O4)(C6H4)(CHO)

: 557-34-6
zinc diacetate

: 99685-96-8, 161105-99-3, 161106-00-9, 111138-12-6, 133318-63-5, 134053-11-5, 134931-35-4, 134931-36-5, 139703-76-7, 145633-27-8, 175414-73-0, 175414-74-1, 175414-75-2, 175519-12-7, 175519-13-8, 175519-14-9, 175519-15-0, 136376-46-0, 144906-37-6, 144906-38-7, 151767-00-9, 152882-97-8, 152882-98-9, 152882-99-0, 153062-34-1, 154171-74-1, 154171-75-2, 154333-99-0, 154334-00-6, 154397-63-4, 154460-59-0, 199456-56-9, 108739-25-9, 120329-57-9, 120329-58-0
fullerene-C60

: 201872-65-3
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(CH3NC2H3)C60)]

Conditions

Conditions	Yield
In toluene C60, C20H10N4((C4H9)2C6H3)3(C6H4)2(C10H2N2O4)(CHO), N-methylglycine (toluene) heated under N2 in dark for 6 h; cooled to 25°C, evapd. to dryness (reduced pressure); chromy. sepd., dissolved (CH3Cl), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from benzene-methanol;	100%

...Expand

: 5-(4-aminophenyl)-10,15,20-tris(3,5-di-tert-butylphenyl) porphyrin

: 89-32-7
Pyromellitic dianhydride

: 79098-13-8
4-hexadecylaniline

: 557-34-6
zinc diacetate

: 303955-50-2
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(C16H33))]

Conditions

Conditions	Yield
In N,N-dimethyl-formamide (C20H10N4((C4H9)2C6H3)3(C6H4))NH2, C10H2O6, (C16H33)NH(C6H5) (dry DMF) heated under N2 in dark for 22 h, cooled to 25°C, evapd. to dryness (reduced pressure); chromy., dissolved (CHCl3), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from chloroform-methanol;	100%

...Expand

: 5-[1'-(hexylaminomethyl)ferrocenyl]-10,15,20-tri(p-tolyl)porphyrin

: 557-34-6
zinc diacetate

: 838825-87-9
zinc(II) 5-[1'-(hexylaminomethyl)ferrocenyl]-10,15,20-tri(p-tolyl)porphyrin

Conditions

Conditions	Yield
In methanol; dichloromethane; water Fe(C5H4CH2NH(CH2)5CH3)(C5H4)-substituted porphyrin reacted with ZnOAc2 in CH2Cl2/MeOH/H2O for 10 h; chromy. (SiO2, CH2Cl2/MeOH); elem. anal.;	100%

: 5,10,15-triphenyl-20-(2,6-dimethyl-4[2-(trimethylsilyl)ethynyl]phenyl)porphyrin

: 557-34-6
zinc diacetate

: 184153-99-9
zinc(II) 5,10,15-triphenyl-20-(2,6-dimethyl-4-[2-(trimethylsilyl)ethynyl]phenyl)porphyrin

Conditions

Conditions	Yield
In chloroform reaction for 2.5 h;	100%

: [zinc(II) 5,10,15-triphenyl-20-porphinyl]-4'-[5,10,15-triphenyl-20-porphinyl]di(2,6-dimethylphenyl)ethyne

: 557-34-6
zinc diacetate

: ZnC20H8N4(C6H5)3C6H2(CH3)2CCC6H2(CH3)2ZnC20H8N4(C6H5)3

Conditions

Conditions	Yield
In chloroform reaction for 1 h;	100%

: [ZnC20N4H8(C6H5)3(C6H2(CH3)2CCC6H4C20N4H8H2(C6H2(CH3)3)3)]

: 557-34-6
zinc diacetate

: 184154-17-4
ZnC20H8N4(C6H5)3C6H2(CH3)2CCC6H4ZnC20H8N4(C6H2(CH3)3)3

Conditions

Conditions	Yield
In chloroform stirring (room temp., 1 h); filtration, concn.;	100%

: 2-hydroxy-5,10,15,20-tetrakis(3',5'-di-tert-butylphenyl)porphin

: 557-34-6
zinc diacetate

: 214962-06-8
[2-hydroxy-5,10,15,20-tetrakis(3',5'-di-tert-butylphenyl)porphinato]zinc(II)

Conditions

Conditions	Yield
With sodium hydride; Benzaldoxime In methanol; dichloromethane; mineral oil mixt. refluxing in dark for 45 min, solvent complete removal; residue chromy. (silica, DCM), recrystn. (DCM/MeOH);	100%

: [((((CH3)3C)2C6H3)3C20H10N4)C6H3(O(CH2)4CH3)CONHC6H2(OCH3)2NHCOC6H3(O(CH2)CH3)]2((((CH3)3C)2C6H3)2C20H10N4)

: 557-34-6
zinc diacetate

: [((((CH3)3C)2C6H3)3C20H8N4Zn)C6H3(O(CH2)4CH3)CONHC6H2(OCH3)2NHCOC6H3(O(CH2)CH3)]2((((CH3)3C)2C6H3)2C20H8N4Zn)

Conditions

Conditions	Yield
In methanol; dichloromethane reaction of zinc compd. with porphyrin deriv. in MeOH/CH2Cl2 at room temp. for 12 h;	100%

: diphenyl(10,20-diphenylporphyrin-5-yl)phosphine oxide

: 557-34-6
zinc diacetate

: 909039-64-1
diphenyl[10,20-diphenylporphyrinatozinc(II)-5-yl]phosphine oxide

Conditions

Conditions	Yield
In methanol; dichloromethane a soln. of zinc acetate in methanol was added to a soln. of porphyrin inCH2Cl2, the mixt. was refluxed for 2 h; ppt. was filtered, washed three times with methanol;	100%

: H2(C20H8N4(C6H4CH3)3)C6H4CH2NC6H4C(CH3)2COC6H3NO2CHCH

: 557-34-6
zinc diacetate

: 356527-60-1
Zn(C20H8N4(C6H4CH3)3)C6H4CH2NC6H4C(CH3)2COC6H3NO2CHCH

Conditions

Conditions	Yield
In chloroform (Ar); stirring a soln. of ligand with excess of zinc salt in CHCl3 overnight; column chromy (SiO2);	100%

: 557-34-6
zinc diacetate

: 147804-54-4
meso-pentyldipyrromethane

: 276885-27-9
5-formyl-1,1,3,3-tetramethylisoindolin-2-yloxyl

: 532379-02-5
5,10,15-tri-n-pentyl-20-(1',1',3',3'-tetramethylisoindolin-2'-yloxyl-5'-yl)porphyrinato zinc(II)

Conditions

Conditions	Yield
With trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone In methanol; dichloromethane; chloroform to soln. of 5-formyl-1,1,3,3-tetramethylisoindolin-2-yloxyl, 5-pentyldipyrromethane in CH2Cl2 under Ar, trifluoroacetic acid added, stirred for 20 min, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone added stirred, evapd. to dryness, chromy., refluxed,....; elem. anal.;	100%

...Expand

: pyropheophorbide a

: 557-34-6
zinc diacetate

: zinc 3-vinyl-8-ethyl-12-methyl-bacteriopheophorbide d

Conditions

Conditions	Yield
In chloroform excess of Zn(II) acetate, reflux;	100%

: (CH3)5(CH2)6(CH)5(C4N)3(C2NH2)(C)(CO)COOH(O)(C12H7)(CO)2

: 557-34-6
zinc diacetate

: (CH3)5(CH2)6(CH)5(C4N)3(C2N)(C)Zn(CO)COOH(O)(C12H7)(CO)2

Conditions

Conditions	Yield
In chloroform excess of Zn(II) acetate, reflux;	100%

: (CH3)10(CH2)14(CH)11(CO)3(2O)(C4N)3(4C)(NH2)(C12H7)(CO)2

: 557-34-6
zinc diacetate

: (CH3)10(CH2)14(CH)11(CO)3(2O)(C4N)3(4C)(N)(C12H7)(CO)2Zn

Conditions

Conditions	Yield
In chloroform excess of Zn(II) acetate, reflux;	100%

: C12H14O3

: 557-34-6
zinc diacetate

: Zn(C12H13O3)2

Conditions

Conditions	Yield
In dimethyl sulfoxide stirring; filtn., washing (DMSO, hot H2O, acetone), drying (60°C, 24 h); elem. anal.;	100%

Zinc acetate Consensus Reports

ZINC and its compounds are on the Community Right-To-Know List. Reported in EPA TSCA Inventory.

Zinc acetate Specification

The Zinc acetate is an organic compound with the formula C₄H₆O₄Zn. The IUPAC name of this chemical is zinc diacetate. With the CAS registry number 557-34-6, it is also named as acetic acid, zinc salt (2:1). The product's categories are Organic-metal Salt; Catalysis and Inorganic Chemistry; Chemical Synthesis; Zinc. Besides, it is a white crystalline powder, which is used as an astringent and weak antiseptic in medicine.

Physical properties about Zinc acetate are: (1)ACD/LogP: -0.29; (2)ACD/LogD (pH 5.5): -1.07; (3)ACD/LogD (pH 7.4): -2.86; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 2.73; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 2; (9)#H bond donors: 1; (10)Polar Surface Area: 37.3 Å²; (11)Flash Point: 40 °C; (12)Enthalpy of Vaporization: 23.7 kJ/mol; (13)Boiling Point: 117.1 °C at 760 mmHg; (14)Vapour Pressure: 13.9 mmHg at 25°C.

Preparation: this chemical can be prepared by zinc oxide and acetic acid. This reaction will need reagent hydrogen peroxide.

When you are using this chemical, please be cautious about it as the following:
It is highly flammable and harmful if swallowed. Please keep away from sources of ignition - No smoking. Besides, this chemical is irritating to eyes and very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. When you are using it, wear suitable protective clothing. This material and its container must be disposed of as hazardous waste.

You can still convert the following datas into molecular structure:
(1)SMILES: [Zn+2].[O-]C(=O)C.[O-]C(=O)C
(2)InChI: InChI=1/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
(3)InChIKey: DJWUNCQRNNEAKC-NUQVWONBAP
(4)Std. InChI: InChI=1S/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
(5)Std. InChIKey: DJWUNCQRNNEAKC-UHFFFAOYSA-L

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Source
mouse	LD50	intraperitoneal	57mg/kg (57mg/kg)	Toxicology and Applied Pharmacology. Vol. 49, Pg. 41, 1979.
rabbit	LDLo	intravenous	5mg/kg (5mg/kg)	Archives of Internal Medicine. Vol. 37, Pg. 641, 1926.
rat	LD50	oral	2510mg/kg (2510mg/kg)	Personal Communication from J.V. Marhold, VUOS, 539-18, Pardubice, Czechoslavakia, Mar. 29, 1977Vol. 29MAR1977,

Product Name

Zinc acetate

Synthetic route

Zinc acetate Consensus Reports

Zinc acetate Specification

Related Products

Hot Products