Cupric acetate supplier | CasNO.142-71-2

Name
Cupric acetate
EINECS 205-553-3
CAS No. 142-71-2
Article Data95
CAS DataBase
Density 1.068g/cm3
Solubility Soluble in water and alcohol. Slightly soluble in ether and glycerol.
Melting Point 115 °C
Formula C₄H₆CuO₄
Boiling Point 117.1 °C at 760 mmHg
Molecular Weight 363.27
Flash Point 40 °C
Transport Information UN 3077 9/PG 3
Appearance Green crystalline powder
Safety 26-60-61
Risk Codes 22-36/37/38-50/53
Molecular Structure
Hazard Symbols Xn, N
Synonyms Aceticacid, copper(2+) salt (8CI,9CI);Copper acetate (Cu(OAc)2) (7CI);Acetic acidcupric salt;Copper acetate (Cu(C2H3O2)2);Copper acetate(Cu(MeCO2)2);Copper diacetate;Copper(2+) acetate;Copper(2+) diacetate;Copper(II) acetate;Crystallized verdigris;Crystals of Venus;Cupric diacetate;Neutral verdigris;Venus copper;
PSA 37.30000
LogP 0.08840

Synthetic route

: copper(II) nitrate trihydrate

: 108-24-7
acetic anhydride

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In acetic anhydride reflux; washed with acetic anhydride and ether;;	93%
In acetic anhydride reflux; washed with acetic anhydride and ether;;	93%
In neat (no solvent) on warming;;
In neat (no solvent) on warming;;

: [Cu(NO2)(OCHC6H4P(C6H5)2)2]

: 64-19-7
acetic acid

A: 142-71-2
copper diacetate

B: 10102-44-0
Nitrogen dioxide

Conditions

Conditions	Yield
In dichloromethane N2, acid added at room temp.;	A n/a B 85%

...Expand

: 108-24-7
acetic anhydride

A: diacetyl-orthonitric acid

B: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With copper(II) nitrate at 30 - 35℃;

: 108-24-7
acetic anhydride

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With copper(II) nitrate

: 108-24-7
acetic anhydride

Cu(NO3)2+3H2O: Cu(NO3)2+3H2O

A: diacetyl-orthonitric acid

B: 142-71-2
copper diacetate

Conditions

Conditions	Yield
at 30 - 45℃;

...Expand

: 75-15-0
carbon disulfide

: 938-81-8
N-nitrosoacetanilide

copper: copper

: 142-71-2
copper diacetate

...Expand

: 56-23-5
tetrachloromethane

: 938-81-8
N-nitrosoacetanilide

copper: copper

A: 142-71-2
copper diacetate

B copper (II)-ion: copper (II)-ion

C copper chloride: copper chloride

...Expand

Cu(C2H3O2)2+2 NH3: Cu(C2H3O2)2+2 NH3

: 142-71-2
copper diacetate

Cu(C2H3O2)2+H2O: Cu(C2H3O2)2+H2O

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With toluene azeotrope Destillation;

: copper(II) acetate tetrahydrate

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent, solid phase) byproducts: H2O; acetate was heated in vac. at 150°C for 3 h;

: 64-19-7
acetic acid

: copper(II) oxide

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In not given CH3CO2H passed over CuO at 230°C; CuO obtained by heating Cu(NO3)2 to red heat;;
In not given CH3CO2H passed over CuO at 230°C; CuO obtained by heating Cu(NO3)2 to red heat;;

: 12775-96-1, 15158-11-9, 15721-63-8, 16941-75-6, 17493-86-6, 19498-52-3, 20499-83-6, 20499-84-7, 20499-85-8, 20499-86-9, 20573-10-8, 20573-11-9, 21595-51-7, 21595-52-8, 22206-52-6, 26445-28-3, 28959-95-7, 37362-93-9, 39417-05-5, 54603-16-6, 54603-23-5, 54603-32-6, 54603-40-6, 54603-48-4, 54603-81-5, 54603-89-3, 56316-56-4, 95985-91-4, 122297-32-9, 7440-50-8
copper

: 64-19-7
acetic acid

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In nitric acid aq. HNO3; Dissolving copper metal in a mixt. of HNO3 and distd. water followed twice by evapn. to near dryness and addn. of a mixt. of acetic acid and distd. water.; Not isolated.;

: copper(II) carbonate

: 64-19-7
acetic acid

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In acetic acid treatment of CuCO3 with CH3COOH; recrystn. from aq. methanol, drying;
In acetic acid Cu(II) carbonate treated with acetic acid according to Prabhumirashi, L.S., Khoje J. K., Thermochim Acta, 383 (2002) 109;

: 20427-59-2
copper hydroxide

: 64-19-7
acetic acid

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent)
In neat (no solvent)

: 12775-96-1, 15158-11-9, 15721-63-8, 16941-75-6, 17493-86-6, 19498-52-3, 20499-83-6, 20499-84-7, 20499-85-8, 20499-86-9, 20573-10-8, 20573-11-9, 21595-51-7, 21595-52-8, 22206-52-6, 26445-28-3, 28959-95-7, 37362-93-9, 39417-05-5, 54603-16-6, 54603-23-5, 54603-32-6, 54603-40-6, 54603-48-4, 54603-81-5, 54603-89-3, 56316-56-4, 95985-91-4, 122297-32-9, 7440-50-8
copper

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With acetic acid In not given 5% acetic acid;	>99
With acetic acid In not given 5% acetic acid;	>99

: 6046-93-1
copper(II) acetate monohydrate

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
at 140°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;
In neat (no solvent) heating to 90°C;;

: copper(II) acetate hydrate

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent) 110°C, vac.;
In acetic anhydride 24 h, refluxing, dry atmosphere; filtration, washing (Et2O), drying (8 h, 100°C, vac.);

: {Cu(C5H5N)4}(2+)*2CH3CO2(1-)={Cu(C5H5N)4}(CH3CO2)2

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In not given

: Cu(2+)*NC5H4COC6H5*2CH3CO2(1-)=Cu(NC5H4COC6H5)(CH3CO2)2

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent) Kinetics; byproducts: 4-benzoylpyridine; thermal decompn. at 215°C;;

: tetrakis(acetato)diaquadicopper(II)

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In acetic anhydride 3 h, excess of Ac2O, refluxing; filtn., washing (CH2Cl2), drying (vac.);

: 20427-59-2
copper hydroxide

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With acetic acid In acetic acid copper hydroxide dissoln.;
With acetic acid In water pH 5-6; evapn. (70°C), drying (70°C); elem. anal.;

: Cu(2+)*2CH3CO2(1-)*CH3CO2H=CuH(CH3CO2)3

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent) at 50°C;;
In neat (no solvent) at 50°C;;

: Cu(2+)*(CH3COO)(1-)*C10H6NO2(1-)=Cu(C10H6NO2)(CH3COO)

A: 7250-53-5
quinoline-5-carboxylic acid

B: Cu(2+)*C10H6NO2(1-)*OH(1-)=Cu(OH)(C10H6NO2)

C: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With water In water hydrolysis;;
With H2O In water hydrolysis;;

...Expand

: azurite

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With acetic acid 5% acetic acid;	>99
With acetic acid leaching with 5% acetic acid;	>99
With acetic acid 5% acetic acid;	>99

: 137129-35-2, 27528-47-8
N-(pyridine-2-ylethyl)-2-hydroxy-benzylideneamine

: copper dichloride

: 646503-98-2, 55314-79-9
(Cu(C5H4NCH2CH2NCHC6H4O)2)

B: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In methanol under Ar; MeOH soln. of ligand, CuCl2 and NaOH (molar ratio 1:1:1) heated under reflux for 3 h; cooled to room temp.; recrystd. from MeOH under Ar;

...Expand

: 6046-93-1
copper(II) acetate monohydrate

A: ammonium acetate

B: 2Cu(2+)*4CH3CO2(1-)*Cu(OH)2*5H2O=2Cu(CH3CO2)2*Cu(OH)2*5H2O

C: 142-71-2
copper diacetate

Conditions

Conditions	Yield
With ammonium hydroxide In water heating to 90°C;;
With aq. NH3 In water heating to 90°C;;

...Expand

: 2Cu(2+)*4CH3CO2(1-)*Cu(OH)2*5H2O=2Cu(CH3CO2)2*Cu(OH)2*5H2O

A: 142-71-2
copper diacetate

B: 20427-59-2
copper hydroxide

Conditions

Conditions	Yield
at ambient temp.;;
at ambient temp.;;

: blue verdigris = Blauer Gruenspan (germ.) = vert-de-gris

: 142-71-2
copper diacetate

Conditions

Conditions	Yield
In neat (no solvent) dry distn.;;

: 165681-92-5
[((CH3)3SiC2Si(CH3)3)[Cu(μ-acetate)]2]2

A: 142-71-2
copper diacetate

B: 12775-96-1, 15158-11-9, 15721-63-8, 16941-75-6, 17493-86-6, 19498-52-3, 20499-83-6, 20499-84-7, 20499-85-8, 20499-86-9, 20573-10-8, 20573-11-9, 21595-51-7, 21595-52-8, 22206-52-6, 26445-28-3, 28959-95-7, 37362-93-9, 39417-05-5, 54603-16-6, 54603-23-5, 54603-32-6, 54603-40-6, 54603-48-4, 54603-81-5, 54603-89-3, 56316-56-4, 95985-91-4, 122297-32-9, 7440-50-8
copper

Conditions

Conditions	Yield
In not given N2 atmosphere;

: 142-71-2
copper diacetate

: 85281-73-8
(3S,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)-ethyl]-4-phenylthio-2-azetidinone

: 76899-07-5, 78963-47-0, 78963-48-1, 78963-60-7, 80951-41-3, 81275-02-7, 85647-75-2, 85954-95-6, 92217-74-8, 104527-11-9, 76855-69-1
(3R,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-acetoxyazetidin-2-one

Conditions

Conditions	Yield
With acetic acid at 100℃; for 0.75h;	100%
at 100℃; for 0.75h;

: 554-95-0
benzene-1,3,5-tricarboxylic acid

: 142-71-2
copper diacetate

: basolite C300

Conditions

Conditions	Yield
for 0.166667h;	100%
In ethanol deposition on colloidal polystyrene crystal array;

: 55-22-1
pyridine-4-carboxylic acid

: 142-71-2
copper diacetate

: copper(II) isonicotinate

Conditions

Conditions	Yield
for 0.166667 - 6h; Product distribution / selectivity; Neat (no solvent); Mechanochemistry;	100%

: 142-71-2
copper diacetate

: 28492-94-6, 101306-61-0
isatin-4-phenyl thiosemicarbazone

: copper(iptsc)2

Conditions

Conditions	Yield
Refluxing of Schiff base and metal acetate in 2:1 molar ratio for 2-4 h.; Filtn. of resulting complex, washing, drying and collecting at room temp., elem. anal.;	100%

: 917-23-7
5,10,15,20-tetraphenyl-21H,23H-porphine

: 142-71-2
copper diacetate

: 14172-91-9
(tetraphenylporphyrin)copper(II)

Conditions

Conditions	Yield
In solid High Pressure; 2000 MPa at room temp.; extrd. (chloroform), chromy.(alumina); UV;	100%
In 1,4-dioxane refluxing of C44H30N4 and copper(II) acetate in dioxane for 2.5 h;; evapn. in vac.; chromy. (trichloroethylene); recrystn. from CHCl3/methanol;;	86%
In 1,4-dioxane refluxing of C44H30N4 and copper(II) acetate in dioxane for 2.5 h;; evapn. in vac.; chromy. (trichloroethylene); recrystn. from CHCl3/methanol;;	86%

: 14167-20-5, 1160066-31-8
nickel(II) salen

: 142-71-2
copper diacetate

: 14167-15-8
N,N'-ethylenebis(salicylideneiminato)copper(II)

Conditions

Conditions	Yield
In pyridine Kinetics; boiling pyridine;	100%
In pyridine Kinetics; boiling pyridine;	100%

: meso-tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)porphyrin

: 142-71-2
copper diacetate

: 5,10,15,20-tetrakis(3,5-di-t-butyl-4-hydroxyphenyl)porphyrininatocopper(II)

Conditions

Conditions	Yield
In methanol to ligand in boiling CHCl3 is added a saturated soln. of Cu(OAc)2 in MeOH, mixt. is refluxed for 1 h; evapn., residue is dissolved in CHCl3 and the soln. is loaded on a neutral alumina column, eluated by CHCl3, eluate is evapd. and MeOH is added, crystals are filtered and air-dried, elem. anal.;	100%

: 142-71-2
copper diacetate

: 74619-49-1
3,5-bis-(o-hydroxyphenyl)-1,2,4-oxadiazole

: 110981-83-4
Cu(2+)*C2N2O(C6H4O)2(2-)=Cu(C2N2O(C6H4O)2)

Conditions

Conditions	Yield
In methanol; propan-1-ol adding the acetate in a min. vol. of hot MeOH to a soln. of the ligand in propanol, boiling until the cryst. product appears (5 - 10 min); cooling, filtering, washing (EtOH), drying (vac., 100°C); elem. anal.;	100%

: 170660-32-9
C15H15NO2

: 142-71-2
copper diacetate

: 170660-38-5
[CuC15H13NO2]2

Conditions

Conditions	Yield
In methanol stirring, (reflux, 2-3 h); concn., cooling, filtn., recryst. (MeOH), drying (air); elem. anal.;	100%

: C12H14O3

: 142-71-2
copper diacetate

: Cu(C12H13O3)2

Conditions

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

: (C10H5(OH)2CHN)2C6H2(OC12H25)2

: 7732-18-5
water

: 142-71-2
copper diacetate

: (C10H5(OH)OCHN)2C6H2(OC12H25)2Cu*H2O

Conditions

Conditions	Yield
In tetrahydrofuran; methanol ligand in THF added dropwise to CH3OH soln. of Cu salt (1.1 equiv.), treated with CH3OH, reacted for 16 h; elem. anal.;	100%

...Expand

: 142-71-2
copper diacetate

: 307494-24-2
(S)-N-(5-nitro-salicylidene)-2-amino-1,1-di-(5-tert-butyl-2-butoxy-phenyl)-propan-1-ol

: 374934-47-1
[(2S)-N-(5-nitrosalicylidene)-2-amino-1,1-di(5-tert-butyl-2-n-butoxyphenyl)-1-propanol] copper complex

Conditions

Conditions	Yield
In toluene at 80℃; for 5h; Product distribution / selectivity;	100%

: 5,10,15,20-tetramesitylporphyrin

: 142-71-2
copper diacetate

: 107556-84-3
Cu(5,10,15,20-tetramesitylporphyrin)

Conditions

Conditions	Yield
	100%

: C45H40N4

: 142-71-2
copper diacetate

: C45H38CuN4

Conditions

Conditions	Yield
In methanol; dichloromethane Inert atmosphere; Heating;	100%

: 1449486-20-7
C35H24N2

: 142-71-2
copper diacetate

: 1449491-31-9
C70H46CuN4

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; Darkness;	100%

: C49H48N6O4

: 142-71-2
copper diacetate

: 1476064-39-7
3,12-(NO2)2TtBuPCorrCu

Conditions

Conditions	Yield
In methanol; chloroform for 0.5h; Reflux;	100%

: (R)-N,N′-bis(3,5-di-tert-butyl-2-hydroxybenzyl)-1,2-diaminobicyclo[2.2.2]octane

: 142-71-2
copper diacetate

: C38H58CuN2O2

Conditions

Conditions	Yield
In ethanol at 20℃;	100%

: 5‐bromo‐2‐(5-(2‐(4‐bromo-2-hydroxybenzylidene)hydrazineyl)‐4‐nitro‐2,3‐dihydro‐1H‐pyrazol‐3‐yl)phenol

: 142-71-2
copper diacetate

: C16H11Br2N5O4(2-)*Cu(2+)

Conditions

Conditions	Yield
In dimethyl sulfoxide at 80℃; for 8h;	100%

: 142-71-2
copper diacetate

: 161265-03-8
4,5-bis(diphenylphosphino)-9,9-dimethylxanthene

: C43H38CuO5P2

Conditions

Conditions	Yield
In tetrahydrofuran	100%

: 142-71-2
copper diacetate

: C9H21Si(1+)*C24BF20(1-)

: 75-05-8
acetonitrile

: [Cu(NCCH3)6][B(C6F5)4]2

Conditions

Conditions	Yield
at 20℃; for 5h;	100%

...Expand

: 142-71-2
copper diacetate

: 2,2'-(1,8-dithia-4,11-diazacyclotetradecane-4,11-diyl)diacetic acid dihydrochloride

: 2,2'-(1,8-dithia-4,11-diazacyclotetradecane-4,11-diyl)diacetate copper(II)

Conditions

Conditions	Yield
Stage #1: copper diacetate; 2,2'-(1,8-dithia-4,11-diazacyclotetradecane-4,11-diyl)diacetic acid dihydrochloride In water; acetonitrile at 23℃; for 0.166667h; Inert atmosphere; Stage #2: In water; acetonitrile at 23℃; for 0.0833333h; Inert atmosphere; Sonication;	100%

: 142-71-2
copper diacetate

: 149-30-4
2-Mercaptobenzothiazole

: bis(2-mercaptobenzothiazolato)copper(II)

Conditions

Conditions	Yield
In methanol Milling; Green chemistry;	99.3%

: 5-(4-bromophenyl)-15-[1,5-bis(dimethoxyphosphoryloxy)pent-3-yl]porphyrin

: 142-71-2
copper diacetate

: Cu(II)-5-(4-bromophenyl)-15-[1,5-bis(dimethoxyphosphoryloxy)pent-3-yl]porphyrin

Conditions

Conditions	Yield
In methanol; chloroform at 20℃; for 12h;	99%

: meso-tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)porphyrin

: 142-71-2
copper diacetate

: Cu(II)(tetra(4-hydroxy-3,5-di-tert-butylphenyl)porphine)

Conditions

Conditions	Yield
In N,N-dimethyl-formamide heated under Ar; UV;	99%

: 351325-54-7
(C6H5)4(CH3(CH2)3)(C5H2N)4H3O2

: 142-71-2
copper diacetate

: ((C6H5)4(CH3(CH2)3)(C5H2N)4HO2)Cu

Conditions

Conditions	Yield
In methanol; dichloromethane a ligand in boiling CH2Cl2 was treated with excess of Cu acetate in warmMeOH; soln. washed with water and dried over Na2SO4;	99%

: ammonium hexafluorophosphate

: 142-71-2
copper diacetate

: 177779-89-4
1,3-bis[4-(4-tert-butylphenyl)-2,2':6',2''-terpyridin-6-yl]benzene

: Cu2(C56H48N6)2(4+)*4PF6(1-) = [Cu2(C56H48N6)2](PF6)4

Conditions

Conditions	Yield
In methanol refluxing the Cu salt and the ligand in MeOH for 30 min, filtration, addn. of satd. methanolic NH4PF6; recrystn. by diffusion of Et2O into a MeCN soln.; elem. anal.;	99%

...Expand

: (H2(C6F5)3(C5H2N)2C5HNO)2

: 142-71-2
copper diacetate

: 500116-50-7
[(C30H10N6O2)(C6F5)6]Cu2

Conditions

Conditions	Yield
In dichloromethane hexaphyrin was treated with anhyd. Cu(II) acetate in CH2Cl2 soln.;	99%

: 2N((CH2)3CH3)4(1+)*Mo2O5(O2C6H2(NCHC6H3(OC2H5)OH)2)2(2-)=[N((CH2)3CH3)4]2[Mo2O5(O2C6H2(NCHC6H3(OC2H5)OH)2)2]

: 142-71-2
copper diacetate

: 2N((CH2)3CH3)4(1+)*Mo2O5(Cu(O2C6H2(NCHC6H3(OC2H5)O)2))2(2-)=[N((CH2)3CH3)4]2[Mo2O5(Cu(O2C6H2(NCHC6H3(OC2H5)O)2))2]

Conditions

Conditions	Yield
In methanol stoich. amts., room temp.;	99%

: 13755-29-8
sodium tetrafluoroborate

: [(dppm)2Ru(S2CNC4H8NCS2)]

: 142-71-2
copper diacetate

: [(Ru(bis(diphenylphosphino)methane)2(S2CNC4H8NCS2))2Cu](BF4)2*dichloromethane

Conditions

Conditions	Yield
In dichloromethane stoich. mixt.; elem. anal.;	99%

...Expand

: meso-heptakis(pentafluorophenyl)[32]heptaphyrin

: 142-71-2
copper diacetate

: (C4H2NC(C6F5))2H2NC4H2(C(C6F5))2(C4H2NCC6F5)3C4H2NCu

Conditions

Conditions	Yield
In methanol at room temp.;	99%

Cupric acetate History

Copper(II) acetate (CAS NO.142-71-2) is occasionally the primary component of verdigris, the blue-green substance that forms on copper during long exposures to atmosphere. It was historically prepared in vineyards, since acetic acid is a byproduct of fermentation.Copper (cupric) acetate tablets were believed to repel sharks in the mid twentieth century.

Cupric acetate Consensus Reports

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

Cupric acetate Standards and Recommendations

ACGIH TLV: TWA 1 mg(Cu)/m³

Cupric acetate Specification

The IUPAC name of this chemical is copper diacetate. With the CAS registry number 142-71-2, it is also named as Acetate de cuivre. The product's categorie is organic-metal salt. It is green crystalline powder which is soluble in water and ethanol, slightly soluble in ether and glycerol. In addition, it is highly toxic and the storage environment should be ventilate, low-temperature and dry. Keep Copper(II) acetate separate from acids.

The other characteristics of this product can be summarized as: (1)ACD/LogP: -0.29; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.07; (4)ACD/LogD (pH 7.4): -2.86; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 2.73; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 0; (12)Flash Point: 40 °C; (13)Enthalpy of Vaporization: 23.7 kJ/mol; (14)Boiling Point: 117.1 °C at 760 mmHg; (15)Vapour Pressure: 13.9 mmHg at 25°C; (16)Exact Mass: 180.95621; (17)MonoIsotopic Mass: 180.95621; (18)Topological Polar Surface Area: 80.3; (19)Heavy Atom Count: 9; (20)Complexity: 25.5.

Preparation of Copper(II) acetate: It has been synthesized for centuries by the method described in the history section. The overall reaction is as follows:
2 CuSO₄.5H₂O + 4 NH₃ + 4 C₂H₄O → Cu₂(OAc)₄(H₂O)₂ + 2 (NH₄)₂SO₄ + 8 H₂O
The hydrate form can be dehydrated by heating at 100 °C in a vacuum:
Cu₂(OAc)₄(H₂O)₂ → Cu₂(OAc)₄ + 2 H₂O
Heating a mixture of anhydrous Cu₂(OAc)₄ and copper metal affords colorless, volatile cuprous acetate:
2 Cu + Cu₂(OAc)₄ → 4 CuOAc

Uses of Copper(II) acetate: It is used as an insecticide, in the preparation of other chemicals, as a fungicide, and mildew preventive, fungicides, printing and dyeing fixing agent. And it also has been used as intermediate to prepare Paris green.

When you are using this chemical, please be cautious about it as the following:
It is not only harmful if swallowed, but also irritating to eyes, respiratory system and skin. And it is also very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. This material and its container must be disposed of as hazardous waste. Additionally, people should avoid release to the environment.

People can use the following data to convert to the molecule structure.
1. SMILES:[Cu+2].[O-]C(=O)C.[O-]C(=O)C
2. InChI:InChI=1/2C2H4O2.Cu/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
3. InChIKey:OPQARKPSCNTWTJ-NUQVWONBAO

The following are the toxicity data which has been tested.

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LD50	intraperitoneal	2500ug/kg (2.5mg/kg)		Biochemical Pharmacology. Vol. 30, Pg. 771, 1981.
mouse	LD50	intravenous	20mg/kg (20mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991.
mouse	LD50	oral	196mg/kg (196mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991.
rabbit	LDLo	oral	250mg/kg (250mg/kg)		Journal of Medical Research. Vol. 42, Pg. 461, 1919.
rat	LD50	intraperitoneal	14700ug/kg (14.7mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991.
rat	LD50	intravenous	17100ug/kg (17.1mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991.
rat	LD50	oral	501mg/kg (501mg/kg)	BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD	Indian Journal of Pharmacology. Vol. 23, Pg. 153, 1991.
rat	LD50	subcutaneous	350mg/kg (350mg/kg)	MUSCULOSKELETAL: JOINTS	Progress in Medical Chemistry. Vol. 15, Pg. 211, 1977.

Product Name

Cupric acetate

Synthetic route

Cupric acetate History

Cupric acetate Consensus Reports

Cupric acetate Standards and Recommendations

Cupric acetate Specification

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