Mercury acetate supplier | CasNO.1600-27-7

Name
MERCURIC ACETATE
EINECS 216-491-1
CAS No. 1600-27-7
Article Data47
CAS DataBase
Density 3.29 g/cm³
Solubility Soluble in water.
Melting Point 179-182 °C(lit.)
Formula C₂H₄O₂.1/2Hg
Boiling Point 117.1 °C at 760 mmHg
Molecular Weight 318.679
Flash Point 40 °C
Transport Information UN 1629 6.1/PG 2
Appearance white or off-white powder
Safety 13-28-36-45-60-61
Risk Codes 26/27/28-33-50/53
Molecular Structure
Hazard Symbols T+, N
Synonyms Aceticacid, mercuridi- (7CI);Acetic acid, mercury(2+) salt (8CI,9CI);Bis(acetyloxy)mercury;Diacetoxymercury;Mercuric acetate;Mercuric diacetate;Mercuric(II) acetate;Mercury acetate (Hg(O2C2H3)2);Mercurydiacetate;Mercury(2+) acetate;Mercury(II) acetate;Mercury(II) diacetate;
PSA 80.26000
LogP -2.49010

Synthetic route

: 64-19-7
acetic acid

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With mercury(II) oxide

: 108-24-7
acetic anhydride

mercuri fluoride: mercuri fluoride

A: 557-99-3
acetyl fluoride

B: 1600-27-7
mercury(II) diacetate

...Expand

: 108-24-7
acetic anhydride

Millon's base: Millon's base

A: 1600-27-7
mercury(II) diacetate

B: 631-61-8
ammonium acetate

C: 64-19-7
acetic acid

...Expand

: 64-19-7
acetic acid

: mercury(II) oxide

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
Heating / reflux;
In water at 50℃;
at 50℃;

: 748084-55-1
mercuric carbonate

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With acetic acid In acetic acid
With acetic acid In acetic acid aq. acetic acid;

: mercury(II) oxide

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With acetic acid In acetic acid on water bath; filtered, cooled, washed with ethyl acetate, recrystd., drying above CaCl2 in vacuum;
With acetic acid In acetic acid washed with chloroform, drying above caustic soda in vacuum;
With acetic acid In acetic acid aq. acetic acid; on water bath; filtered, cooled, washed with ethyl acetate, recrystd., drying above CaCl2 in vacuum;
With glacial acetic acid In acetic acid washed with chloroform, drying above caustic soda in vacuum;

: 127-08-2
potassium acetate

: mercury(II) nitrate

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In not given byproducts: KNO3;
In not given byproducts: KNO3;

: mercury

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With CH3COOH; H2O2; nitric acid In not given refluxed 40°C, mixed with H2O2, 80°C 30 min, evaporated at ambient temp. and vacuum;
With dihydrogen peroxide; acetic acid; nitric acid In not given refluxed 40°C, mixed with H2O2, 80°C 30 min, evaporated at ambient temp. and vacuum;

: 79-21-0
peracetic acid

: mercury

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In acetic acid	>99
In acetic acid	>99

: mercury(II) nitrate

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With acetic anhydride 4-5-fold excess of (CH3CO)2O;
With acetic anhydride 4-5-fold excess of (CH3CO)2O;

: 127-09-3
sodium acetate

: mercury(II) nitrate

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With nitric acid In water Hg(NO3)2 acidified with HNO3;
With HNO3 In water Hg(NO3)2 acidified with HNO3;

: H2C[C(Me)N(C6H3-2,6-iPr2)]2

: HgC6F5(1+)*CH3COO(1-)=Hg(C6F5)OCO(CH3)

A: 1600-27-7
mercury(II) diacetate

B: 973-17-1
bis(pentafluorophenyl)mercury(II)

Conditions

Conditions	Yield
In further solvent(s) all manipulations by Schlenk technique; no reaction even in molar ratio of Hg compd.:org. compd. 1:2, only dismutation;

...Expand

: 631-60-7
mercury(I) acetate

A: 1600-27-7
mercury(II) diacetate

B: mercury

Conditions

Conditions	Yield
In pyridine disproportion in pyridine;
In water Irradiation (UV/VIS); heating;
In water Irradiation (UV/VIS); heating;
In pyridine disproportion in pyridine;

: mercury(II) fluoride

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
With acetic anhydride In acetic anhydride

: 631-60-7
mercury(I) acetate

A: 1600-27-7
mercury(II) diacetate

B: 108-07-6
methyl mercury acetate

C: mercury

Conditions

Conditions	Yield
In acetic acid Irradiation (UV/VIS);
In acetic acid Irradiation (UV/VIS);

...Expand

: 37082-85-2
(HgCN)(1+)*(CH3CO2)(1-)={HgCN}CH3CO2

A: 1600-27-7
mercury(II) diacetate

B: mercury(II) cyanide

Conditions

Conditions	Yield
With H2O
With water

: 71-50-1
acetate

: mercury ion

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In water Kinetics; equil.; equil. constant given;;
In water Kinetics; equil.; equil. constant given;;

: mercury ion

: 127-08-2
potassium acetate

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In not given

: C5H5Mo(CO)3Hg(η2-O2CCH3)

A: ((η5-C5H5)(CO)3Mo)2Hg

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene under N2, kept for several hours at room temp.;

: 1162-06-7
triphenyllead acetate

: mercury

: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In dichloromethane Electrolysis; controlled potential oxidative electrolysis at a Hg pool electrode in CH2Cl2 at 20°C in the presence of 0.1 M Bu4NClO4; further unidentified products; not isolated;

: 84839-07-6
[(acetoxymercuriothio)methyl]triethylsilane

A: ((C2H5)3Si(CH2)S)2Hg

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene dilute soln.;

: 84839-12-3
C2H3O2(1-)*C4H11O3SSi(1-)*Hg(2+)

A: bis[(trimethoxysilyl)methylthio]mercury

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene dilute soln.;

: 84839-14-5
C2H3O2(1-)*C6H15O3SSi(1-)*Hg(2+)

A: ((CH3O)3Si(CH2)3S)2Hg

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene dilute soln.;

: 84839-13-4
C2H3O2(1-)*C5H13O3SSi(1-)*Hg(2+)

A: ((CH3O)3Si(CH2)2S)2Hg

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene dilute soln.;

: 84839-09-8
C2H3O2(1-)*C9H21SSi(1-)*Hg(2+)

A: ((C2H5)3Si(CH2)3S)2Hg

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In benzene dilute soln.;

: (HgO2CCH3)4CP2(C6H5)4(2+)*2CF3SO3(1-)

A: (HgO2CCH3)3CHP2(C6H5)4(2+)*2CF3SO3(1-)*3CH3SOCH3

B: 1600-27-7
mercury(II) diacetate

Conditions

Conditions	Yield
In not given decomp. in soln.;;

: 1600-27-7
mercury(II) diacetate

: 122714-12-9
2,3,6-tri-O-benzoyl-4-deoxy-α-D-xylo-hexopyranosyl chloride

: 122714-13-0
1-O-acetyl-2,3,6-tri-O-benzoyl-4-deoxy-β-D-xylo-hexopyranose

Conditions

Conditions	Yield
In acetic acid for 1h; Ambient temperature;	100%

: 1600-27-7
mercury(II) diacetate

: bis(thioacetanilide)mercury(II)

A: 637-53-6
thioacetanilide

B: 1563-87-7
N-acetyl-N-phenylacetamide

Conditions

Conditions	Yield
In dichloromethane for 3h; Ambient temperature;	A n/a B 100%

...Expand

: 67-56-1
methanol

: 1600-27-7
mercury(II) diacetate

: 631-60-7
mercury(I) acetate

Conditions

Conditions	Yield
trifluoroborane diethyl ether In methanol 0.2 Mol catalysts, in 0.2 molar soln., 24h, 50°C;	100%
trifluoroborane diethyl ether In methanol 0.2 Mol catalysts, in 0.2 molar soln., 24h, 50°C;	100%
perchloric acid In methanol 0.34 Mol HClO4, in 0.2 molar soln., 70h, 50°C;	60%

: 13688-78-3
4-methylbenzenetrifluorosilane

: 1600-27-7
mercury(II) diacetate

: 2440-35-9
p-CH3-C6H4-Hg-CH3CO2

Conditions

Conditions	Yield
In benzene addn. of 4-CH3-PhSiF3 to suspn. of HgAc2, mixt. heated (5 min, 80°C); cooled, filtered;	100%

: 1,2-dimethoxyethanebis(pentadeuterocyclopentadienyl)ytterbium(II)

: 1600-27-7
mercury(II) diacetate

: di-μ-acetato-tetrakis(cyclopentadienyl)diytterbium(III)

Conditions

Conditions	Yield
In tetrahydrofuran byproducts: Hg, dme; react. at room temp. for 16 h under N2; suspn. filtered, filter washed (THF), filtrate and washings evapd. (vac.); elem. anal.;	100%

: 368-47-8
phenyltrifluorosilane

: 1600-27-7
mercury(II) diacetate

: 62-38-4
phenylmercuric acetate

Conditions

Conditions	Yield
In benzene byproducts: F3SiOCOCH3; addn. of PhSiF3 to suspn. of HgAc2, mixt. heated ( 10-15 min, 80°C); cooled, filtered;	100%
In benzene byproducts: F3SiOCOCH3; suspn. of HgAc2 in benzene treated with PhSiF3, after 10-15 min heated to boiling; crystn. upon cooling;	100%
In benzene byproducts: F3SiOCOCH3; react. of starting materials in soln. at 25°C for 2h;	99%

: 157-33-5
bicyclo[1.1.0]butane

: 1600-27-7
mercury(II) diacetate

: 57297-71-9
1-acetoxymercuri-3-acetoxycyclobutane

Conditions

Conditions	Yield
In dichloromethane addn. of bicylobutane to suspn. of Hg(OAc)2 in CH2Cl2 (stirring), stirring (30 min); removal of solvent (evapn.);	100%

: 62830-22-2
ortho-biphenylenemercury trimer

: 1600-27-7
mercury(II) diacetate

: 71445-59-5
C12H8(HgO2CCH3)2

Conditions

Conditions	Yield
In methanol the biphenylenemercury suspensed in boiling methanol; mercuric acetate added until all the trimer had dissolved; a little more trimer was added; filtration; evaporation to a small volume; crystals washed quickly withcold glacial acetic acid and copious amounts of distilled water; dried at 80°C; elem. anal.;	100%
In 1,2,5-trimethyl-benzene refluxed in boiling mesitylene for 30 min; solvent was partially evaporated; cooled; further evaporation of the filtrate;	0%

: 93680-30-9
HN4CN3(H)C6H4Br

: 1600-27-7
mercury(II) diacetate

: 108054-30-4
[Hg(N4C)N=NNC6H4Br](n)

Conditions

Conditions	Yield
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;;	100%

HN4CN3(H)C6H4Cl: 93680-29-6
HN4CN3(H)C6H4Cl

: 1600-27-7
mercury(II) diacetate

: 108054-29-1
[Hg(N4C)N=NNC6H4Cl](n)

Conditions

Conditions	Yield
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;;	100%

: 93680-31-0
HN4CN3(H)C6H4NO2

: 1600-27-7
mercury(II) diacetate

: 108054-31-5
[Hg(N4C)N=NNC6H4NO2](2-)

Conditions

Conditions	Yield
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;;	100%

: 18441-99-1
(triethylsilyl)methanethiol

: 1600-27-7
mercury(II) diacetate

: 84839-07-6
[(acetoxymercuriothio)methyl]triethylsilane

Conditions

Conditions	Yield
In tetrahydrofuran byproducts: CH3COOH; stirring (1 h, room temp.); solvent driving off (rotary evaporator), residue diln. (benzene), unchanged Hg-acetate filtration off, benzene and acetic acid evapn. (vac.) from filtrate, residue (thick oil) crystn. during 1 d; elem. anal.;	100%

: [2,6-bis(dimethylaminomethyl)-1-phenyl]platinium bromide

: 1600-27-7
mercury(II) diacetate

: [(o,o'-(Me2NCH2)2C6H3)(MeCO2)(μ-MeCO2)PtHgBr]

Conditions

Conditions	Yield
In chloroform	100%

: cis-bis{2-(dimethylaminomethyl)phenyl}platinum(II)

: 1600-27-7
mercury(II) diacetate

: rac-a-(μ-acetato-O,O')-b-(O-acetatomercurio)-cf,de-bis[2-(dimethylaminomethyl)-phenyl-N,C]platinum

Conditions

Conditions	Yield
In chloroform	100%

: 49834-25-5
3,4,5-trimethoxy(N-tert-butylcarbamoyl)benzene

: potassium chloride

: 1600-27-7
mercury(II) diacetate

: (Cl)Hg(C6H(OCH3)3C(O)NHC(CH3)3)

Conditions

Conditions	Yield
With HOAc In ethanol; water air and moisture free atmosphere; refluxing (5 h), stirring (overnight),KCl soln. (H2O) addn., stirring (10 min); filtering, washing (H2O), drying (70°C); elem. anal.;	100%

...Expand

: 1600-27-7
mercury(II) diacetate

: 147-85-3
L-proline

: C10H16HgN2O4

Conditions

Conditions	Yield
With triethylamine In methanol for 0.75h;	100%

: N-(3,5-bis{[ethyl(methyl)amino]methyl}phenyl)hexadecanamide

: 1600-27-7
mercury(II) diacetate

: lithium chloride

: C30H54ClHgN3O

Conditions

Conditions	Yield
Stage #1: N-(3,5-bis{[ethyl(methyl)amino]methyl}phenyl)hexadecanamide; mercury(II) diacetate In ethanol for 24h; Inert atmosphere; Reflux; Stage #2: lithium chloride In ethanol for 0.25h; Inert atmosphere; Reflux;	100%

...Expand

: C37H56N6O7Si

: 1600-27-7
mercury(II) diacetate

: 64-19-7
acetic acid

: (S)-3-(((R)-1-((S)-2-acetamidopropanamido)-4-((diaminomethylene)amino)butyl)dihydroxysilyl)-N,2-dimethylpropanamide acetate

Conditions

Conditions	Yield
Stage #1: C37H56N6O7Si; acetic acid In dichloromethane at 20℃; for 6h; Stage #2: mercury(II) diacetate In dichloromethane at 0℃; for 2h;	100%

...Expand

: 1600-27-7
mercury(II) diacetate

: 4-(trimethylammonio)benzene thiolate hexafluorophosphate

: bis((4-trimethylammonio)benzenethiolate)mercury(II) hexafluorophosphate

Conditions

Conditions	Yield
In methanol; acetonitrile byproducts: acetic acid; soln. of Hg salt in MeOH added to soln. of ligand (2 equiv.) in MeCN; heated to 70°C; stirred for 1 h; cooled to ambient temp.; Et2O layered onto filtrate; crystd. for several d; collected by filtration; washed with Et2O; dried in vac.; elem. anal.;	99.4%

: 1600-27-7
mercury(II) diacetate

: 2-methyl-4,4,5,5-tetramethyl-1,3-dioxolanium perchlorate

A: 76-09-5
2,3-dimethyl-2,3-butane diol

B: C2H3ClHgO6

Conditions

Conditions	Yield
In ethanol for 0.166667h; Heating; Yields of byproduct given;	A n/a B 99%

...Expand

: 1600-27-7
mercury(II) diacetate

: 2-methyl-4,4,5,5-tetramethyl-1,3-dioxolanium perchlorate

A: 76-09-5
2,3-dimethyl-2,3-butane diol

B: C4H5ClHg2O8

Conditions

Conditions	Yield
In ethanol for 0.25h; Heating; Yields of byproduct given;	A n/a B 99%

...Expand

: 1600-27-7
mercury(II) diacetate

: Benzyl 5-O-benzoyl-3-C-<(benzoyloxy)methyl>-2,3-dideoxy-1,4-dithio-D-erythro-pentofuranoside

: 1-O-Acetyl 5-O-benzoyl-3-C-<(benzoyloxy)methyl>-2,3-dideoxy-4-thio-D-erythro-pentofuranose

Conditions

Conditions	Yield
In acetic acid for 0.5h; Ambient temperature;	99%

: 54905-13-4
isopropyl aldehyde dithiophenylacetal

: 1600-27-7
mercury(II) diacetate

: 55999-41-2
(1-Acetoxy-isobutyl)-phenyl-sulfid

Conditions

Conditions	Yield
In acetic acid Ambient temperature;	99%

: 98-98-6
2-Picolinic acid

: 1600-27-7
mercury(II) diacetate

: mercuric pyridine-2-carboxylate

Conditions

Conditions	Yield
In methanol mixing MeOH (or EtOH) solns. of stoich. amts. of Hg(OAc)2 and carboxylic acid; elem. anal.;	99%

: 115560-11-7
(η5-pentamethylcyclopentadienyl)(η5-indenyl)ruthenium(II)

: 1600-27-7
mercury(II) diacetate

: [η5-1,2,3-tris(acetoxymercurio)indenyl](η5-pentamethylcyclopentadienyl)ruthenium(II)

Conditions

Conditions	Yield
In diethyl ether; ethanol under N2; mixt. Ru-complex, 3 equiv Hg-compd., EtOH and Et2O stirred (ambient temp., 12 h); evapn. (reduced pressure), washed (hexane), solid dissolved in CH2Cl2, filtered (Celite), evapn. (reduced pressure), elem. anal.;	99%

: 123-91-1
1,4-dioxane

: (R,R)-N,N'-bis(salicylidene)-1,2-cyclohexanediaminocopper(II)

: 1600-27-7
mercury(II) diacetate

: [(R,R)-N,N'-bis-(salicylidene)-1,2-cyclohexanediaminocopper(II)]Hg(OAc)2*3/5C4H8O2

Conditions

Conditions	Yield
In 1,4-dioxane; methanol salen metal complex dissolved in hot 1,4-dioxane; to this soln. added mercury salt dissolved in MeOH with stirring; mixt. heated at 120°Cfor 5 h; cooled; soln. concd.; crystals were obtained; elem. anal.;	99%

...Expand

: 1600-27-7
mercury(II) diacetate

: 71958-91-3
5,5-dimethyl-2-(3-methyl-3-butenyl)-1,3-cyclohexanedione

: 111120-09-3
2-chloromercurymethyl-2,7,7-trimethyl-3,4,5,6,7,8-hexahydro-2H-benzopyran-5-one

Conditions

Yield

With potassium chloride In tetrahydrofuran; water to a soln. of mercuric acetate in THF is added the olefin-compd. at room temp. under stirring for 3-5 h., a soln. of KCl in water is added and the soln. is stirred for 5 min.; the soln. is diluted with water and extracted with CH2Cl2, the extract is dried over anhydrous Na2SO4 and the solvent is evaporated under red. pressure, benzene is added to the residue and then evaporated, crystn. from AcOEt;

99%

: H2(NC4H2C)4(C6H4NHC(O)C6H4CH2CH(CO2H)CH2C6H4C(O)NHC6H4)2

: 1600-27-7
mercury(II) diacetate

: Hg2(NC4H2C)4(C6H4NHC(O)C6H4CH2CH(CO2)CH2C6H4C(O)NHC6H4)2

Conditions

Conditions	Yield
With diisopropylethylamine In chloroform-d1; d(4)-methanol titration of porphyrine by Hg(OAc)2; monitored by UV; solvent evapd., solid dissolved in CH2Cl2, excess of mercury salt removed by filtration through celite, precipitated with pentane; elem. anal.;	99%
In pyridine room temp.; 15 min; monitored by UV; solvent evapd., solid dissolved in CH2Cl2, excess of mercury salt removed by filtration through celite, precipitated with pentane; elem. anal.;	82%

: 1108157-65-8
1-vinyl-4,5,6,7-tetrahydroindole-2-carbonitrile

: 1600-27-7
mercury(II) diacetate

: 1372648-14-0
2-acetoxy-2-(2-cyano-4,5,6,7-tetrahydroindol-1-yl)ethylmercury acetate

Conditions

Conditions	Yield
In acetonitrile by a react. in dry CH3CN at 60°C for 4 h;	99%

: 1372648-02-6
3-vinyl-4,5-dihydro-3H-benzo[e]indole-2-carbaldehyde

: 1600-27-7
mercury(II) diacetate

: 1372648-17-3
C6H4C2H4C4HNCHO2CCH3CH2HgO2CCH3CHO

Conditions

Conditions	Yield
In acetonitrile by a react. in dry CH3CN at 35°C for 2 h;	99%

Mercury acetate Chemical Properties

IUPAC: Diacetyloxymercury
Mercuric acetate (1600-27-7) is also called for AI3-04458 ; Acetic acid, mercuridi- ; Acetic acid, mercury(2+) salt ; Anthracene, 1,4-dihydro-, compd. with mercury diacetate (1:1) ; Bis(acetyloxy)mercury ; CCRIS 7488 ; Caswell No.543A ; Diacetoxymercury ; EINECS 216-491-1 ; EPA Pesticide Chemical Code 052104 ; HSDB 1244 ; Mercuric diacetate ; Mercury acetate ; Mercury acetate (Hg(CH₃CO₂)₂) ; Mercury acetate (Hg(O₂C₂H₃)₂) ; Mercury diacetate ; Mercury(2+) acetate ; Mercury(II) acetate ; Mercuryl acetate ; NSC 215199 ; Acetic acid, mercury(2+) salt and so on.
Molecular Formula: C₄H₆HgO₄
Molecular Weight: 318.68
EINECS: 216-491-1
Melting Point: 179-182 °C(lit.)
Density: 3,29 g/cm³
LogP: ACD/LogP: -0.29
ACD/LogD (pH 5.5): -1.07
ACD/LogD (pH 7.4): -2.86
ACD/BCF (pH 5.5): 1
ACD/BCF (pH 7.4): 1
ACD/KOC (pH 5.5): 2.73
ACD/KOC (pH 7.4): 1
H bond acceptors: 2
H bond donors: 1
Freely Rotating Bonds: 0
Heavy Atom Count: 9
Formal Charge: 0
Complexity: 108
Isotope Atom Count: 0
Defined Atom StereoCenter Count: 0
Undefined Atom StereoCenter Count: 0
Defined Bond StereoCenter Count: 0
Undefined Bond StereoCenter Count: 0
Covalently-Bonded Unit Count: 1
Flash Point: 40 °C
Enthalpy of Vaporization: 23.7 kJ/mol
Boiling Point: 117.1 °C at 760 mmHg
Vapour Pressure: 13.9 mmHg at 25°C
The appearance of Mercuric acetate (1600-27-7) is white or off-white powder.
The molecular structure of Mercuric acetate (1600-27-7) :

Mercury acetate Uses

Mercuric acetate (1600-27-7) is employed as a reagent to generate organomercury compounds from unsaturated organic precursors.

Mercury acetate Toxicity Data With Reference

1.	oth-mus:oth 50 mg/L	MUREAV Mutation Research. 17 (1973),93.
2.	orl-rat LD50:40,900 µg/kg	GISAAA Gigiena i Sanitariya. 46 (8)(1981),12.
3.	skn-rat LD50:570 mg/kg	GTPZAB Gigiena Truda i Professionalnye Zabolevaniia. Labor Hygiene and Occupational Diseases. 25 (7)(1981),27.
4.	orl-mus LD50:23,900 µg/kg	GISAAA Gigiena i Sanitariya. 46 (8)(1981),12.
5.	ipr-mus LD50:6500 µg/kg	GTPZAB Gigiena Truda i Professionalnye Zabolevaniia. Labor Hygiene and Occupational Diseases. 25 (7)(1981),27.
6.	scu-mus LDLo:20 mg/kg	MOLAAF Monatsschrift fuer Ohrenheilkunde und Laryngo-rhinologie. 73 (1939),751.
7.	ivn-mus LD50:4390 µg/kg	NYKZAU Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. 57 (1961),219.
8.	orl-uns LD50:65 mg/kg	GISAAA Gigiena i Sanitariya. 49 (9)(1984),11.

Mercury acetate Consensus Reports

EPA Extremely Hazardous Substances List. Mercury and its compounds are on the Community Right-To-Know List. EPA Genetic Toxicology Program. Reported in EPA TSCA Inventory.

Mercury acetate Safety Profile

Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Moderately toxic by skin contact. An experimental teratogen. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of Hg. See also MERCURY COMPOUNDS, INORGANIC; MERCURY COMPOUNDS, ORGANIC.
Hazard Codes: T+ Very ,N Dangerous
Risk Statements: 26/27/28-33-50/53
R26/27/28:Very toxic by inhalation, in contact with skin and if swallowed.
R33:Danger of cumulative effects.
R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Safety Statements: 13-28-36-45-60-61
S13:Keep away from food, drink and animal foodstuffs.
S28:After contact with skin, wash immediately with plenty of soap-suds.
S36:Wear suitable protective clothing.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S60:This material and its container must be disposed of as hazardous waste.
S61:Avoid release to the environment. Refer to special instructions / safety data sheets.
RIDADR: UN 1629 6.1/PG 2
WGK Germany: 3
RTECS: AI8575000
TSCA: Yes
HazardClass: 6.1
PackingGroup: II

Mercury acetate Standards and Recommendations

OSHA PEL: CL 0.1 mg(Hg)/m³ (skin)
ACGIH TLV: TWA 0.1 mg(Hg)/m³ (skin); BEI: 35 µg/g creatinine total inorganic mercury in urine preshift; 15 µg/g creatinine total inorganic mercury in blood at end of shift at end of workweek.
DFG MAK: Confirmed Animal Carcinogen with Unknown Relevance to Humans
NIOSH REL: (Mercury, Aryl and Inorganic) CL 0.1 mg/m³ (skin)
DOT Classification: 6.1; Label: Poison

Mercury acetate Specification

1.Reactivity Profile
Mercuric acetate (1600-27-7) is incompatible with acetylene, ammonia, chlorine dioxide, azides, calcium (amalgam formation), sodium carbide, lithium, rubidium, and copper .

Product Name

MERCURIC ACETATE

Synthetic route

Mercury acetate Chemical Properties

Mercury acetate Uses

Mercury acetate Toxicity Data With Reference

Mercury acetate Consensus Reports

Mercury acetate Safety Profile

Mercury acetate Standards and Recommendations

Mercury acetate Specification

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