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Merck
CN

83358

Mercury(II) cyanide

purum p.a., ≥98.0% (precipitation titration)

Synonym(s):

Mercuric cyanide

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About This Item

Linear Formula:
Hg(CN)2
CAS Number:
Molecular Weight:
252.62
EC Number:
209-741-6
UNSPSC Code:
12352302
PubChem Substance ID:
Beilstein/REAXYS Number:
4652800
MDL number:
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InChI key

FQGYCXFLEQVDJQ-UHFFFAOYSA-N

InChI

1S/2CN.Hg/c2*1-2;

SMILES string

N#C[Hg]C#N

grade

purum p.a.

assay

≥98.0% (precipitation titration)

density

3.996 g/mL at 25 °C (lit.)

cation traces

Cd: ≤50 mg/kg, Cu: ≤50 mg/kg, Fe: ≤50 mg/kg, Pb: ≤50 mg/kg, Zn: ≤50 mg/kg

Disclaimer

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

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Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

supp_hazards

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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[Massive penicillin therapy in single series preceded by 3 injections of mercuric cyanide in primary & secondary syphilis; status of the statistics after maximum regression of 9 1/2 years].
M BOLGERT et al.
Bulletin de la Societe francaise de dermatologie et de syphiligraphie, 64(1), 31-39 (1957-01-01)
[Treatment of primary & secondary syphilis by penicillin & mercuric cyanide].
P LECHELLE
Bulletins et memoires de la Societe medicale des hopitaux de Paris, 73(22-24), 698-701 (1957-06-12)
The determination of mercury oxycyanide.
F P WILSON et al.
The Journal of pharmacy and pharmacology, 10(7), 442-446 (1958-07-01)
D Loew et al.
Fortschritte der Medizin, 102(12), 352-354 (1984-03-29)
Heavy metals, including mercury, have recently been in discussion in connection with ecology and therapy. As Meditonsin represents a 0,004% solution of mercury cyanide the following were investigated: absorption, excretion, effect on the kidneys and the chemical behaviour of mercury
R W Myers et al.
Carbohydrate research, 132(1), 61-82 (1984-09-01)
The synthesis and characterization of the anomeric pairs of the per-O-acetylaldohexopyranosyl cyanides of D-galactose, L-fucose, D-glucose, and D-mannose, as well as of 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl cyanide, are described. Cyanation of the readily available, per-O-acetylaldohexopyranosyl bromides with mercuric cyanide in nitromethane, and subsequent

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