Silver sulfide

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Names

[ CAS No. ]:
21548-73-2

[ Name ]:
Silver sulfide

[Synonym ]:
Silver(1+) sulfidosilver
MFCD00003406
EINECS 244-438-2
Disilver(1+) sulfide

Chemical & Physical Properties

[ Density]:
7.234 g/mL at 25 °C(lit.)

[ Melting Point ]:
845 °C(lit.)

[ Molecular Formula ]:
Ag2S

[ Molecular Weight ]:
247.801

[ Exact Mass ]:
245.782257

[ PSA ]:
25.30000

[ LogP ]:
0.64820

[ Stability ]:
Stable. Incompatible with acids, strong oxidizing agents.

MSDS

Safety Information

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Aqueous synthesis of highly luminescent AgInS₂-ZnS quantum dots and their biological applications.

Nanoscale 5(6) , 2322-7, (2013)

Highly emissive and air-stable AgInS2-ZnS quantum dots (ZAIS QDs) with quantum yields of up to 20% have been successfully synthesized directly in aqueous media in the presence of polyacrylic acid (PAA...

Ag2S-ZnO--an efficient photocatalyst for the mineralization of Acid Black 1 with UV light.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 105 , 314-9, (2013)

The Ag(2)S loaded ZnO (Ag(2)S-ZnO) was successfully synthesized by precipitation of zinc oxalate and Ag(2)S and calcination of the mixed precipitate at 400 °C for 12 h. The catalyst was characterized ...

Highly efficient antiviral and antibacterial activities of solid-state cuprous compounds.

J. Hazard. Mater. 235-236 , 265-70, (2012)

We found that several solid-state cuprous compounds, including cuprous oxide (Cu(2)O), sulfide (Cu(2)S), iodide (CuI), and chloride (CuCl), have highly efficient antiviral activities, whereas those of...


More Articles


Related Compounds

  • Gold silver sulfide
  • Copper silver sulfide
  • copper silver sulfide
  • BISMUTH SILVER SULFIDE
  • Gallium silver sulfide
  • Niobium silver sulfide
  • 1-(4-((4-Fluorophenyl)sulfonyl)piperidin-1-yl)-2-(thiophen-2-yl)ethanone
  • 2-(Benzylthio)-1-(4-((4-fluorophenyl)sulfonyl)piperidin-1-yl)ethanone
  • (1R,5S)-8-((3,4-difluorophenyl)sulfonyl)-3-(phenylsulfonyl)-8-azabicyclo[3.2.1]octane
  • N-(3-methylisoxazol-5-yl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(5-methyl-1,3,4-thiadiazol-2-yl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(6-ethoxybenzo[d]thiazol-2-yl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(4-(furan-2-yl)thiazol-2-yl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(4-(N-(4-methylpyrimidin-2-yl)sulfamoyl)phenyl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(4-bromo-3-methylphenyl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
  • N-(4-methylbenzo[d]thiazol-2-yl)-6-(1H-1,2,4-triazol-1-yl)pyridazine-3-carboxamide
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