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Ammonium tetrathiomolybdate

ALDRICH/323446 - 99.97% trace metals basis

Synonym: Ammonium thiomolybdate; Diammonium tetrathiomolybdate

CAS Number: 15060-55-6
Empirical Formula (Hill Notation): H8MoN2S4
Molecular Weight: 260.28
MDL Number: MFCD00136013
Linear Formula: (NH4)2MoS4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-323446-1G 1 g
 $50.30
1/EA		 Add To Favorites
45-323446-10G 10 g
 $257.00
1/EA		 Add To Favorites
45-323446-50G 50 g
 $921.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 323446-50G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 323446-10G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 323446-1G

 

assay 99.97% trace metals basis
form crystalline
impurities ≤350.0 ppm Trace Metal Analysis
InChI 1S/Mo.2H3N.4S/h;2*1H3;;;;/q;;;;;2*-1/p+2
InChI key PQNOIAHNKHBLRN-UHFFFAOYSA-P
mp >300 °C (lit.)
Quality Level 100 
reaction suitability reagent type: catalyst
SMILES string [NH4+].[NH4+].[S-][Mo]([S-])(=S)=S
Application: Ring opening of aziridines leading to sulfides and disulfides.
Application: This classic building block for transition metal sulfide cluster compounds was recently used in a low-temperature, solid state synthesis of a new series of heterometallic sulfide clusters stabilized with dppm [bis(diphenylphosphino)methane] ligands.
Biochem/physiol Actions: Acts as a chelator in vivo to reduce copper levels. Tetrathiomolybdate interferes with angiogenesis and reduces tumor growth. Its mechanism may involve inhibition of NF-κB and downstream cytokines.
Packaging: 1, 10, 50 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity 99.97% trace metals basis
mp >300 °C (lit.)
UNSPSC 12352302

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