337382
Silver phosphate
98%
Synonym(s):
Silver orthophosphate
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About This Item
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Quality Level
Assay
98%
form
powder
mp
849 °C (lit.)
SMILES string
[Ag+].[Ag+].[Ag+].[O-]P([O-])([O-])=O
InChI
1S/3Ag.H3O4P/c;;;1-5(2,3)4/h;;;(H3,1,2,3,4)/q3*+1;/p-3
InChI key
FJOLTQXXWSRAIX-UHFFFAOYSA-K
Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Rapid communications in mass spectrometry : RCM, 25(5), 579-584 (2011-02-04)
Stable oxygen isotope compositions (δ(18)O values) of two commercial and one synthesized silver orthophosphate reagents have been determined on the VSMOW scale. The analyses were carried out in three different laboratories: lab (1) applying off-line oxygen extraction in the form
Journal of mass spectrometry : JMS, 44(6), 879-890 (2009-01-09)
Oxygen isotope values of biogenic apatite have long demonstrated considerable promise for paleothermometry potential because of the abundance of material in the fossil record and greater resistance of apatite to diagenesis compared to carbonate. Unfortunately, this promise has not been
Journal of the American Chemical Society, 135(4), 1280-1283 (2013-01-11)
We report a Ag(3)PO(4) microparticle system showing collective behaviors in aqueous medium. Transition between two emergent patterns, namely "exclusion" and "schooling", can be triggered by shift in chemical equilibrium upon the addition or removal of NH(3) or in response to
Journal of the American Chemical Society, 134(9), 4096-4099 (2012-02-15)
A kinetic resolution of α-allenic alcohols is realized through chiral silver phosphate-catalyzed cycloisomerization with high stereoselectivity (selectivity factor up to 189) and tolerance of a variety of functional groups. A mechanistic model is proposed to interpret the origin of the
Formal synthesis of (-)-cephalotaxine based on a tandem hydroamination/semipinacol rearrangement reaction.
Chemistry, an Asian journal, 7(5), 894-898 (2012-03-03)
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