480746
Bismuth(III) citrate
99.99% trace metals basis, −325 mesh
Synonym(s):
Bismuth citrate
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About This Item
Linear Formula:
[O2CCH2C(OH)(CO2)CH2CO2]Bi
CAS Number:
Molecular Weight:
398.08
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99.99% trace metals basis
reaction suitability
core: bismuth
reagent type: catalyst
particle size
−325 mesh
mp
300 °C (dec.) (lit.)
density
0.94 g/mL at 25 °C (lit.)
SMILES string
OC12CC(=O)O[Bi](OC(=O)C1)OC2=O
InChI
1S/C6H8O7.Bi/c7-3(8)1-6(13,5(11)12)2-4(9)10;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);/q;+3/p-3
InChI key
ANERHPOLUMFRDC-UHFFFAOYSA-K
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General description
Bismuth(III)citrate is a main-group metal complex of bismuth(III) with three citrateligands. The complex has been used as a bismuth (III) source for Bi(III)radiolabeled compounds.
Application
Bismuth(III) citrate has been used as a sorbent in spin columns to develop a novel stationary phase for the selective and efficient isolation of phenolic compounds from natural sources via solid phase extraction (SPE) method. It can be used to synthesize bismuth subcarbonate ((BiO)2CO3) nanotubes that are reported to show antibacterial property against Helicobacter pylori.
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
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Christos Kokkinos et al.
Analytica chimica acta, 886, 29-36 (2015-09-01)
A novel immunosensor based on graphite screen-printed electrodes (SPEs) modified with bismuth citrate was developed for the voltammetric determination of C-reactive protein (CRP) in human serum using quantum dots (QDs) labels. The sandwich-type immunoassay involved physisorption of CRP capture antibody
Rong Chen et al.
Chemical communications (Cambridge, England), (21)(21), 2265-2267 (2006-05-24)
Bismuth subcarbonate ((BiO)2CO3) nanotubes with uniform diameters of about 3-5 nm were fabricated from bismuth citrate; these nanotubes exhibit antibacterial properties against Helicobacter pylori (50% inhibition at 10 microg mL(-1)), a bacterium causing peptic ulcers and gastritis.
Carlos Ayala-Torres et al.
Microbiological research, 176, 1-6 (2015-06-14)
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Shah Hussain et al.
Journal of pharmaceutical and biomedical analysis, 84, 148-158 (2013-07-09)
Galloyl- and caffeoylquinic acids are among the most important pharmacological active groups of natural compounds. This study describes a pre-step in isolation of some selected representatives of these groups from biological samples. A selective solid-phase extraction (SPE) method for these
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