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544973

Sigma-Aldrich

Ytterbium(III) acetate hydrate

99.95% trace metals basis

Synonym(s):

Acetic acid ytterbium hydrate

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About This Item

Linear Formula:
Yb(C2H3O2)3 · xH2O
Molecular Weight:
350.17 (anhydrous basis)
EC Number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

99.95% trace metals basis

form

powder or crystals

reaction suitability

core: ytterbium
reagent type: catalyst

SMILES string

O.CC(=O)O[Yb](OC(C)=O)OC(C)=O

InChI

1S/3C2H4O2.H2O.Yb/c3*1-2(3)4;;/h3*1H3,(H,3,4);1H2;/q;;;;+3/p-3

InChI key

PHWPQNTXTCAARQ-UHFFFAOYSA-K

Application

  • Highly luminescent, biocompatible ytterbium (III) complexes as near-infrared fluorophores for living cell imaging: This study highlights the development of ytterbium complexes with enhanced near-infrared luminescence suitable for live-cell imaging, utilizing Ytterbium(III) acetate hydrate as a precursor. The findings demonstrate significant potential for biomedical applications, particularly in imaging techniques sensitive to deeper tissue penetration (Ning et al., 2018).

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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In this work, we developed a simple and selective luminescence sensing system for detecting ascorbic acid (AA) based on NaGdF4:Yb,Er@NaYF4 upconversion nanoparticles (UCNPs) and oxidase-like CoOOH nanoflakes. When p-phenylenediamine (PPD) and oxidase-like CoOOH nanoflakes were added to the UCNPs solutions
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This paper presents the use of soft template method to synthesize core and core-shell up-converting nanoparticles usefull for temperature sensing applications. Based on the stock solutions of core β-NaYF4:Er3+,Yb3+ nanoparticles and involving soft template method without any additional process of
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Lanthanide-doped upconversion nanoparticles with a suitable surface coating are appealing for biomedical applications. Because high-quality upconversion nanoparticles are typically prepared in an organic solvent and passivated by hydrophobic oleate ligands, a convenient and reliable method for the surface modification of

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