228672
Samarium(III) oxide
99.9% trace metals basis
Synonym(s):
Samaria
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About This Item
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Assay
99.9% trace metals basis
form
powder
reaction suitability
reagent type: catalyst
core: samarium
density
8.35 g/mL at 25 °C (lit.)
SMILES string
O=[Sm]O[Sm]=O
InChI
1S/3O.2Sm
InChI key
PRCWVHVINXAFRG-UHFFFAOYSA-N
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Related Categories
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Pharmaceutical research, 24(4), 695-704 (2007-03-21)
To develop a robust radiolabeling technique to enable evaluation of difficult to radiolabel gastric retentive formulations using gamma scintigraphy. The use of a successful radiolabel will allow accurate assessment of the gastric residence time of the formulations. The retention of
International journal of pharmaceutics, 281(1-2), 3-10 (2004-08-04)
This paper is a report from a pharmacoscintigraphic study with an Egalet constant-release system containing caffeine and natural abundance samarium oxide. First the formulation was tested in vitro to clarify integrity during irradiation in the nuclear reactor. Then six healthy
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(4), 933-939 (2004-03-24)
Microphone based photoacoustic (PA) spectrometer to study solids in powder form was designed and fabricated. Laser PA spectra of Sm3+ ion in Sm2O3 and SmCl3.6H2O microcrystalline powders were recorded first time in 484-542 nm spectral region at room temperature. Analysis
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 67(1), 46-49 (2008-08-19)
Cross sections of the (147)Sm(n, alpha)(144)Nd reaction were measured at En=5.0 and 6.0MeV. A twin gridded ionization chamber was used as a charged particle detector and two large area (147)Sm(2)O(3) samples placed back to back were employed. Experiments were performed
Journal of biomedical materials research. Part A, 94(1), 130-136 (2010-02-04)
The biocompatibility of natural samarium (III) oxide, which has previously been used for treatment in bone-related diseases was determined as a first step in its evaluation as a bone implant material. Assessment for 28 days using osteoblast-like cells revealed no
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