228672
Samarium(III) oxide
99.9% trace metals basis
Sinónimos:
Samaria
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About This Item
Productos recomendados
Quality Level
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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Categorías relacionadas
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Treatment of systemic disease with phosphorothioate antisense oligonucleotides (PS ASOs) has been accomplished using local or parenteral routes of administration to date. This report describes, for the first time, the effective oral delivery of a second generation oligonucleotide where significant
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 8(3), 193-201 (1999-06-24)
The effect of the neutron activation factors, i.e., admixture of samarium oxide (Sm2O3) and irradiation time, on the physico-chemical properties of the raw materials and the in vitro dissolution and disintegration of hydrophilic and lipophilic suppositories was investigated. It was
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
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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