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Sigma-Aldrich

Magnesia grooves

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About This Item

Empirical Formula (Hill Notation):
MgO
Molecular Weight:
40.30
EC Number:
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:

reaction suitability

reagent type: catalyst
core: magnesium

SMILES string

O=[Mg]

InChI

1S/Mg.O

InChI key

CPLXHLVBOLITMK-UHFFFAOYSA-N

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Packaging

package of 100 pieces

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Solaiman Tarafder et al.
Journal of biomedical materials research. Part B, Applied biomaterials, 103(3), 679-690 (2014-07-22)
The presence of interconnected macro pores allows guided tissue regeneration in tissue engineering scaffolds. However, highly porous scaffolds suffer from having poor mechanical strength. Previously, we showed that microwave sintering could successfully be used to improve mechanical strength of macro
Lin Zhong et al.
Drug development and industrial pharmacy, 40(12), 1660-1669 (2013-10-09)
The amorphous solid dispersions of telmisartan salts were prepared by cogrinding, in presence of alkalizers and polyvinylpyrrolidone (PVPk30). Five alkalizers in this study were MgO, Na2CO3, K2CO3, NaHCO3 and meglumine. In soft mode using a roll mill, the drug could
Tobias C Keller et al.
ChemSusChem, 7(6), 1729-1738 (2014-04-24)
High-silica zeolites have been reported recently as efficient catalysts for liquid- and gas-phase condensation reactions because of the presence of a complementary source of basicity compared to Al-rich basic zeolites. Herein, we describe the controlled generation of these active sites
Kazuhiro Iguchi et al.
Oncology letters, 7(5), 1665-1668 (2014-04-26)
Prostate cancer occurs more frequently among older males and such elderly individuals often have chronic underlying disorders for which various drugs are administered for treatment. The levels of prostate-specific antigen (PSA), a widely used prostate cancer marker, are influenced by
Ayuko Imaoka et al.
Drug metabolism and pharmacokinetics, 29(5), 414-418 (2014-05-09)
The drug interaction between new quinolone antibiotics (NQs) and polyvalent metal cation products, leading to a significant decrease in the absorption of NQ, is considered to be attributable to the formation of poorly absorbable chelate and physicochemical adsorption of NQs

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