35483
Florisil®
suitable for thin layer chromatography (TLC)
Sinonimo/i:
Magnesio silicato, Magnesio silicato attivato
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About This Item
Formula empirica (notazione di Hill):
MgO3Si
Numero CAS:
Peso molecolare:
100.39
Numero CE:
Numero MDL:
Codice UNSPSC:
23201100
ID PubChem:
Prodotti consigliati
tecniche
LPLC: suitable
thin layer chromatography (TLC): suitable
Stringa SMILE
[Mg++].[O-][Si]([O-])=O
InChI
1S/Mg.O3Si/c;1-4(2)3/q+2;-2
FKHIFSZMMVMEQY-UHFFFAOYSA-N
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Descrizione generale
Florisil, adsorbent for the separation of lipids is a commercially-prepared magnesia silica gel. It has a coarse mesh size which helps in rapid flow rate. Florisil is effective in promoting [1,3]-sigmatropic shift of myceophenolic acid related allyl phenyl ethers. Florisil cartridges are used in atmospheric sampling to assess possible interference from air contaminants.
Applicazioni
Florisil® TLC was used in TLC separations of organic compounds.
Note legali
Florisil is a registered trademark of U.S. Silica Company
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
nwg
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Retention behaviour of model solutes on mixed silica-magnesia adsorbents by TLC. Comparison with the adsorption properties of Florisil.
Waksmundzka-Hajnos,
Chromatographia, 43, 405-412 (1996)
P A de Paula Pereira et al.
Talanta, 49(2), 245-252 (2008-10-31)
A new sampling protocol was developed to determine methanol and ethanol in the gas phase, at low concentration levels, in urban atmospheres. The procedure involves collection of air samples (20.0-30.0 l) with three florisil cartridges connected in series, at a
The Florisil? catalyzed [1, 3]-sigmatropic shift of allyl phenyl ethers-An entryway into novel mycophenolic acid analogues.
Talamas, Francisco X., et al.
Tetrahedron Letters, 38, 4725-4728 (1997)
Acid-treated Florisil as an adsorbent for column chromatography
Carroll, K. K.
Journal of the American Oil Chemists' Society, 40, 413-419 (1963)
U Avsar et al.
Cellular and molecular biology (Noisy-le-Grand, France), 59 Suppl, OL1835-OL1841 (2013-02-13)
This study evaluated the protective effect of Panax Ginseng (PG) on bone metabolism in an experimental ovariectomy (OVX) model of osteoporosis in which inflammation was induced by subcutaneous magnesium silicate. The groups were: sham control (Group1, SH), sham+inflammation (Group2, SHinf)
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