35483
Florisil® TLC
suitable for thin layer chromatography (TLC)
Synonym(s):
Florisil®, Activated magnesium silicate, Magnesium silicate
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About This Item
Empirical Formula (Hill Notation):
MgO3Si
CAS Number:
Molecular Weight:
100.39
EC Number:
MDL number:
UNSPSC Code:
23201100
PubChem Substance ID:
Recommended Products
technique(s)
LPLC: suitable
thin layer chromatography (TLC): suitable
SMILES string
[Mg++].[O-][Si]([O-])=O
InChI
1S/Mg.O3Si/c;1-4(2)3/q+2;-2
InChI key
FKHIFSZMMVMEQY-UHFFFAOYSA-N
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General description
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.
Application
Florisil® TLC was used in TLC separations of organic compounds.
Legal Information
Florisil is a registered trademark of U.S. Silica Company
Storage Class Code
13 - Non Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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