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35483

Supelco

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:
1343-88-0
Molecular Weight:
100.39
EC Number:
215-681-1
MDL number:
MFCD00078249
UNSPSC Code:
23201100
PubChem Substance ID:
57649396

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

35483-100G:
35483-1KG:

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Certificates of Analysis (COA)

Lot/Batch Number
SZBF2260V
SZBE3570V
SZBF0710V
91830
32740

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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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