SIL350
Silicic acid
BioReagent, suitable for column chromatography, 100-200 mesh (75 - 150 μm)
Synonym(s):
hydrated silica, metasilcic, silica acid
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All Photos(3)
About This Item
Empirical Formula (Hill Notation):
H2O3Si
CAS Number:
Molecular Weight:
78.10
EC Number:
MDL number:
UNSPSC Code:
23201100
PubChem Substance ID:
NACRES:
SB.54
Recommended Products
product line
BioReagent
Quality Level
Assay
≥99.8% Si (as SiO2) basis
form
solid
particle size
100-200 mesh (75 - 150 μm)
suitability
suitable for column chromatography
SMILES string
O[Si](O)=O
InChI
1S/H2O3Si/c1-4(2)3/h1-2H
InChI key
IJKVHSBPTUYDLN-UHFFFAOYSA-N
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Application
For general chromatographic use.
Silicic acid has been used as a column material for the purification of polyunsaturated fatty acids, fatty acid methyl ester, nucleic acid extraction from Suillus bovinus and lipid fractionation from soy milk powder.
Silicic acid is used in protein chromatography. Silicic acid has been used in a study to demonstrate the anti-biofilm potential of a glycolipid surfactant produced by a tropical marine strain of Serratia marcescens. Silicic acid has also been used to study the antioxidant activity of fresh and processed Jalapeño and Serrano peppers.
Biochem/physiol Actions
Silicic acid polymers are employed in water treatment systems, drug encapsulation cum delivery and for soluble nanoparticle generation. Silicic acid interacts with aluminum and reduces its bioavailability. It is an effective antidote for aluminum poisoning.
Preparation Note
Acid-washed.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Silicic acid: its gastrointestinal uptake and urinary excretion in man and effects on aluminium excretion
Reffitt DM, et al.
Journal of Inorganic Biochemistry, 76(2), 141-147 (1999)
<I>Suillus bovinus</I> glutamine synthetase gene organization, transcription and enzyme activities in the Scots pine mycorrhizosphere developed on forest humus.
Juuti, J.T., et al.
The New phytologist, 164(2), 389-399 (2004)
Leroy S Pakkiri et al.
Glycobiology, 15(3), 291-302 (2004-10-16)
Based on recent analytical and enzymological studies, a topological model for the role of alpha-D-mannosyl-(1-->3)-alpha-D-mannosyl-(1-->3)-diacylglycerol (Man(2)-DAG) as a lipid anchor precursor and mannosylphosphorylundecaprenol (Man-P-Und) as a mannosyl donor in the assembly of a membrane-associated lipomannan (LM) in Micrococcus luteus has
Koki Nagayama et al.
The Journal of antimicrobial chemotherapy, 50(6), 889-893 (2002-12-04)
The bactericidal activity of phlorotannins from brown algae against food-borne pathogenic bacteria (25 strains), methicillin-resistant Staphylococcus aureus (MRSA) (nine strains) and Streptococcus pyogenes (one strain) was examined and compared with that of catechins. In addition, the effect of the oral
Silicic acid condensation under the influence of water-soluble polymers: from biology to new materials
Annenkov VV, et al.
Royal Society of Chemistry Advances, 7(34), 20995-21027 (2017)
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