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Safety Information

60759

Supelco

Silica gel C₈-Reversed phase Inorganic Sorbent

230-400 mesh, fully endcapped

Synonym(s):

Reversed phase silica gel C8

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About This Item

EC Number:
231-545-4
MDL number:
MFCD00148339
UNSPSC Code:
12000000
NACRES:
SB.52

product name

Silica gel C8-Reversed phase, for column chromatography, fully endcapped

grade

for column chromatography

Quality Level

100

form

powder

quality

fully endcapped

technique(s)

LPLC: suitable

matrix

Silica

matrix active group

C8

particle size

40-63 μm

pore size

90 Å pore size

separation technique

reversed phase

General description

Reversed-phase silica gels are generally suitable to retain catalysts by hydrophobic interactions.

Application

Silica gel C8-reversed phase was used in the purification of tertiary sulphonamide using FSPE. Pressure induced C8 reversed phase silica gel was synthesized through a sol-gel templating technique.

Storage Class Code

11 - 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.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

60759-VAR:
60759-BULK:
60759-50G:
60759-250G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW4626
BCBV1617
BCBR7488V
BCBP4025V
BCBH0286V

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Effective viscosity of glycerin in a nanoporous silica gel.
Han, Aijie, et al.
Journal of Applied Physics, 104, 124904-124904 (2008)
J Horn et al.
Topics in current chemistry, 242, 43-75 (2004-01-01)
Catalysts immobilized on solid supports have become valuable tools for simplified product isolation and catalyst recycling. An alternative to covalent attachment to a solid support is to immobilize catalysts by non-covalent bonding through hydrogen bridges, or ionic, hydrophobic or fluorous
Fluorous scavenger for parallel preparation of tertiary sulfonamides leading to secondary amines.
Basle, Emmanuel, et al.
Tetrahedron Letters, 48, 8138-8140 (2007)

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