64065-U
Ascentis® Express 90 Å Biphenyl (2.7 µm) HPLC Columns
L × I.D. 10 cm × 2.1 mm, HPLC Column
About This Item
Productos recomendados
product name
Ascentis® Express Biphenyl Column, 2.7 μm particle size, L × I.D. 10 cm × 2.1 mm
material
stainless steel hardware
Quality Level
agency
suitable for USP L11
product line
Ascentis®
feature
endcapped
manufacturer/tradename
Ascentis®
packaging
1 ea of
parameter
60 °C max. temp.
9000 psi max. pressure (600 bar)
technique(s)
HPLC: suitable
LC/MS: suitable
UHPLC-MS: suitable
UHPLC: suitable
L × I.D.
10 cm × 2.1 mm
surface area
135 m2/g
impurities
<5 ppm metals
matrix
particle platform (Fused-Core)
superficially porous particle
matrix active group
biphenyl phase
particle size
2.7 μm
pore size
90 Å pore size
operating pH
2-9
application(s)
food and beverages
separation technique
reversed phase
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General description
Legal Information
Guard column
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Artículos
Determination of plasma protein binding using a SupelTM C18 pin device based BioSPME method for efficient sample preparation, along with a comparison to the equilibrium dialysis method.
The application note describes a comparative analysis of plasma protein binding results for free/bound drugs using two different sample extraction steps, with and without agitation.
Learn about Supel™ BioSPME C18 high-throughput devices to determine plasma protein binding and decrease the sample preparation time to less than an hour.
Comparative analysis of Supel™ BioSPME 96-Pin device with a rapid equilibrium dialysis technique for accuracy of measured values, sample cleanliness, and workflow time in drug protein binding.
Protocolos
HPLC-UV analysis of active compounds in marijuana-infused edibles for potency testing; complex matrix requires precise methods.
Rapid potency testing of marijuana-infused edibles using LC/MS on a biphenyl stationary phase detected eleven cannabinoids.
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