The reproducibility of a chromatographic column has a critical impact on the long-term reliability and robustness of an analytical method, and its reproducibility lies completely outside the user’s control. With exceptional batch-to-batch and column-to-column reproducibility, Waters well-established particle and column manufacturing process control provides confidence in the long-term reliability of your analytical method. ACQUITY OST C18, 135A, 1.7um Method Validation Kit includes three batches of chromatographic media [derived from different base particles] to judge the quality, reliability, and consistency of your chromatographic method. Each batch of selected ACQUITY OST C18, 135A, 1.7um chemistry is specifically QC tested with a mixture of synthetic oligonucleotides to help ensure consistent performance.
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Chemistry
C18
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Separation Mode
Reversed Phase
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Particle Substrate
Hybrid
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pH Range Min
1 pH
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pH Range Max
12 pH
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Endcapped
Yes
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Silanol Activity
Low
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Molecular Weight Range Min
1000
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Molecular Weight Range Max
30000
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Particle Shape
Spherical
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Particle Size
1.7 µm
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Endfitting Type
Parker-style
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Pore Size
130 Å
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QC Tested
Oligonucleotide
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Format
Method Validation Kit
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Surface Area
185
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System
UPLC, UHPLC
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Particle Technology
BEH
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USP Classification
L1
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Inner Diameter
2.1 mm
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Length
100 mm
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Carbon Load
18 %
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UNSPSC
41115709
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Application
Oligonucleotide, Gene Therapeutics
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Brand
ACQUITY UPLC
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Product Type
Column Kits
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Units per Package
3 pk