Waters, 186003568, XBridge Peptide BEH C18 Column, 130Å, 3.5 µm, 4.6 mm X 100 mm, 1K - 15K, 1/pk

The XBridge BEH130 C18 Peptide Separation Technology (PST) columns are optimized and QC tested for peptide separations. The small-pore (130Å) trifunctionally bonded BEH particle offers you the widest usable pH range, superior low pH stability, and ultra-low column bleed to assay samples for proteomics, protein characterization, and peptide synthesis.

Specifications
Chemistry: C18
Separation Mode: Reversed Phase
Particle Substrate: Hybrid
pH Range Min: 1 pH
pH Range Max: 12 pH
Maximum Pressure: 6000 psi (415 Bar)
Endcapped: Yes
Silanol Activity: Low
Molecular Weight Range Min: 1000
Molecular Weight Range Max: 15000
Particle Shape: Spherical
Particle Size: 3.5 µm
Endfitting Type: Waters
Pore Size: 130 Å
QC Tested: Peptide
Format: Column
Surface Area: 185
System: HPLC
Particle Technology: BEH
USP Classification: L1
Inner Diameter: 4.6 mm
Length: 100 mm
Carbon Load: 17 %
UNSPSC: 41115709
Application: Peptide
Brand: XBridge
Product Type: Columns
Units per Package: 1 pk

Additional Information
XBridge Peptide BEH C18 Column, 130Å, 3.5 µm, 4.6 mm X 100 mm, 1K - 15K, 1/pk The small-pore (130) tri-functionally bonded BEH particle offers you the widest usable pH range, superior low pH stability, and ultra-low column bleed to assay samples for proteomics, protein characterization, and peptide synthesis, so add the XBridge Peptide BEH C18 Column to your lab equipment collection. Waters Peptide Separation Technology (PST) was used to optimize the column, and it was QC tested for peptide separations. Synthetic particles provide the highest level of quality and consistency in performance. You can rely on the analytical column's consistency to achieve consistent synthetic peptide and protein digest separations from batch to batch. The XBridge Peptide BEH C18 Column is QC verified with a peptide map to ensure the stability of peptide separation processes. This is made achievable by using well-characterized, cutting-edge C18 ligand bonding techniques. It performs consistently with a wide range of samples used in proteomics, protein characterization, and peptide synthesis. The XBridge Peptide BEH C18 Column is created with procedures that ensure stable particle structure and bonding chemistry at increased temperatures and pH levels ranging from 1 to 12. The XBridge Peptide BEH C18 Columns are exceptionally dependable, providing excellent quality and consistent results. These Columns are manufactured in dedicated Waters manufacturing plants and facilities that adhere to the most stringent cGMP and ISO 9001 standards, giving you peace of mind when using your equipment and knowing you can trust the results. The XBridge Peptide BEH C18 Columns' packing materials have been designed to provide excellent peak shape, high efficiency, and outstanding stability. The XBridge Peptide BEH C18 Column's unique properties allow for batch-to-batch consistency in synthetic peptide and protein digest separations. The C18 ligand in the XBridge Peptide BEH C18 Column helps to provide a stable, well-characterized baseline for various proteomics, peptide synthesis, and protein characterization samples. You can browse through our website to shop for lab equipment, as well as to reach out with any queries you may have to a member of our global support team. You may also want to review the XBridge BEH C18 VanGuard Cartridge, 130Å, 5 µm, 2.1 mm X 5 mm, 3/pk; as this XBridge BEH C18 VanGuard Cartridge is used to extend analytical column lifetime and performance by removing particulate contamination from the mobile phase stream. This cartridge is optimized to protect all 2.1 mm and 3.0 mm I.D. XBridge BEH C18 analytical columns containing 5 µm sorbent particles.

FAQ
What Is Mass Spectrometry's Principle in Chromatography? The basic idea behind mass spectrometry (MS) is to produce ions from inorganic or organic substances using any suitable method, then separate them by their mass to charge ratio (m/z) and detect them qualitatively and quantitatively based on their m/z and abundance.