SKU: 186003334
XBridge BEH Phenyl Column, 130Å, 3.5 µm, 4.6 mm X 100 mm, 1/pk

XBridge BEH Phenyl Columns | 186003334


Streamline Purchasing with Customized Quotes

Streamline Purchasing with Customized Quotes

Shop on Waters.com and add items to your cart

Navigate to the Shopping Cart

Select Request a Quote to get your quote instantly


Product Description

XBridge BEH Phenyl columns provide complementary selectivity to C18 stationary phases, especially for polyaromatic compounds. This most chemically stable commercially available Phenyl sorbent on the market and provides you with ultra-low column bleed, long column lifetimes and excellent peak shape.

Specifications

  • Chemistry

    Phenyl

  • 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

  • Bonding Technology

    Phenyl-Hexyl

  • Silanol Activity

    Low

  • Particle Shape

    Spherical

  • Particle Size

    3.5 µm

  • Endfitting Type

    Waters

  • Pore Size

    130 Å

  • Format

    Column

  • Surface Area

    185

  • System

    HPLC

  • Particle Technology

    BEH

  • USP Classification

    L11

  • Inner Diameter

    4.6 mm

  • Length

    100 mm

  • Carbon Load

    15 %

  • UNSPSC

    41115709

  • Brand

    XBridge

  • Product Type

    Columns

  • Units per Package

    1 pk

Product Support

Documents

Documents



What do you want to do?

What do you want to do?

Related Products

Back To Top Back To Top

XBridge BEH Phenyl Column, 130Å, 3.5 µm, 4.6 mm X 100 mm, 1/pk

Leverage the unmatched column lifetime of the XBridge BEH Phenyl Column to meet the needs of chromatographic analysis. The lab equipment is unique in that it offers the flexibility to work across a range of mobile phase pH and temperature. You can also seamlessly transfer methods to UPLC technology with the XBridge BEH Phenyl Column.

Depend on the XBridge BEH Phenyl Column with confidence where alternative selectivity is required in separations. It is especially useful for analytes that contain an aromatic ring. Compared to traditional phenyl liquid chromatography columns, the XBridge BEH Phenyl Column offers a wider usable pH range, allowing more robust method development. This is made possible due to the novel bonding and end-capping of the BEH particle technology on which the XBridge BEH Phenyl Column is based. The trifunctional bonding of the phenyl hexyl-ligand enables the analytical column to offer exceptional low and high pH stability, which in turn makes it the most reproducible phenyl column in the market.

Compared to straight-chain-alkyl columns and embedded-polar-group columns, the XBridge BEH Phenyl Column provides alternate selectivity for compounds containing an aromatic moiety. This results in higher flexibility in developing orthogonal methods for particularly challenging separations.

Shop for lab equipment, and check all related products and other variants of the same listing through our website. You can also explore our complete range of products and brands while reading more about the methods used in the development of our equipment.

You may also be interested in XBridge BEH Phenyl-Hexyl VanGuard Cartridge, 130Å, 3.5 µm, 3.9 mm X 5 mm, 3/pk which is the ideal lab equipment to extend the lifetime of your analytical column. Manufactured from the same packing materials as the column, the cartridge works by removing all chemical and particulate contamination from the mobile phase, thus not only protecting your column but also ensuring that your analysis yields reliable results every time.

What Are Aromatic Rings?

Aromatic rings (also known as aromatic compounds or arenes) are hydrocarbons that contain benzene, or some other related ring structure. Benzene, C6H6, is often drawn as a ring of six carbon atoms, with alternating double bonds and single bonds. As a general rule, aromatic hydrocarbons are nonpolar and are insoluble in water. However, they may be very water-soluble when other atoms are substituted on the benzene ring.