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CLEARANCE Waters Tubing Assembly, I-Class CM-A, High Pressure, 0.003 Stainless Steel, 14.5 inches - 700008869
£250.00 £102.50
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Save: 59% off
CLEARANCE Waters XBridge BEH C18 Method Validation Kit, 130 A, 5 um, 4.6 mm ID x 150 mm Length, 3/pk - 186003775
£2,824.00 £1,161.42
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CLEARANCE Agilent Certified Clear Headspace Vials, Crimp, Flat-bottom, 20 mL, 100/Pk - 5182-0837
£48.63 £22.05
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CLEARANCE Glass Expansion Thermo iCAP 6000, Gold - 70-900-4002G, 5000-111
£203.96 £148.00
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CLEARANCE Waters Guard-Pak Holder - WAT088141
£612.00 £381.09
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Save: 38% off
New Products - [more]
VDS optilab PE Tubing, ID x OD: 1.5 mm x 3.0 mm, 5 m/PCK, fluorine-free solvent supply tubing - 222725
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PerkinElmer
| Item Name | Product Image | Price |
|---|---|---|
PerkinElmer Brownlee SPP 2.7 µm PFP 3.0 X 30 mm - N9308471Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 3.0 X 50 mm - N9308472Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 3.0 X 75 mm - N9308473Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 3.0 X 100 mm - N9308474Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 3.0 X 100 mm - N9308475Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 4.6 X 30 mm - N9308476Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 4.6 X 50 mm - N9308477Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 4.6 X 75 mm - N9308478Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 4.6 X 100 mm - N9308479Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm PFP 4.6 X 150 mm - N9308480Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 2.1 X 150 mm - N9308486Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 3.0 X 30 mm - N9308487Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 3.0 X 50 mm - N9308488Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 3.0 X 75 mm - N9308489Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 3.0 X 100 mm - N9308490Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 3.0 X 150 mm - N9308491Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 4.6 X 30 mm - N9308492Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 4.6 X 50 mm - N9308493Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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Live chat below or contact us for latest price. ... more info |
PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 4.6 X 75 mm - N9308494Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
|
Live chat below or contact us for latest price. ... more info |
PerkinElmer Brownlee SPP 2.7 µm Phenyl-Hexyl 4.6 X 100 mm - N9308495Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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