Calibrachrom Lipsta XB-C18
Calibrachrom Lipsta XB-C18
- SKU
- NCC-101
- Phase
- XB-C18
- Pore size
- 120Å
- USP Class
- L1
- Separation Regime
- Reversed-Phase
- pH Range
- 2.0-8.0
- Surface area
- 320m2/g
- Carbon load
- 17 %
- Maximum pressure
- 40Mpa
- Endcapping
- Yes
- Temp Limits
- 60°C(pH≤6.5) and 40°C(pH>6.5)
- Particle Shape
- Spherical
Quantity
Calibrachrom Lipsta XB-C18
The Calibrachrom Lipsta XB-C18 chromatographic column is a fundamental component in chromatographic systems, widely used for industrial and laboratory analysis. Without a properly selected column, it is impossible to perform accurate research, determine composition, quantify substances, or verify purity.
Calibra Chrom for HPLC ensures high speed, accuracy, and reproducibility of results. They withstand high-pressure conditions and last for several years when maintained properly.
Calibrachrom Lipsta XB-C18 replaces
| Agilent ZORBAX Eclipse XDB-C18 |
| Agilent ZORBAX TYPE A Silica C18 |
| Agilent Pursuit XRs C18 |
| Agilent Pursuit XRs Ultra C18 |
| Agilent HC (2)/TC (2) HC-C18 (2) |
| Phenomenex Columbus C18 |
| Phenomenex Luna C18 |
| Phenomenex Luna Omega C18 |
| Phenomenex Prodigy ODS-2 |
| Sepax Sepax GP-C18 |
| Sepax Sepax Bio-C18-200 |
| Sepax Sepax Sapphire C18 |
| Supelco Discovery C18 |
| Supelco Discovery HS C18 |
| Thermo BETASIL C18 |
| Thermo Fluophase RP 100A perfluorohexyl |
| Thermo Hypersil GOLD C18 |
| Thermo Hypersil ODS (C18) |
| Thermo Hypersil ODS-2 (C18) |
| Thermo Acclaim 120 C18 |
| Thermo Acclaim AMG C18 |
| Thermo HyPURITY C18 |
| Thermo HyPURITY Aquastar |
| Thermo Syncronis C18 |
| Waters XBridge BEH 130-C18 (PST) |
| Waters XSelect HSS-C18 |
| Waters Symmetry C18 |
| Waters Sunfire C18 |
| Waters Spherisorb ODS2 fully end capped |
| Waters Delta-Pak C18 (100A) |
| Waters BioSuite C18 PA-A |
Compliance with Standards
To confirm compliance with strict quality requirements, Calibra Chrom columns underwent comprehensive testing.
The suitability of the chromatographic system was verified, and key validation parameters were assessed according to pharmacopoeial methods, including quality control of active pharmaceutical ingredients (APIs) and dosage forms (DFs).
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