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CoMetro CP-LDI Parallel Dual-Head Precision Constant-Flow HPLC Pump

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Brand CoMetro
Origin Imported
Manufacturer Type Authorized Distributor
Model CP-LDI Dual-Head
Flow Rate 0.001–12 mL/min (configurable up to 200 mL/min)
Maximum Pressure 6000 psi
Accuracy ±1%
Precision ≤0.1% RSD
Pump Head Configuration Parallel Dual-Head
Pressure Units psi / MPa / bar
Control Modes Front-panel keypad, RS-232/USB PC interface, analog input (0–5 V or 4–20 mA)
Compressibility Compensation Adjustable
Auto-Purge & Self-Cleaning Mode Supported for salt-containing mobile phases

Overview

The CoMetro CP-LDI Parallel Dual-Head Precision Constant-Flow HPLC Pump is an engineered solution for high-pressure liquid delivery in analytical, semi-preparative, and preparative chromatography systems. Designed around a dual-piston, parallel-driven architecture, it delivers stable, pulse-free solvent flow under sustained high backpressure—up to 6000 psi (414 bar)—making it suitable for applications involving sub-2-µm particle columns, UHPLC-compatible media, and viscous mobile phases. Its core operational principle relies on synchronized stepper motor actuation of two independently sealed pump heads, with real-time pressure feedback from integrated piezoresistive transducers enabling dynamic compressibility compensation. This closed-loop hydraulic control architecture ensures consistent volumetric displacement across varying solvent compressibility and system impedance—critical for gradient reproducibility and retention time stability in regulated environments.

Key Features

  • Parallel dual-head design eliminates pulsation and enhances flow continuity without requiring active dampening hardware
  • Adjustable compressibility compensation algorithm mitigates solvent-dependent volume loss, improving accuracy across acetonitrile/water, methanol/water, and buffer-based gradients
  • Front-panel keypad with high-brightness LED display enables local operation with real-time monitoring of flow rate (0.001–12 mL/min, expandable to 200 mL/min via optional configuration), pressure (psi/MPa/bar), and system status
  • Multiple control interfaces: standalone keypad, RS-232/USB-connected PC software, and analog voltage/current inputs for integration into legacy or custom-built chromatographic platforms
  • Programmable pressure limits (low/high) with automatic shutdown and alarm logging compliant with ICH Q2(R2) instrument qualification requirements
  • Auto-purge and self-cleaning cycle specifically optimized for phosphate- and acetate-buffered mobile phases—reducing crystallization risk on plunger seals and extending service intervals
  • Modular scalability: systems may be expanded to support 2-, 3-, or 4-pump configurations for quaternary or ternary gradient formation, satisfying USP and ASTM D7977 method flexibility criteria

Sample Compatibility & Compliance

The CP-LDI is compatible with common HPLC solvents including water, acetonitrile, methanol, isopropanol, THF, and dilute aqueous buffers (pH 2–9). Its wetted parts—stainless steel 316L pump heads, sapphire-ruby check valves, and PEEK/PTFE fluidic pathways—are chemically resistant to aggressive mobile phases used in peptide purification, natural product isolation, and pharmaceutical impurity profiling. The pump meets mechanical safety standards per IEC 61010-1 and supports GLP/GMP workflows through audit-trail-enabled software (optional CoMetro ChromoControl Suite), which records all parameter changes, error events, and maintenance logs with user authentication and timestamping—fully aligned with FDA 21 CFR Part 11 data integrity requirements.

Software & Data Management

The optional ChromoControl Suite provides full remote configuration, method storage, and real-time telemetry visualization. It supports method transfer between instruments, automated calibration report generation (per ISO/IEC 17025), and export of CSV-formatted pressure/flow logs for statistical process control (SPC) analysis. All parameter modifications are logged with operator ID, timestamp, and pre-/post-change values. Firmware updates are delivered via signed binary packages to ensure traceability and prevent unauthorized modification—essential for laboratories undergoing regulatory inspection by EMA, PMDA, or ANVISA.

Applications

  • Isocratic and multi-step gradient elution in QC release testing of APIs and excipients (per USP , EP 2.2.46)
  • Semi-preparative purification of monoclonal antibodies and ADC intermediates using wide-bore columns (10–30 mm ID)
  • Method development for chiral separations requiring precise flow ramping and low-pressure dwell volume
  • Integration into automated fraction collection systems for natural product dereplication
  • Use as auxiliary pump in LC-MS systems for post-column derivatization or sheath liquid delivery
  • Support for accelerated solvent extraction (ASE) and supercritical fluid chromatography (SFC) auxiliary fluid delivery where constant flow at moderate pressure is required

FAQ

What is the minimum programmable flow rate, and how is low-flow stability achieved?
The CP-LDI achieves 0.001 mL/min resolution via microstepping motor control and adaptive dwell-volume compensation; flow stability at this range is maintained by real-time pressure feedback and dynamic piston position correction.
Can the pump operate continuously at 6000 psi without performance degradation?
Yes—the dual-head architecture distributes mechanical load, and thermal management includes passive heat-sink design and duty-cycle monitoring to prevent seal overheating during extended high-pressure operation.
Is the system compatible with third-party chromatography data systems (CDS)?
It supports standard ASCII command protocols over RS-232/USB and offers optional OPC UA server integration for seamless connection to Waters Empower, Thermo Chromeleon, or Agilent OpenLab CDS.
How does the self-cleaning function protect against buffer precipitation?
The protocol sequentially flushes pump heads with high-purity water followed by organic solvent at elevated flow rates, then applies reverse-direction priming pulses to evacuate residual crystals from check valve seats.
What documentation is provided for IQ/OQ/PQ validation?
CoMetro supplies a complete validation package including URS template, FAT/SAT reports, calibration certificates traceable to NIST standards, and a PQ protocol with acceptance criteria aligned with ASTM E2656 and ISO 9001 clause 7.6.

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