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Millipore MilliQ Advantage Ultra Pure Water System

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Brand Millipore
Origin France
Model MilliQ Advantage
Production Rate Up to 2 L/min
Resistivity 18.2 MΩ·cm @ 25 °C
TOC ≤5 ppb
Particles (>0.22 µm) <1 particle/mL
Bacteria <1 CFU/mL
Endotoxins <0.001 EU/mL (with BioPak)
RNases <0.01 ng/mL (with BioPak)
DNases <4 pg/mL (with BioPak)
Terminal Filtration Options MilliPak (0.22 µm), BioPak (ultrafiltration), EDS Pak, VOC-Pak
Compliance ASTM D1125-95 (1999), USP <1231>, EP 2.2.44, ISO 3696 Grade 1, CAP/NCCL I-grade water specifications

Overview

The Millipore MilliQ Advantage Ultra Pure Water System is a modular, high-performance laboratory water purification platform engineered for precision-critical applications in analytical chemistry, life sciences, and regulatory-compliant research environments. Designed to operate with pre-treated feed water—such as reverse osmosis (RO), distillation, deionization, or Elix-generated purified water—the system integrates multi-stage purification technologies including dual-wavelength UV oxidation (185/254 nm), electrodeionization (EDI), and selective terminal filtration to consistently deliver Type I ultrapure water meeting stringent international standards. Its core architecture employs a closed-loop recirculation loop with continuous monitoring, minimizing stagnation and ensuring microbiological stability. The system’s measurement foundation rests on real-time, temperature-compensated resistivity detection (electrode constant <0.1 cm⁻¹, compliant with ASTM D1125-95 (1999)) and online total organic carbon (TOC) analysis (1–999 ppb range), enabling trace-level organic and ionic contaminant control essential for HPLC, LC-MS, ICP-MS, and molecular biology workflows.

Key Features

  • Modular terminal purification: Selectable cartridges—including MilliPak Express (0.22 µm hydrophilic PVDF membrane), BioPak (10 kDa ultrafiltration for endotoxin/RNase/DNase removal), EDS Pak (endocrine disruptor study support), and VOC-Pak (volatile organic compound elimination)—allow application-specific water quality tailoring.
  • Intelligent POD (Point-of-Delivery) interface: Wall-mountable, 360° rotatable, height-adjustable dispensing arm with integrated color touchscreen displaying real-time resistivity, TOC, temperature, flow rate, and cartridge lifetime status—enabling full operational awareness without accessing the main unit.
  • Dual-parameter continuous monitoring: Patented online TOC analyzer coupled with high-accuracy, temperature-compensated conductivity sensor (±0.1 °C resolution) ensures metrological traceability and compliance with USP , EP 2.2.44, and ISO 3696 Grade 1 requirements.
  • Automated system management: Embedded firmware supports scheduled maintenance alerts, usage logging, user role assignment (administrator vs. operator), and password-protected parameter locking—facilitating GLP/GMP-aligned operation and audit readiness.
  • Four programmable flow rates (including up to 2 L/min maximum), quantitative dispensing mode, and low-footprint design optimize workflow integration across benchtop, hood, and centralized lab configurations.

Sample Compatibility & Compliance

The MilliQ Advantage delivers water suitable for the most demanding analytical and biological applications. With MilliPak terminal filtration, output meets specifications for HPLC mobile phase preparation, LC-MS solvent compatibility, MALDI-TOF matrix dissolution, ion chromatography (IC), inductively coupled plasma (ICP) spectroscopy, and atomic absorption (AA) analysis. When configured with BioPak, the system produces water equivalent to DEPC-treated water—validated for PCR, qRT-PCR, cell culture media preparation, transfection, and stem cell work. All configurations comply with ASTM D1125-95 (1999) for conductivity measurement accuracy, USP for pharmaceutical water quality, and ISO 3696:2017 Grade 1 specifications. The system supports 21 CFR Part 11–ready data integrity when connected to compatible LIMS or enterprise software via optional Ethernet or RS232 interfaces.

Software & Data Management

The embedded operating system provides comprehensive data governance capabilities: automatic timestamped event logging (cartridge changes, alarms, maintenance cycles), user-access audit trails, and exportable CSV reports for quality documentation. Optional connectivity modules enable remote system status monitoring, predictive cartridge replacement scheduling, and integration into centralized laboratory informatics platforms. All stored parameters—including resistivity drift trends, TOC excursions, and flow history—are retained with tamper-evident timestamps, supporting FDA-regulated environments requiring ALCOA+ (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available) data principles.

Applications

  • High-sensitivity analytical instrumentation: HPLC, UHPLC, LC-MS/MS, GC-MS, ICP-OES, ICP-MS, AAS, IC.
  • Molecular biology: DNA/RNA extraction, cloning, sequencing library prep, CRISPR editing, primary cell culture, organoid maintenance.
  • Pharmaceutical R&D and QC: Buffer preparation for biologics formulation, reference standard dilution, dissolution testing, extractables/leachables studies.
  • Environmental and toxicology research: Endocrine disruptor screening (EDS), PFAS analysis, low-level contaminant quantification requiring VOC-free matrices.
  • Clinical diagnostics: CAP-accredited clinical chemistry assays, NGS-based pathogen detection, companion diagnostic reagent preparation.

FAQ

What feed water quality is required for optimal MilliQ Advantage performance?
The system requires pretreated water with resistivity ≥0.05 MΩ·cm (≥20 µS/cm conductivity) and silica <500 µg/L—typically supplied by RO, distillation, or Elix systems. Inadequate feed quality accelerates consumable wear and compromises final water purity.
Can the MilliQ Advantage be validated per IQ/OQ/PQ protocols?
Yes. Full validation documentation packages—including test protocols, acceptance criteria, and blank templates aligned with ISO/IEC 17025 and GAMP5—are available upon request. The system’s built-in calibration logs and alarm history support formal qualification.
Is TOC monitoring mandatory, or can it be disabled?
TOC monitoring is integral to the system’s real-time water quality assurance architecture and cannot be disabled; however, its calibration and verification procedures are fully documented and compliant with ASTM D5542 and USP .
How often must terminal filters be replaced?
Replacement intervals depend on usage volume and feed water quality: MilliPak cartridges are rated for up to 1,000 L; BioPak for 500 L; EDS Pak and VOC-Pak for 300 L. The POD display provides real-time cartridge saturation indicators and automated replacement reminders.
Does the system support networked user authentication?
Yes. Role-based access control (administrator/operator) with password protection is standard. Optional LDAP or Active Directory integration is supported via the Ethernet communication module for enterprise-wide identity management.

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