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Agilent 7696A Sample Preparation Workstation

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Brand Agilent Technologies
Origin Shanghai, China
Manufacturer Type Original Equipment Manufacturer (OEM)
Regional Classification Domestic (China-manufactured)
Model 7696A
Pricing Upon Request
Instrument Type Gas Chromatography (GC) Autosampler-Integrated Offline Sample Preparation System

Overview

The Agilent 7696A Sample Preparation Workstation is an offline, benchtop automation platform engineered for reproducible, method-driven sample preparation prior to gas chromatography (GC) analysis. Unlike integrated autosamplers that inject directly into the GC inlet, the 7696A operates independently—performing critical preparatory steps including precise liquid dispensing, serial dilution, internal standard addition, reconstitution, small-volume liquid–liquid extraction (LLE), and controlled derivatization reactions. Its design follows the principle of “pre-analytical automation”: by decoupling sample conditioning from instrument runtime, laboratories achieve higher GC instrument utilization, reduced manual intervention, and improved inter-operator consistency. The system employs positive-displacement liquid handling technology with calibrated syringe-based pipetting modules, ensuring volumetric accuracy across a wide dynamic range (typically 1–1000 µL) and high repeatability (CV < 1.5% at ≥10 µL). It is not a GC injector per se but a dedicated pre-injection workflow engine compliant with GLP/GMP-aligned laboratory practices.

Key Features

  • Modular liquid handling tower with dual independent syringe pumps for simultaneous or sequential aspiration/dispense operations
  • Integrated heating block (ambient to 100 °C) supporting temperature-controlled derivatization, hydrolysis, or solvent evaporation steps
  • Programmable vortex mixer with adjustable speed (300–2500 rpm) and timed activation for homogeneous sample reconstitution
  • Barcode reader compatibility for full sample traceability—each vial scanned upon loading triggers automatic method assignment and audit trail generation
  • Easy SamplePrep software with drag-and-drop workflow builder, real-time status monitoring, and electronic logbook compliant with FDA 21 CFR Part 11 requirements (user authentication, electronic signatures, audit trail export)
  • Compact footprint (W × D × H: 60 × 65 × 55 cm) designed for ventilation hood installation—fully enclosed reagent handling minimizes operator exposure to volatile organics and hazardous derivatizing agents

Sample Compatibility & Compliance

The 7696A accommodates up to 150 × 2 mL screw-thread vials in standardized racks, compatible with common GC/LC autosampler trays (e.g., Agilent 7693/7697 series). It supports aqueous, organic, and mixed-phase matrices—including biological fluids (plasma, urine), environmental extracts (soil leachates, wastewater), and food homogenates. All fluidic pathways are chemically resistant to acetonitrile, methanol, chloroform, and acidic/basic reagents. The workstation meets IEC 61000-6-3 (EMC) and IEC 61010-1 (safety) standards. Its software architecture supports ALCOA+ data integrity principles and is validated for use in regulated environments governed by ISO/IEC 17025, USP , and ASTM D7097 (for environmental GC analysis workflows).

Software & Data Management

Easy SamplePrep provides a graphical workflow editor where users define step-by-step protocols using modular icons: “Dispense”, “Heat”, “Vortex”, “Wait”, “Barcode Scan”, and “Transfer”. Each step includes parameter fields for volume, temperature, duration, and mixing intensity. Protocols are version-controlled and digitally signed. Raw execution logs—including timestamps, syringe positions, actual dispensed volumes (from encoder feedback), and error codes—are stored in encrypted SQLite databases. Audit trails are exportable as PDF or CSV and include operator ID, method revision, and system event history. Optional integration with Agilent OpenLab CDS enables direct protocol push and post-run metadata synchronization.

Applications

  • Residue analysis in agrochemical testing (e.g., EPA Method 525.3 for pesticides in drinking water)
  • Pharmaceutical impurity profiling requiring derivatization (e.g., aldehyde/ketone analysis via PFBHA derivatization prior to GC-ECD)
  • Environmental monitoring of semi-volatile organic compounds (SVOCs) per EPA Method 8270D
  • Clinical toxicology workflows involving internal standard normalization and enzymatic hydrolysis of glucuronide-conjugated drugs
  • Food safety labs performing fatty acid methyl ester (FAME) analysis via BF₃-catalyzed transesterification

FAQ

Is the 7696A compatible with non-Agilent GC systems?
Yes—the workstation outputs prepared samples in standard 2 mL vials; these can be loaded manually or via third-party autosamplers supporting ANSI/SBS rack formats.
Does it support solid-phase extraction (SPE) cartridge processing?
No—SPE requires vacuum or positive-pressure manifolds; the 7696A is optimized for liquid-phase manipulations only (dilution, LLE, derivatization, reconstitution).
Can methods be exported between instruments?
Yes—protocols are saved as .xml files and are portable across all 7696A units running the same Easy SamplePrep firmware version.
What maintenance is required for long-term precision?
Monthly calibration verification using gravimetric checks and quarterly syringe seal replacement—documented in the built-in preventive maintenance scheduler.
Is remote monitoring supported?
Yes—via secure HTTPS interface; administrators can view real-time run status, receive email alerts on completion or fault, and access archived logs through role-based web portal.

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