GC/MS Residual Solvent Analyzers
Agilent's flexible, pre-configured and factory-tested Residual Solvent Analyzers provide quick start-up for accurate and reproducible analysis of Class 1 and Class 2A/B solvent content in pharmaceutical products.
GC/MS Residual Solvent Analyzers
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Had to get support external to Agilent.
Hydrocarbon analysis
Currently switching from the He to Hz carrier. Aduire from Agilent only partially helpful around this switch. The switch is going well but MS was highly variable. Tech support external to Agilent has traced the problem to a MS that is not compatible with Hz and carrier flow that is too high for turbo. Would have liked to get this information from Agilent sooner.
Review Date: 12 Mar 2020 | Agilent Technologies
Regulatory bodies such as ICH, USP, and EP define limits for residual volatile organic chemicals in pharmaceutical formulations. To meet these guidelines, producers must monitor solvent levels in finished products, active ingredients and additives. Agilent's flexible, pre-configured and factory-tested Residual Solvent Analyzers provide quick start-up for accurate and reproducible analysis of Class 1 and Class 2A/B solvent content in pharmaceutical products.
With an inert sample path and excellent thermal zone stability, the Agilent 7697A Headspace Sampler automates sample handling to provide unsurpassed accuracy and repeatability combined with analytical precision that exceeds USP method requirements. Choose from the 7890-based GC/FID or GC/FID/MS system configurations designed to meet your specific monitoring requirements.
Features:
- Configured to meet the requirements for USP <467> including column, consumables, calibration/checkout samples, and analytical method facilitates adaptation to your laboratory's SOPs.
- GC/MS/FID analysis provides identification and confirmation of organic contaminants in pharmaceutical active ingredients, formulations and additives.
- Headspace thermal zone stability of ±0.1 °C, inert flow path, and use of patented Capillary Flow Technology (CFT) provides ≤3% for USP Class 1A and Class 2A/B solvents.
- Pre-configured per industry standards and chemically tested ensuring optimal analysis of Class 1 and Class 2A/B Solvents in pharmaceutical products.
- Includes CD-ROM with optimized acquisition method for Residual Solvent Analysis and quick start guide for faster method validation.
- On-site installation and check out of the Analyzer performance by a factory certified technician confirms that your instrument and application meet Agilent’s analytical performance criteria.
