Educational

HPLC vs. GC-MS: Understanding Purity Verification Methods

HPLC vs. GC-MS: Understanding Purity Verification Methods

How analytical chemistry ensures the ≥98% purity standard of ELITE CHEMS research compounds.

Scientific review by DR. James, Analytical Chemistry Director

When you receive a Certificate of Analysis (CoA) with your order, it represents hours of advanced instrumentation work. Here's how we validate purity.

HPLC: The Gold Standard

▲ How It Works

High-Performance Liquid Chromatography separates compounds using:

  • Polarity gradients in mobile phase
  • C18 reverse-phase columns
  • UV-VIS detection (190-400nm)

◉ Our Protocol

All batch-tested products undergo:

  • Triplicate injections
  • USP-grade reference standards
  • 0.5% RSD threshold

GC-MS: Volatile Compound Analysis

When We Use GC-MS

For low-molecular-weight compounds like:

  • Cathinones (MW < 250)
  • Piperazines
  • Volatile novel analogs

Detection limits: 0.1% impurity threshold with EI ionization

Side-by-Side Comparison

Parameter HPLC-UV GC-MS
Ideal for Peptides, polar compounds Volatile small molecules
Detection Limit 0.5% impurities 0.1% impurities
Sample Prep Dissolution in mobile phase Derivatization often needed

Request Your CoA

Every ELITE CHEMS product includes batch-specific purity data. Contact us for full analytical reports.

VIEW CERTIFIED PRODUCTS

Why This Matters for Your Research

▼ Reproducible Results

Our HPLC-tested peptides eliminate batch variability

▼ Impurity Profiling

GC-MS identifies synthesis byproducts in synthetic cannabinoids

Technical Deep Dive

Our lab uses these instrument configurations:

HPLC Specifications

  • System: Agilent 1260 Infinity II
  • Column: Zorbax Eclipse Plus C18 (4.6×150mm, 3.5µm)
  • Method: 10-90% ACN in H2O (0.1% TFA) over 20min

For researchers requiring analytical documentation, we provide:

  1. Raw chromatograms upon request
  2. Method validation reports for bulk orders

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