Vitamin C Analysis Service

Vitamin C is highly unstable, leading to oxidation and nutrient loss in your products. Our advanced UHPLC-MS/MS and HPLC-based services accurately quantify AA, DHA, and derivatives, helping you achieve compliance and quality assurance without guesswork.

  • Optimize food and beverage shelf-life
  • Validate pharmaceutical formulations
  • Authenticate cosmetic actives
  • Support plant and biological research

Start your stability study today!

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What You Receive::

  • Raw & processed data files
  • Calibration curves & QC summary
  • Chromatograms & AA/DHA ratios
  • Customized interpretation report
  • What We Provide
  • Advantages
  • Technology Platform
  • Sample Requirement
  • Demo
  • FAQ

What is Vitamin C?

Vitamin C (ascorbic acid, AA) is a redox-active cofactor that stabilizes collagen cross-linking, maintains iron and copper in catalytically active states, and quenches reactive oxygen species in food, pharma, and biological matrices. Its intrinsic instability—rapid oxidation to dehydroascorbic acid (DHA) and further breakdown to diketogulonic acid—demands precise, time-sensitive quantification from sampling through reporting.

Why Quantify Vitamin C?—Decision-Critical Scenarios Our Clients Face

Your Business QuestionHow Accurate Vitamin C Analytics Unlock Better Decisions
Reformulating a beverage for extended shelf lifeTrack AA/DHA ratios to prove oxidative stability under accelerated storage tests.
Verifying label claims or regulatory complianceGenerate defensible certificates showing ±2 % accuracy across 1–1,000 µg mL⁻¹.
Profiling plant or microbial strains for metabolic engineeringMap intracellular Vitamin C flux together with redox-coupled metabolites.
Optimizing pharmaceutical dosage formsCharacterize ascorbyl derivatives (e.g., AAP, palmitate) to confirm pro-drug purity and conversion.

Creative Proteomics Vitamin C Analysis Solutions

Quantitative Analysis of AA & DHA

  • Sensitive detection of reduced and oxidized forms using UHPLC-MS or ECD-based HPLC
  • Ratio-based insights for oxidative stability and bioavailability studies

Degradation Pathway Mapping

  • Measurement of intermediate oxidation products like 2,3-diketogulonic acid
  • Ideal for stress-testing under thermal or oxidative conditions

Ester and Analog Quantification

Ascorbyl palmitate, phosphorylated derivatives, and isoascorbic acid quantified for formulation studies.

What We Measure—Comprehensive Vitamin C Panel

Analyte NameCAS NumberCategoryDetection Range (ng/mL)LOD (Limit of Detection)
Retinol68-26-8Preformed Vitamin C0.5 – 1,0000.1 ng/mL
Retinyl Palmitate79-81-2Retinyl Ester1 – 5,0000.5 ng/mL
Retinyl Acetate127-47-9Retinyl Ester1 – 5,0000.5 ng/mL
Retinaldehyde (Retinal)72-93-5Aldehyde Form1 – 2,0000.5 ng/mL
All-trans Retinoic Acid302-79-4Active Retinoid1 – 1,0000.2 ng/mL
13-cis Retinoic Acid4759-48-2Isomeric Retinoid1 – 1,0000.2 ng/mL
9-cis Retinoic Acid514-78-3Isomeric Retinoid1 – 1,0000.2 ng/mL
β-Carotene7235-40-7Provitamin A10 – 10,0001 ng/mL
α-Carotene7488-99-5Provitamin A10 – 10,0001 ng/mL
γ-Carotene7498-55-3Provitamin A Variant10 – 10,0001 ng/mL
Lycopene502-65-8Carotenoid10 – 10,0001 ng/mL
Cryptoxanthin472-70-8Provitamin A5 – 5,0001 ng/mL
Retinyl Propionate5808-35-7Retinyl Ester1 – 5,0000.5 ng/mL
Retinyl Stearate6106-24-7Retinyl Ester1 – 5,0000.5 ng/mL
11-cis Retinal17414-05-2Retinoid Intermediate1 – 1,0000.2 ng/mL

Distinct Advantages of Our Vitamin C Analysis Services

  • Sub-ppm Sensitivity: Limits of quantitation down to 10 ng mL⁻¹ for AA (signal-to-noise ≥ 10).
  • Linearity You Can Trust: r² ≥ 0.999 across three orders of magnitude, verified every 20 injections.
  • Repeatability that Cuts Re-runs: Intra-batch %RSD < 3 % (n = 6) for peak area and retention time.
  • True Recovery Verification: Spike-and-recovery of fortified blanks: 95 – 105 % for AA and DHA.
  • Minimal Matrix Interference: Isotope-dilution MS corrects ion suppression within ±5 %.

Workflow for Vitamin C Analysis Service

Step 1. Project Consultation & Method Selection

  • Define analytical objectives (quantification, derivative profiling, or stability study)
  • Recommend optimal method: UHPLC-MS/MS, HPLC-ECD, or combined platform

Step 2. Sample Receipt & Pre-Analysis Verification

  • Inspect sample integrity and verify storage conditions
  • Apply antioxidant stabilization protocols to minimize Vitamin C degradation

Step 3. Sample Preparation & Derivatization

  • Homogenization and extraction under cold, light-protected conditions
  • Optional derivatization for DHA stabilization using o-phenylenediamine (OPDA) or equivalent reagents

Step 4. Instrumental Analysis

  • Ultra-high performance liquid chromatography coupled with triple quadrupole MS or electrochemical detection
  • Multi-point calibration (r² ≥ 0.999) and isotope-labeled internal standards ensure accuracy

Step 5. Data Processing & Report Delivery

  • Quantitative results with AA/DHA ratio, degradation profile, and derivative levels
  • Comprehensive report includes chromatograms, calibration curves, and interpretation guidance

Our Vitamin C analysis workflow combines advanced sample stabilization, UHPLC-MS/MS detection, and rigorous QC protocols for reliable results.

Technology Platform for Vitamin C Analysis Service

Analytical MethodInstrument ModelKey ConditionsHighlight Features
UHPLC-MS/MS (Gold Standard) Thermo Fisher Vanquish + TSQ Altis Triple QuadrupoleC18 column (2.1 × 100 mm, 1.7 µm), 0.1% formic acid in water/methanol; ESI+; MRM modeUltra-sensitive quantification of AA and DHA; LOQ down to 10 ng/mL
UHPLC-HRMS (Structural Profiling) Thermo Scientific Vanquish + Q Exactive OrbitrapGradient separation; Full MS + PRMConfirms degradation products and derivative identity with accurate mass
HPLC-ECD (High Specificity) Antec DECADE Elite Electrochemical DetectorHILIC column; acetate bufferElectrochemical detection minimizes matrix interference; ideal for AA/DHA
HPLC-UV (Routine Analysis) Shimadzu LC-20A with SPD-20A UV DetectorC18 RP column; detection at 254 nmCost-effective solution for high-throughput QC testing
Ion Chromatography (Optional) Dionex ICS-5000+Ion-exchange column; citrate buffer; PDA detectionDirect analysis without derivatization; robust for high-salt matrices

Vitamin C Analytical Methods Performance Comparison

MethodInstrument ModelDetection Limit (LOQ)Linearity (r²)Repeatability (RSD%)
UHPLC-MS/MSThermo Vanquish + TSQ Altis0.01 µg/mL (10 ng/mL)≥ 0.999 across 0.01–1,000 µg/mL< 3%
UHPLC-HRMSVanquish + Q Exactive Orbitrap0.05 µg/mL≥ 0.999 across 0.05–1,000 µg/mL< 4%
HPLC-ECDAntec DECADE Elite0.02 µg/mL≥ 0.998 across 0.02–500 µg/mL< 3%
HPLC-UVShimadzu LC-20A0.10 µg/mL≥ 0.997 across 0.1–500 µg/mL< 5%
Ion Chromatography (PDA)Dionex ICS-5000+0.20 µg/mL≥ 0.996 across 0.2–500 µg/mL< 5%
Thermo Fisher Vanquish + TSQ Altis Triple Quadrupole

Thermo Fisher Vanquish + TSQ Altis Triple Quadrupole

Q Exactive™ UHMR Hybrid Quadrupole Orbitrap™ Mass Spectrometer

Q Exactive™ UHMR Hybrid Quadrupole Orbitrap™ Mass Spectrometer

Sample Requirements for Vitamin C Analysis Service

Sample TypeMinimum Amount RequiredRecommended Conditions
Fruit or Vegetable Tissue5 gFreeze immediately at −80 °C after homogenization; protect from light
Plant Leaves or Roots1–2 gStore in liquid nitrogen or at −80 °C; avoid repeated freeze-thaw
Food Products (Juices, Powders, Beverages)10 mL or 5 gStore at 4 °C for short term (<24h); −20 °C for longer storage
Pharmaceutical Formulations (Tablets, Capsules)5 units or 500 mgProtect from moisture; store at room temperature in light-proof container
Biological Fluids (Plasma, Serum)200 µLStabilize with antioxidant (e.g., metaphosphoric acid) immediately upon collection
Fermentation Broth / Cell Culture Media2 mLCollect under cold conditions; freeze at −80 °C
Cosmetic Products (Creams, Lotions)3 gSeal tightly; avoid exposure to light and heat

Tip: Always use amber vials or wrap samples in aluminum foil to prevent oxidation during shipping.

Demo Results

Chromatogram with two peaks for AA and DHA, retention times ~2.8 and ~4.5 min.

Figure 1. Representative chromatogram showing clear separation of ascorbic acid (AA) and dehydroascorbic acid (DHA).

Calibration curves of AA and DHA with peak area vs concentration, r² ≥ 0.999.

Figure 2. Calibration curves for ascorbic acid (AA) and dehydroascorbic acid (DHA) showing excellent linearity (r² ≥ 0.999) across 0.01–1000 µg/mL.

QC table showing AA and DHA recovery (95–102%) and precision (RSD < 3%).

Figure 3. Quality control results for AA and DHA with recovery between 95–102% and RSD < 3%, confirming high accuracy and reproducibility.

Bar chart of AA and DHA concentrations in orange juice, vitamin drink, tablet, and leaf.

Figure 4. Vitamin C content in different samples (orange juice, vitamin drink, tablet, and leaf) showing AA as major component and DHA as minor fraction.

FAQ of Vitamin C Analysis Service

Can you analyze both reduced and oxidized forms of Vitamin C in one run?

Yes. Our UHPLC-MS/MS and UHPLC-ECD methods allow simultaneous detection of ascorbic acid (AA) and dehydroascorbic acid (DHA) in a single injection, preserving redox balance information.

How do you prevent Vitamin C degradation during sample handling?

We recommend using stabilizers such as metaphosphoric acid and maintaining samples at low temperatures. Our technical team provides detailed stabilization protocols and pre-treated collection vials upon request.

Do you provide profiling for Vitamin C derivatives and esters?

Yes. In addition to AA and DHA, we can quantify derivatives such as ascorbyl palmitate, ascorbyl phosphate, and isoascorbic acid. Customized panels are available for nutraceutical, food, and pharmaceutical studies.

Can you perform stability or stress testing for Vitamin C-containing products?

Yes. We design oxidative and thermal stress testing protocols to evaluate Vitamin C degradation kinetics and provide data that support shelf-life predictions.

How do you ensure analytical accuracy and reproducibility?

We apply isotopically labeled internal standards, multi-point calibration (r² ≥ 0.999), and include spike-recovery and QC checks in every batch to guarantee reliable results.

Can you integrate Vitamin C analysis into multi-nutrient or metabolomics studies?

Absolutely. Vitamin C quantification can be combined with other micronutrient, antioxidant, or metabolite profiling services, giving a comprehensive view of redox metabolism.

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Publications

Here are some of the metabolomics-related papers published by our clients:

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Metabolomics Sample Submission Guidelines

Download our Metabolomics Sample Preparation Guide for essential instructions on proper sample collection, storage, and transport for optimal experimental results. The guide covers various sample types, including tissues, serum, urine, and cells, along with quantity requirements for untargeted and targeted metabolomics.

Metabolomics Sample Submission Guidelines
* For Research Use Only. Not for use in diagnostic procedures.
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