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Canadian Independent Laboratory

Independent Peptide Testing & Analytical Services

Reliable analytical testing, purity verification, and professional laboratory reporting. Trusted results for researchers, manufacturers, and biotech companies across Canada and beyond.

HPLC
Purity Analysis
MS
Identity Confirmation
COA
Certified Reports
HPLC Purity Analysis
High-performance liquid chromatography
Active
Mass Spectrometry
Molecular identity verification
Active
FTIR Spectroscopy
Functional group identification
Active
Gly Ala Lys Pro —NH— —CO— —NH— H₂N— —COOH Peptide Chain · Structural Analysis
HPLC Purity Analysis ≥ 98.5%
Mass Spectrometry ID Confirmed
Moisture Content (KF) 4.2% w/w
COA Issued with Every Test ✓ Included
Independent Testing
No conflicts of interest — unbiased results you can trust
Fast Turnaround
Efficient processing without compromising accuracy
Professional Reporting
Clear, comprehensive analytical documentation
Confidential Service
Strict sample handling with full data privacy
HPLC-UV MASS-SPEC C · O · A PASS NORTHERN PEPTIDE LABS · ANALYTICAL LABORATORY
100%
Independent & Unbiased
🍁 Based in Canada
About Northern Peptide Labs

Precision You Can Rely On

Northern Peptide Labs is an independent Canadian analytical laboratory providing rigorous quality verification, purity testing, and compound identification services for peptides, research chemicals, and biotechnology products.

Our mission is to deliver accurate, transparent, and timely analytical results — giving researchers, manufacturers, and biotech companies the reliable data they need to make informed decisions with confidence.

Fully independent — results driven solely by science, not commercial interests
Modern analytical equipment including HPLC, MS, and FTIR systems
Comprehensive Certificates of Analysis issued for every sample
Strict confidentiality protocols — your data stays private
Analytical Services

Comprehensive Testing Solutions

Industry-standard analytical methods to verify the purity, identity, and quality of your compounds.

Why Choose Us

The Standard for Independent Peptide Testing

When accuracy matters, researchers and manufacturers choose Northern Peptide Labs for our commitment to analytical rigour, transparency, and impartial reporting.

Independent Laboratory

No affiliations with manufacturers or suppliers

Modern Equipment

State-of-the-art analytical instrumentation

Fast Turnaround

Results delivered efficiently without compromise

Confidential Handling

Strict privacy protocols for every sample

Detailed Reports

Comprehensive, clearly formatted documentation

Reliable & Accurate

Validated methods with rigorous quality control

1
Submit Your Request
Fill out our quote form specifying your compound and required tests
2
Send Your Sample
Ship your sample to our facility using our secure submission guidelines
3
Laboratory Analysis
Our scientists run the appropriate analytical tests on your sample
4
Receive Your Results
A professional COA and full test report is delivered securely
Get Started

Request a Laboratory Quote

Tell us about your compound and testing needs. We'll respond with a detailed quote and sample submission instructions within one business day.

No obligation quote within 24 hours
Competitive pricing for all analytical services
Confidential — your information is never shared
Available for Canadian and international clients

Contact Our Laboratory

🔒 All information is kept strictly confidential

Quote Request Sent!

Thank you. Our team will review your request and respond within one business day.

Analytical Service

HPLC Analysis

High-Performance Liquid Chromatography — the industry standard for peptide purity determination and quantitative compound analysis.

What is HPLC?

High-Performance Liquid Chromatography (HPLC) is a powerful analytical technique used to separate, identify, and quantify individual components within a mixture. It is the most widely used method in the pharmaceutical, biotechnology, and research industries for determining the purity of peptides and research compounds.

In HPLC analysis, a liquid sample is dissolved in a solvent and pushed under high pressure through a column packed with stationary phase material. Different molecules interact with the stationary phase to varying degrees, causing them to travel through the column at different rates and emerge separately — a process called chromatographic separation.

How Does HPLC Work?

The sample is injected into the system and carried by a mobile phase (solvent) through a stationary phase (the column). As compounds pass through, a UV detector records when each component exits, generating a chromatogram — a graph of peaks representing each separated compound. The area of each peak is directly proportional to the amount of that compound present in the sample.

  • Sample is dissolved and injected into the HPLC system
  • High-pressure pump drives the mobile phase through the column
  • Compounds separate based on their affinity for the stationary phase
  • UV detector records each compound as it elutes from the column
  • Data is processed to calculate purity percentages for each peak

What Does the Result Tell You?

The HPLC chromatogram shows the purity of your compound as a percentage. For example, a result of 98.5% purity means that 98.5% of the detected material corresponds to your target compound, with the remaining 1.5% consisting of impurities, degradation products, or related compounds. This information is essential for verifying product quality and ensuring accurate dosing in research applications.

Why Is HPLC the Industry Standard?

HPLC is trusted across industries because it delivers precise, reproducible, and quantitative results. Unlike visual or qualitative assessments, HPLC provides an objective numerical purity value backed by physical separation of compounds.

  • Detects impurities at very low concentrations
  • Provides a quantitative purity percentage — not just a pass/fail
  • Widely accepted by regulatory agencies and research institutions
  • Reproducible and validated methodology
  • Applicable to a broad range of peptides and research compounds

At Northern Peptide Labs, our HPLC analysis is performed using reverse-phase methodology — the standard approach for peptide purity testing — and all results are reported in a professional Certificate of Analysis.

Analytical Service

Mass Spectrometry

Definitive molecular identity confirmation using precise mass-to-charge ratio analysis — verifying exactly what your compound is.

What is Mass Spectrometry?

Mass Spectrometry (MS) is an analytical technique that measures the mass of molecules with extraordinary precision. By determining the exact molecular weight of a compound, MS provides definitive identity confirmation — telling you not just how pure a sample is, but confirming that the compound itself is what it is claimed to be.

For peptide analysis, MS is an essential tool because peptides can have similar physical properties yet completely different structures. A purity test alone cannot confirm identity — only mass spectrometry can verify that the correct amino acid sequence and molecular structure are present.

How Does Mass Spectrometry Work?

In mass spectrometry, the sample is first ionized — molecules are given an electrical charge. These ions are then accelerated through a mass analyzer, which separates them according to their mass-to-charge ratio (m/z). A detector records the signal at each mass value, producing a mass spectrum — a plot showing which masses are present and in what abundance.

  • Sample is dissolved and introduced into the MS system
  • Ionization converts neutral molecules into charged ions (commonly via ESI for peptides)
  • Ions are separated in the mass analyzer based on their m/z ratio
  • The detector records each ion, generating a mass spectrum
  • The observed mass is compared to the theoretical molecular weight of the compound

How Is Identity Confirmed?

Each compound has a unique theoretical molecular weight calculated from its molecular formula. When the mass spectrum shows a major peak at or very close to this expected mass, the identity of the compound is confirmed. For peptides, additional fragmentation patterns (MS/MS) can further verify the amino acid sequence, providing an even higher level of structural certainty.

Why Is MS Often Combined with HPLC?

HPLC and Mass Spectrometry are highly complementary techniques. HPLC tells you how pure a compound is (percentage-wise), while MS tells you what the compound actually is. Together, they provide a complete analytical picture — purity and identity — which is why HPLC-MS is the most comprehensive and trusted approach for peptide characterization.

  • HPLC provides quantitative purity data; MS provides identity confirmation
  • Neither technique alone is fully sufficient for complete characterization
  • Together they satisfy the highest analytical standards
  • The HPLC-MS combination is specified by most regulatory frameworks
  • Provides the strongest possible documentation for a Certificate of Analysis

Northern Peptide Labs offers standalone MS testing as well as combined HPLC + MS packages, ensuring your samples are characterized with the most thorough analytical approach available.

Analytical Service

FTIR Analysis

Fourier-Transform Infrared Spectroscopy for functional group identification, material characterization, and excipient verification.

What is FTIR?

Fourier-Transform Infrared Spectroscopy (FTIR) is a non-destructive analytical technique that identifies chemical compounds by measuring how they absorb infrared (IR) light. Every functional group — the chemical building blocks of molecules — absorbs IR radiation at specific, characteristic wavelengths, creating a unique spectral "fingerprint" for each material.

FTIR is widely used in pharmaceutical and materials science applications to identify compounds, verify excipients, detect contaminants, and confirm the structural integrity of a substance.

How Does Infrared Spectroscopy Work?

In FTIR analysis, infrared light is passed through or reflected off the sample. The instrument measures which wavelengths of IR light are absorbed by the sample and which are transmitted. This absorption pattern is converted mathematically (via a Fourier Transform) into an infrared spectrum — a graph showing characteristic absorption peaks.

  • Infrared light passes through or reflects off the sample
  • Chemical bonds absorb IR energy at their characteristic frequencies
  • The detector measures transmitted or reflected light intensity
  • A Fourier Transform converts raw data into a readable spectrum
  • The spectrum is compared to reference libraries for identification

What Data Can You Obtain from FTIR?

FTIR provides qualitative and semi-quantitative information about the chemical composition of a sample. Key data includes identification of functional groups (amide bonds, hydroxyl groups, carbonyl groups, etc.), confirmation of material class, and detection of contaminants or adulterants.

  • Identification of major functional groups present in the compound
  • Detection of unexpected or foreign chemical entities
  • Confirmation of excipients (e.g., acetic acid salt forms in peptides)
  • Comparison to reference spectra for identity screening
  • Verification of material class and general structural features

Advantages & Limitations

FTIR is fast, non-destructive, and requires minimal sample preparation, making it ideal for routine material screening and excipient verification. However, it is primarily a qualitative tool — it identifies what is present but does not readily quantify purity percentages as HPLC does. For complex mixtures or low-level impurity detection, HPLC or MS are more appropriate. FTIR is most valuable as a complementary technique or as a standalone screening method for solid materials and excipient confirmation.

For Which Materials Is FTIR Applied?

FTIR is applicable to virtually any solid, liquid, or gas-phase material, making it one of the most versatile analytical techniques available. Common applications in our laboratory include:

  • Lyophilized (freeze-dried) peptide powders
  • Excipient and salt form verification (e.g., acetate vs. trifluoroacetate)
  • Raw materials and starting material characterization
  • Polymer and excipient identification
  • Contaminant and adulterant screening
Analytical Service

Moisture Content Testing

Precise water content determination using Karl Fischer titration — essential for product stability and accurate potency assessment.

What is Moisture Content Analysis?

Moisture content testing measures the amount of water present within a compound sample, expressed as a weight percentage. Water is a natural component of many lyophilized peptides and research compounds, and its level directly impacts product stability, accurate weight-based dosing, and long-term storage performance.

At Northern Peptide Labs, we use Karl Fischer (KF) titration — the gold standard method for water content determination — which provides specific and highly precise results for moisture in the range of 0.01% and above.

Why Does Moisture Content Matter?

Many researchers and manufacturers underestimate the importance of moisture content in peptide products. Lyophilized peptides commonly contain between 1–10% water by weight, and this water content is not always accounted for when calculating dosing. Understanding moisture content is critical for several reasons:

  • Accurate potency calculation — water content reduces the actual active compound percentage
  • Product stability — excessive moisture accelerates chemical degradation and aggregation
  • Shelf-life assessment — moisture is a primary driver of peptide decomposition over time
  • Storage condition validation — confirms whether drying or lyophilization was effective
  • Regulatory compliance — moisture limits are specified for many pharmaceutical compounds

Karl Fischer Titration — The Gold Standard

Karl Fischer titration is a highly specific electrochemical method that reacts exclusively with water molecules, making it far more accurate than gravimetric (loss-on-drying) approaches. It detects only water — not other volatile components — and delivers precise results even at low moisture levels. This method is specified by major pharmacopoeias (USP, BP, EP) as the reference procedure for water content determination.

How Does It Affect Product Stability?

Water is a key driver of chemical reactions that degrade peptides and research compounds over time. Even small amounts of excess moisture can catalyze oxidation, hydrolysis, and racemization — reactions that break down active compounds and reduce product potency. Maintaining moisture below critical thresholds is therefore essential for achieving the expected shelf-life of a product.

  • High moisture promotes peptide bond hydrolysis and sequence degradation
  • Water facilitates oxidation of methionine, tryptophan, and cysteine residues
  • Moisture accelerates microbial growth risk in non-sterile compounds
  • Proper moisture data supports stability studies and expiry dating
  • Helps validate lyophilization and drying process effectiveness

Whether you need moisture data for quality control, research dosing accuracy, or stability documentation, Northern Peptide Labs provides fast and reliable Karl Fischer moisture analysis with results included in your Certificate of Analysis.

Get in Touch

Contact Northern Peptide Labs

Reach out with questions about our services, sample submission, or to request a quote. Our team is ready to assist you.

Email

customer.northernpeptide@gmail.com

We respond within one business day

Business Hours

Monday – Friday: 9:00 AM – 5:00 PM EST

Saturday – Sunday: Closed

Location

Northern Peptide Labs

Canada 🍁

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