Research Disclaimer: All compounds described are sold exclusively for in-vitro and laboratory research use. Not for unsupervised use. This content does not constitute medical advice.
A Certificate of Analysis (COA) is the foundational quality document for any research compound purchase. It summarizes the analytical testing results that verify a compound's identity, purity, and compliance with specifications. Being able to correctly read and critically evaluate a COA is an essential skill for any researcher procuring compounds for laboratory use — it's the difference between trusting a document and understanding it.
COA Document Structure#
A properly structured COA contains these sections:
Header:
- Laboratory name, address, accreditation numbers (ISO, GLP)
- Report ID / analysis number (key for verification)
- Date of analysis
- Client/supplier name (optional: some labs keep this confidential)
Sample Information:
- Compound name and CAS number
- Batch/lot number
- Physical description (white powder, off-white lyophilized cake)
- Quantity received
Test Results Table: One row per test performed, typically:
| Test | Method | Specification | Result | Pass/Fail |
|---|---|---|---|---|
| Appearance | Visual | White powder | White powder | Pass |
| Purity | HPLC-UV, 214 nm | ≥98.0% | 99.3% | Pass |
| Identity | MS (ESI+) | MW = 1,419.5 ± 0.5 Da | MW = 1,419.6 Da | Pass |
| Endotoxin | LAL | ≤10 EU/mg | 1.2 EU/mg | Pass |
| Moisture | Karl Fischer | ≤5% | 2.8% | Pass |
Signatures:
- Analyst signature and date
- Quality assurance/manager sign-off
Reading Purity Results#
Purity (HPLC area%):
- "99.3%" means 99.3% of UV-absorbing material at the measurement wavelength is the target compound
- The remaining 0.7% is other UV-absorbing material (impurities or degradation products)
- This is relative purity — it assumes the target compound and all impurities have similar UV absorbance
Important nuances:
- 99.3% purity by area% ≠ 99.3% by weight/mass — compounds with different molecular weights and UV extinction coefficients contribute different "signal" per gram
- Low-UV-absorbing impurities may be underrepresented in HPLC-UV purity — HPLC-ELSD or weight-corrected calculations give a truer picture
- For research purposes, HPLC-UV ≥98% is the accepted standard for most applications
What to check in purity testing:
- Measurement wavelength (should be 210–220 nm for broadest detection; 214 nm is standard for peptides)
- Column type (C18 reverse-phase for most peptides and steroids)
- Gradient details (verify method is appropriate for the compound class)
Reading Identity Test Results#
Mass spectrometry (MS) confirmation:
ESI-MS for peptides shows multiply charged ions:
- Look for: Observed m/z value AND corresponding charge state
- Example: "Observed [M+2H]2+: 710.8 m/z; Calculated: 710.8 m/z; Match: Yes"
- This proves the compound has MW of approximately 1,419.5 Da (2 × 710.8 − 2 = 1,419.6)
GC-MS for steroids:
- Retention index compared to reference library
- Fragmentation pattern match (typically expressed as % similarity to NIST library reference)
- ≥95% NIST library similarity = confident identification
What if MS is missing?
- COA shows only HPLC-UV purity without MS identity confirmation
- For common well-established compounds (testosterone enanthate) with standardized HPLC methods and known retention times: may be acceptable
- For peptides: HPLC-UV alone is insufficient; MS confirmation should be required because sequence errors cannot be detected by UV
Reading Endotoxin Results#
LAL (Limulus Amebocyte Lysate) test:
- Measures bacterial endotoxins (lipopolysaccharide, LPS) in EU/mg (Endotoxin Units per milligram)
- USP <85> standard: research injectables typically should be <10 EU/mg
- Result of 1.2 EU/mg is well within specification; result of 8.5 EU/mg is passing but near limit
Why endotoxin matters: 0.1 ng/kg LPS in rodents activates the immune response. Endotoxin contamination in research compounds is the single most common source of false-positive inflammatory results in in vivo studies.
Verifying COA Authenticity#
How to verify a Janoshik COA:
- Note the report ID (alphanumeric code on the COA)
- Go to janoshik.com
- Use the "Verify Report" function
- Enter the report ID
- The live database should return the matching test results
Red flags for fake COAs:
- No report ID present
- Report ID does not return results on lab website
- Date is more than 2 years old (compound may have degraded; batch is likely outdated)
- Purity exactly 99.9% on every compound, every batch (real testing shows variation)
- Lab name is not a real accredited laboratory
Complete Checklist for COA Evaluation#
Before purchasing:
- Third-party lab (not supplier self-tested)
- Report ID present and verifiable on lab website
- Date within 12–24 months
- Compound name + CAS number match expectation
- Batch/lot number listed
- HPLC purity ≥98% (or ≥95% minimum)
- Identity confirmed (MS for peptides; GC-MS or MS for steroids)
- Endotoxin result if injectable use planned
Research Use Only. JuicedPharma does not provide medical advice.
Published by JuicedPharma Research Team · September 2026 · Category: Research Protocols & Science


