Understand the source comparison
LIPO-C Real vs Fake: Visual and Chemical Comparison
Reconstitution clarity Clear amber solution within 90 seconds, zero particulate matter Cloudy, incomplete dissolution, visible sediment or off-white particles Cloudiness indicates impure precursors or incorrect amino acid ratios. Immediate rejection criterion
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This page preserves a source comparison for education. It does not add a rating, recommendation or clinical judgment.
- Reconstitution clarity
- Clear amber solution within 90 seconds, zero particulate matter
- Cloudy, incomplete dissolution, visible sediment or off-white particles
- Cloudiness indicates impure precursors or incorrect amino acid ratios. Immediate rejection criterion
- pH stability (15 min post-mix)
- 5.5–6.5 on standard pH strips
- <5.0 or >7.0, indicating poor buffering or degradation byproducts
- pH drift is the clearest chemical fingerprint of illicit manufacturing. Authentic formulations maintain narrow range
- Third-party COA
- Batch-specific HPLC from ISO 17025-accredited lab, ≥98% purity
- No COA, generic document, or visibly altered report
- Lack of verifiable third-party testing is the single strongest indicator of grey-market sourcing
- Storage temperature at delivery
- Arrives cold (2–8°C) with gel packs and temperature indicators
- Room temperature, no cold chain packaging
- Temperature excursion above 8°C for >48 hours denatures amino acids irreversibly. Renders product ineffective
- Supplier transparency
- Provides synthesis facility name, FDA registration number, batch traceability
- Vague claims ('FDA-approved facility'), no specific facility details
- Legitimate suppliers disclose manufacturing origin without hesitation. Vagueness signals grey-market operations
- Solution colour intensity
- Deep amber hue from cyanocobalamin at therapeutic concentration
- Pale yellow or colourless, indicating B12 deficiency or substitution
- Colour intensity correlates directly with B12 content. Pale solutions fail potency standards