SCALE Performance

SLU-PP-332 Capsules certificate of analysis, lot PL-2610-192

Certificate PL-26-00305 reports the release tests for SLU-PP-332 Capsules lot PL-2610-192: 99.67% purity by reverse-phase HPLC and identity confirmed by LC-MS, tested October 8, 2026. The lot number printed on each unit matches this certificate.

Certificate numberPL-26-00305
Lot numberPL-2610-192
CompoundSLU-PP-332 Capsules 1,000 mcg × 30
Molecular formulaC18H14N2O2
CAS number303760-60-3
Purity (RP-HPLC)99.67%
Identity (LC-MS)Conforms (290.33 Da) · expected 290.32 Da, found 290.33 Da
MethodRP-HPLC (UV 214 nm) + LC-MS
TestedOctober 8, 2026
Retest byOctober 7, 2028
Tested byManufacturer’s in-house laboratory (not an independent third-party test)
ConclusionConforms

Tests run on this lot

TestMethodSpecificationResult
Identity (mass)LC-MS, ESI positiveTheoretical ± 1.0 Da290.33 Da (PASS)
PurityRP-HPLC, UV 254–306 nm, area%≥ 99.0%99.67% (PASS)
Largest impurityRP-HPLC, area%≤ 1.0%0.25% (RT 10.90) (PASS)
Capsule contentContent vs label claim0.9–1.1 mg/cap0.98 mg/cap (PASS)
Bacterial endotoxinLAL, kinetic—— (N/A)
Aerobic count (TAMC)USP <61>< 10 CFU/g< 10 CFU/g (PASS)
Yeast & mold (TYMC)USP <61>< 10 CFU/g< 10 CFU/g (PASS)
E. coliUSP <62>AbsentAbsent (PASS)

What these results mean

HPLC purity is the share of UV-detectable material that elutes as the target compound; it is not the same as net peptide content, which also accounts for water and counter-ions. Identity means the measured mass matched the mass calculated for the compound. A certificate reports only the tests run on this lot; endotoxin, sterility and contaminant panels are not part of standard lot release. How to read a certificate of analysis.

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