Lab Reports

The certificate behind every lot, searchable by batch.

Every vial’s batch number opens its Certificate of Analysis right here: HPLC purity, bacterial endotoxin, sterility, and heavy metals documentation, with identity and lot details matched to the certificate record. Newest lot first, every past lot one search away.

Manufacturer COA + independent re-test
Mytide Lab
Mytide BPC-157 research vial
Verified under
ISO/IEC 17025USP-NFICH Q3DILAC MRA

Certificate of Analysis

Retatrutide

GLP-1 / GIP / Glucagon Agonist

Batch Quadruple-tested report set
Lot numberA1015
Issuing laboratoryUnited Laboratories
ClassificationResearch use only
Test Method / recordReferenceReported resultCertificateStatus
Identity & appearance
Appearance Visual recordReported by labWhite lyophilized powderView report Documented
Identity LC-MS / mass identificationMatches targetRetatrutideView report Documented
Purity & content
Purity HPLC with UV detection coupled with mass spectrometryReported by lab99.52%View report Documented
Net peptide content Issued COA valueReported by lab10.57 mgView report Documented
Microbial & endotoxin
Endotoxin Duplicate analysis · USP <85>Both replicates passReplicate 1: Pass · Replicate 2: PassView report Pass
Sterility Lot-level sterility reviewPassNo growth detectedView report Pass
Microbial screen PCRSeparate test recordNot listed on issued PDFBatch documentationRecord note
Elemental & residual safety
Lead (Pb) ICP-MSBelow acceptance limitPass · below stated limitView report Pass
Cadmium (Cd) ICP-MSBelow acceptance limitPass · below stated limitView report Pass
Mercury (Hg) ICP-MSBelow acceptance limitPass · below stated limitView report Pass
Arsenic (As) ICP-MSBelow acceptance limitPass · below stated limitView report Pass
Residual solvents ICH Q3CSeparate test recordNot listed on issued PDFBatch documentationRecord note
Certificate & report
Purity certificatePer lotMY-RT10View PDF Documented
Endotoxin certificatePer lotMY-RT10View PDF Documented
Sterility certificatePer lotMY-RT10View PDF Documented
Product specification
ClassificationGLP-1 / GIP / Glucagon Agonist
Sequence / compositionTriple GLP-1/GIP/Glucagon Agonist
Molecular weight4731.4 Da
Strength / vial10 mg
FormWhite lyophilized powder
Received dateJul 6, 2026
Report dateJul 24, 2026
Issuing laboratoryUnited Laboratories
Use designationFor laboratory research use only. Not for human consumption.

Identity & appearance

Appearance
White lyophilized powderDocumentedPDF
IdentityLC-MS / mass identification
RetatrutideDocumentedPDF

Purity & content

PurityHPLC analysis
99.52%DocumentedPDF
Net peptide content
10.57 mgDocumentedPDF

Microbial & endotoxin

EndotoxinDuplicate analysis · USP <85>
Both replicates pass PassPDF
SterilityLot-level review
No growth detected PassPDF
Microbial screenPCR
Not listed on issued PDF

Elemental & residual safety

Heavy metalsPb · Cd · Hg · As · ICP-MS
Pass · below stated limits PassPDF
Residual solventsICH Q3C
Not listed on issued PDF

Certificate & lot record

Purity report number
MY-RT10DocumentedPDF
Endotoxin report number
MY-RT10DocumentedPDF
Sterility report number
MY-RT10DocumentedPDF
Issuing laboratory
United LaboratoriesDocumented
Batch match
A1015Documented

Product specification

Classification
GLP-1 / GIP / Glucagon Agonist
Sequence / composition
Triple GLP-1/GIP/Glucagon Agonist
Molecular weight
4731.4 Da
Strength / vial
10 mg
Form
White lyophilized powder
Report date
Jul 24, 2026

Results shown are limited to the documentation currently published for this lot. Open the original laboratory PDFs for the complete methods, specifications, and findings. RESEARCH USE ONLY · Not for human or veterinary use.

cGMP-aligned manufacturing, compliance & testing

ALIGNEDALIGNEDGMP

cGMP · 21 CFR 211

International Organization for StandardizationISO17025ACCREDITED LABORATORY

ISO/IEC 17025 · ILAC MRA

Manufacturing follows cGMP-aligned protocols adapted from 21 CFR Part 211 — documented batch records, controlled-environment monitoring, and lot-by-lot release testing.

Current COA-backed lots are documented around four checkpoints: HPLC purity, bacterial endotoxin, sterility, and heavy metals, with identity and lot details matched to the published certificate.

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