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Retatrutide (10mg) - Box of 10 Vials
RT10

Retatrutide 10mg – Box of 10 Research Vials

Tested batch: EP-260514-RE10

Retatrutide is a triple hormone receptor agonist peptide. Each box contains 10 vials of lyophilized powder, with 10mg per vial. This peptide is supplied as a research compound for laboratory use only.

Specifications: SKU RT10 · 10 vials of lyophilised powder per box · 10mg per vial · measured net content 11.76 mg. Testing: four Kovera Labs reports for batch EP-260514-RE10: RP-HPLC purity 99.337% with LC-MS identity, endotoxin < 0.20 EU/mL, heavy metals and sterility – see the certificates below. For laboratory research use only; not for human consumption.

$544.50

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Research Use Only

This product is strictly intended for laboratory research use only. Not for human consumption. All products sold are for research purposes and should only be handled by qualified professionals in a controlled laboratory environment.

Retatrutide (10mg): Kovera Labs testing overview

Tested batch: EP-260514-RE10 · 4 published certificates. Report library updated .

Batch EP-260514-RE10 – four Kovera Labs reports. Purity and identity: RP-HPLC purity 99.337%, net content 11.76 mg, LC-MS identity: EP-3 (R) (KVR-2026-D3DB01, 29 June 2026). Endotoxin: < 0.20 EU/mL (ENDO-KVR-2026-D3DB01). Heavy metals: lead < 0.5, arsenic < 0.15, cadmium < 0.05 and mercury < 0.3 ppm (HM-KVR-2026-D3DB01). Sterility: no bacterial growth (aerobic and anaerobic) and no fungi or yeast detected after a 2-day incubation (RSTER-KVR-2026-D3DB01). Each certificate links to its Kovera Labs verification record, and the product image shows the same batch reference. For laboratory research use only.

Tests and results printed on the supplied Kovera Labs certificates
TestReported resultReport IDReport date
Purity and Identity (COA)Purity: 99.337 %; Net content: 11.76 mg; Identity confirmation: EP-3 (R)KVR-2026-D3DB0129 June 2026
EndotoxinEndotoxin: < 0.20 EU/mLENDO-KVR-2026-D3DB0130 May 2026
Heavy MetalsLead: < 0.5 ppm; Arsenic: < 0.15 ppm; Cadmium: < 0.05 ppm; Mercury: < 0.3 ppmHM-KVR-2026-D3DB0131 May 2026
Sterility testingBacteria (aerobic/anaerobic): No Growth; Fungi / yeast: Not Detected; Incubation period: 2 daysRSTER-KVR-2026-D3DB0130 May 2026

Read how to interpret and verify a Kovera Labs report or browse our testing standards and report directory.

Purity and Identity (COA)

Report KVR-2026-D3DB01 · 29 June 2026

Kovera Labs Purity and Identity (COA) certificate for Retatrutide (10mg), tested, KVR-2026-D3DB01 Verify this certificate on Kovera Labs

Opens the issuing laboratory’s verification record. Match the report ID, sample and batch.

Read report results as text
Reported testResultStated criterionMethod, where stated
Purity99.337 %—RP-HPLC
Net content11.76 mg——
Identity confirmationEP-3 (R)—LC-MS
Endotoxin screenPASS——
Microbial sterility screenNo Growth——
Arsenic (As) screeningNegative——
Cadmium (Cd) screeningNegative——
Lead (Pb) screeningNegative——
Mercury (Hg) screeningNegative——

Endotoxin

Report ENDO-KVR-2026-D3DB01 · 30 May 2026

Kovera Labs Endotoxin certificate for Retatrutide (10mg), tested, ENDO-KVR-2026-D3DB01 Verify this certificate on Kovera Labs

Opens the issuing laboratory’s verification record. Match the report ID, sample and batch.

Read report results as text
Reported testResultStated criterionMethod, where stated
Endotoxin< 0.20 EU/mL≤ 0.5—
Final determinationPASS——

Heavy Metals

Report HM-KVR-2026-D3DB01 · 31 May 2026

Kovera Labs Heavy Metals certificate for Retatrutide (10mg), tested, HM-KVR-2026-D3DB01 Verify this certificate on Kovera Labs

Opens the issuing laboratory’s verification record. Match the report ID, sample and batch.

Read report results as text
Reported testResultStated criterionMethod, where stated
Lead< 0.5 ppm≤ 10ICP-MS
Arsenic< 0.15 ppm≤ 1.5ICP-MS
Cadmium< 0.05 ppm≤ 0.5ICP-MS
Mercury< 0.3 ppm≤ 3ICP-MS

Sterility testing

Report RSTER-KVR-2026-D3DB01 · 30 May 2026

Kovera Labs Sterility testing certificate for Retatrutide (10mg), tested, RSTER-KVR-2026-D3DB01 Verify this certificate on Kovera Labs

Opens the issuing laboratory’s verification record. Match the report ID, sample and batch.

Read report results as text
Reported testResultStated criterionMethod, where stated
Bacteria (aerobic/anaerobic)No Growth——
Fungi / yeastNot Detected——
Incubation period2 days——
Temperature30-35C——
Final determinationSAMPLE PASSES STERILITY SCREEN——

Research evidence

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