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Analytical Verification • Lot Lookup

Certificate of Analysis Directory

Search by lot/batch number or compound name to inspect analytical RP-HPLC purity profiles, mass spectrometry verification, and third-party laboratory reports.

Published Batch Reports

Showing all active records
AOD-9604 – 10 mg
LOT: LOT VERIFIED

AOD-9604 – 10 mg

Analytical Reference Standard
HPLC Purity ≥ 99.0%
Specification Analytical Pure
Testing Date Oct 05, 2026
Methodology RP-HPLC • ESI-MS
View COA File
VIP 10 mg
LOT: LOT VERIFIED

VIP 10 mg

Analytical Reference Standard
HPLC Purity ≥ 99.0%
Specification Analytical Pure
Testing Date Oct 03, 2026
Methodology RP-HPLC • ESI-MS
View COA File
Tirzepatide (30MG)
LOT: LOT-30MG

Tirzepatide (30MG)

Variation Reference Standard
HPLC Purity ≥ 99.2%
Specification 30MG
Testing Date Oct 03, 2026
Methodology RP-HPLC • ESI-MS
View COA File
Tirzepatide (60MG)
LOT: LOT-60MG

Tirzepatide (60MG)

Variation Reference Standard
HPLC Purity ≥ 99.2%
Specification 60MG
Testing Date Oct 03, 2026
Methodology RP-HPLC • ESI-MS
View COA File
Thymosin Alpha-1 10 mg
LOT: LOT VERIFIED

Thymosin Alpha-1 10 mg

Analytical Reference Standard
HPLC Purity ≥ 99.0%
Specification Analytical Pure
Testing Date Oct 03, 2026
Methodology RP-HPLC • ESI-MS
View COA File
Semax 10 mg
LOT: LOT VERIFIED

Semax 10 mg

Analytical Reference Standard
HPLC Purity ≥ 99.0%
Specification Analytical Pure
Testing Date Oct 03, 2026
Methodology RP-HPLC • ESI-MS
View COA File
GLP-3 (RT) (10MG)
LOT: RT0004

GLP-3 (RT) (10MG)

Variation Reference Standard
HPLC Purity ≥ 99.2%
Specification 10MG
Testing Date Sep 21, 2026
Methodology RP-HPLC • ESI-MS
View COA File
PACKAGING VERIFICATION

How to Locate Your Batch Code

The batch identification code is laser-etched horizontally across the primary laboratory vial label beside the compound title, formatted as LOT: RTXXXX or AS-XXXX.

SAMPLE LABEL FORMAT LOT: RT0004 ISO 17025 Reference Standard

RESEARCH USE ONLY NOTICE: All Certificates of Analysis and analytical reports provided herein are strictly for laboratory reference, sequence validation, and in vitro experimentation by qualified personnel. Products are not approved by the FDA for clinical, therapeutic, human, or veterinary application.

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