Examples We Test
Representative compounds in this category
Not listed? Use the Other / Not Listed option when submitting — or contact us before shipping to confirm method suitability.
Verifiable Results
Every COA includes a public verification link
Each Certificate of Analysis carries a unique report number and a shareable link. Anyone you provide the COA to can open that link on the Analitika site and confirm the result matches our sealed laboratory record.
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How to submit a sample
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Submit your order
Select your tests, complete the submission form and pay online. Shipping instructions are sent after payment confirmation.
Ship your sample
Send your sample to our Ontario lab. Ship your sample in a sealed vial to our Ontario lab.
Receive your COA
Testing begins within 1 to 3 business days of sample receipt. COA delivered in 3–5 business days via your portal and email.
Common Questions
Frequently asked questions
What does HPLC purity testing detect in a SARM sample?
Reversed-phase HPLC quantifies the relative abundance of each UV-absorbing species in the sample. For a SARM submitted as a single-compound powder or solution, the primary peak area is reported as a percentage of total integrated area — representing chromatographic purity. The analysis also reveals the presence and relative proportion of impurity peaks, degradation products, and unknown components, providing a detailed picture of the sample's analytical composition.
Is purity the same as identity? How do I confirm I have the correct compound?
Purity and identity are distinct measurements. Chromatographic purity tells you what fraction of the detected material corresponds to the primary peak, but cannot by itself confirm the molecular identity of that peak. For identity confirmation, ANALITIKA uses retention-time comparison against a certified reference standard for the declared compound. Where a reference standard is available and a match is confirmed, the COA explicitly states that the primary peak is consistent with the declared compound.
Can ANALITIKA test SARMs in solution form as well as powder?
Yes. SARMs submitted dissolved in research-grade solvents — commonly DMSO, ethanol, or polyethylene glycol — can be analyzed directly. The solvent composition and approximate concentration should be declared at submission so the method can be appropriately adjusted. ANALITIKA's reversed-phase method is compatible with most common research solvents at typical dilution levels; we will advise if a specific matrix presents interference concerns.
What information appears on the COA for a SARM?
The Certificate of Analysis includes the compound name as submitted, the sample reference number, the analytical method applied (HPLC-UV, with the detection wavelength noted), the chromatographic purity result expressed as a percentage, retention time, and a summary of all detected peaks with their relative areas. The COA carries ANALITIKA's standard disclaimer confirming that results are for research-use and research-related purposes only.
Analytical results issued by ANALITIKA COMPOUND TESTING INC. are provided for research-use and research-related purposes only. They describe the sample as received and the analytical methods applied, and constitute analytical data only. ANALITIKA does not determine the safety, suitability for any intended use, or regulatory status of any material tested. These results are not an endorsement, approval, certification, or recommendation of the material for human use or for use in any animal, and must not be presented or relied upon as such. ANALITIKA accepts no responsibility for any use of a tested material beyond the analytical scope of this report.
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