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
Is HPLC suitable for analyzing hormone-related research compounds?
Yes. Most hormone analogs and modulators in this category — including aromatase inhibitors, selective estrogen receptor modulators (SERMs), and GnRH analogs — contain aromatic or conjugated structural features well-suited to reversed-phase HPLC with UV detection. ANALITIKA's method separates the primary compound from synthetic impurities, residual precursors, and degradation products, yielding a quantitative chromatographic purity result and a retention-time-based identity comparison against certified reference standards.
What is the difference between purity and potency for these compounds?
Purity, as measured by HPLC, is a chromatographic measurement — it quantifies what fraction of the detected UV-absorbing material corresponds to the declared compound's peak. Potency is a biological or receptor-binding concept that relates to a compound's activity in a biological system. ANALITIKA's testing is strictly analytical: we report chromatographic purity and identity. Biological activity, receptor affinity, and any efficacy endpoint are outside the scope of our analysis.
Can isomers like Enclomiphene and Zuclomiphene be distinguished by HPLC?
Geometric isomers such as the enclomiphene (trans) and zuclomiphene (cis) components of clomiphene can often be separated by reversed-phase HPLC under appropriately optimized gradient conditions. The relative ratio of isomers present in a submission is analytically reportable and may be relevant for research characterization. ANALITIKA will report resolved isomeric composition when chromatographic separation is achieved and reference standards for both isomers are available.
How should peptide-based analogs like Gonadorelin or Kisspeptin-10 be submitted?
Submit as lyophilised powder in a sealed, clearly labeled vial with the compound name and lot reference noted. Peptide-based hormone analogs are analyzed using the same reversed-phase HPLC method applied to other peptide submissions, with UV detection at 214 nm. Contact us if you have questions about sample quantity. Reconstituted solutions may also be submitted — provide the solvent identity and approximate concentration at the time of submission.
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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