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Selank 10mg

Original price was: $29.99.Current price is: $24.99.

(5.0) (55 customer reviews)

Research Studies:

  • Potent ACTH(4-10) analog for investigating melanocortin receptor-mediated neuroplasticity and signaling
  • Facilitates analysis of brain-derived neurotrophic factor expression and trkB receptor activation
  • Supports research on enkephalinase inhibition and subsequent opioid-mediated neuroprotective signaling pathways
  • Enables evaluation of GABAergic system modulation and serotonin metabolic rate in assays

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ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATIONAL AND EDUCATIONAL PURPOSES ONLY. The products offered on this website are intended solely for research and laboratory use. These products are not intended for human or animal consumption. They are not medicines or drugs and have not been evaluated or approved by the FDA to diagnose, treat, cure, or prevent any disease or medical condition. Any form of bodily introduction is strictly prohibited by law.

Description

Selank 10mg is a research-use-only laboratory material supplied for controlled research workflows, compound characterization, and analytical documentation review. It is manufactured under rigorous quality standards to support consistency, traceability, and batch-specific verification for qualified laboratory settings.

Key Product Details

  • Manufactured in accordance with rigorous quality standards to support ≥99% purity, as reflected in batch-specific documentation where available.
  • Every batch is third-party analyzed for identity, assay/potency, and sterility documentation where applicable.
  • Supplied in lyophilized powder form to help preserve stability throughout transport and storage.
  • Produced with lot-level traceability to support research documentation and laboratory recordkeeping.

Research Documentation Context

  • Supports compound characterization in controlled laboratory settings.
  • Provides batch-specific identity and purity documentation for research review.
  • Allows lot-level traceability across laboratory documentation workflows.
  • Supports comparison of product labeling, analytical documentation, and storage information during research planning.
  • Supports analytical review of peptide research materials within a strictly laboratory-focused context.

Specifications and Documentation

  • Certificate of Analysis: Available with batch-specific documentation where applicable.
  • Material Safety Data Sheet: Coming Soon.
  • Handling and Storage Instructions: Coming Soon.
  • Product Form: Lyophilized powder.
  • Purity Specification: ≥99% purity.
  • Intended Use: Laboratory research use only.

Selank 10mg is intended strictly for laboratory research use only. This product is not intended for human or animal consumption, therapeutic use, diagnostic use, clinical use, veterinary use, or as a food, drug, cosmetic, dietary supplement, or household product.

Additional information

CAS No.

129954-34-3

Purity

≥99%

Sequence

Thr-Lys-Pro-Arg-Pro-Gly-Pro

Molecular Formula

C33H57N11O9

Molecular Weight

751.9 g/mol

Synthesis

Solid-phase synthesis

Format

Lyophilized powder

Solubility

Soluble in water or 1% acetic acid

Stability & Storage

Stable for up to 24 months at -20°C. After reconstitution, may be stored at 4°C for up to 4 weeks or at -20°C for up to 6 months.

Applications

Neurological studies, immune system research, cognitive enhancement studies

Appearance

White lyophilized powder

Shipping Conditions

Shipped at ambient temperature; once received, store at -20°C

Regulatory/Compliance

Produced in a facility adhering to cGMP guidelines

Safety Information

Refer to provided MSDS

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Research Procurement Information

Buy Selank Online for Research | COA Procurement Guide

Researchers searching for buy Selank online should evaluate Selank as a research-use-only laboratory material, not a consumer product. For laboratory buyers, the key considerations are compound identity, Selank purity documentation, batch-specific COAs, lot traceability, product labeling, and supplier evaluation. This guide explains how to evaluate Selank 10mg for controlled research procurement through Pure Lab Peptides, with attention to RUO labeling, analytical documentation, identity testing, storage information, and supplier transparency.

Fast Answer: buy Selank online for laboratory research

Researchers can buy Selank online for laboratory research by reviewing RUO labeling, batch-specific COA documentation, purity data, identity information, storage guidance, and supplier transparency before selecting a source. Products discussed in this article are intended for laboratory research use only and are not intended for human or animal consumption.

What Does “Buy Selank Online” Mean in a Research Context?

The phrase buy Selank online is addressed here as laboratory research procurement intent, not personal-use intent. In a compliant RUO context, the searcher is a qualified researcher, laboratory buyer, research institution, or technical procurement team comparing documentation before selecting a research material.

That procurement review should focus on whether Selank is clearly labeled research use only, whether the supplier provides batch-specific documentation, whether the Selank COA supports identity and purity review, and whether lot numbers match across labels and records. FDA IVD labeling materials describe RUO labeling in the specific diagnostic-device context as a way to separate research materials from diagnostic use; that principle is useful as a general documentation boundary, even though peptide procurement must be evaluated under the supplier’s own product documentation and applicable laboratory policies [12] [13] [22].

Selank Research Material Overview

Selank is commonly identified in chemical databases as a peptide with the molecular formula C33H57N11O9, a listed molecular weight of about 751.9 g/mol, and the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro [1]. FDA’s UNII Search Service lists Selank under UNII TS9JR8EP1G, which provides another identity cross-reference for documentation review [2].

From a research-category standpoint, Selank fits the neuroactive or peptide-derivative product category. It is often described in published literature as a synthetic peptide related to tuftsin, the tetrapeptide Thr-Lys-Pro-Arg, which has a long research history in peptide biology [3]. In RUO procurement writing, this literature context should remain neutral: Selank is a laboratory research material whose identity, sequence, molecular mass, purity, and analytical testing are the relevant buying considerations.

Published studies have examined Selank in gene-expression and model-system contexts, including work related to GABAergic gene-expression panels in rat frontal cortex and neuroblastoma IMR-32 cells [4] [5]. Published research context should not be interpreted as cognitive, mood, or wellness guidance for RUO materials.

Why Researchers Search “Buy Selank Online”

Researchers may search buy Selank when they need to evaluate RUO product availability, supplier documentation, product form, lot-level traceability, and analytical support before adding a material to a controlled research workflow. The buying decision should not be based on promotional claims or summaries of biological literature. It should be based on whether the supplier provides documentation that a technical buyer can review.

For Selank research material, that means checking product identity, purity data, Selank identity testing, supplier language, storage information, and batch-specific COA availability. Researchers should also confirm that the supplier avoids dosing, preparation, clinical, diagnostic, veterinary, or personal-use positioning. The procurement question is not “what can this do?” but “is the material documented clearly enough for laboratory research records?”

Research Procurement Checklist for Selank

  • Verify that Selank is labeled for research use only.
  • Review the batch-specific certificate of analysis before procurement.
  • Confirm that the COA includes identity and purity documentation.
  • Check whether HPLC, LC-MS, mass spectrometry, or another analytical method is listed.
  • Compare the product name, lot number, and documentation for consistency.
  • Assess whether the supplier avoids dosing, therapeutic, clinical, veterinary, or personal-use claims.
  • Document storage and handling information in laboratory records.
  • Evaluate whether lyophilized powder form matches the research workflow.
  • Confirm that the product is not marketed for human or animal consumption.

Selank Quality Signals to Review Before Buying Online

When researchers evaluate where to buy Selank online for laboratory research, the strongest quality signals are documentation-based: RUO labeling, Selank COA access, purity data, identity confirmation, traceable lot information, and supplier language that stays within research-use-only boundaries.

Evaluation Area What Researchers Should Review Why It Matters for RUO Procurement
RUO labeling Confirm the product is clearly labeled for research use only Helps separate research procurement from human-use positioning
COA availability Review batch-specific certificate of analysis Supports lot-level documentation and quality review
Purity data Look for analytical support for the stated purity Helps evaluate material consistency
Identity testing Review HPLC, LC-MS, mass spectrometry, or related identity data where available Helps confirm the material matches the listed compound
Lot traceability Match lot numbers across product and documentation Supports research recordkeeping
Product form Confirm whether the material is supplied as lyophilized powder or another documented form Supports laboratory planning
Storage information Review storage and handling documentation Helps maintain material integrity in laboratory settings
Supplier language Confirm the supplier avoids dosing, therapeutic, or personal-use claims Supports research-use-only positioning

COA, Purity, and Identity Documentation

A strong Selank supplier documentation package should let a researcher connect the listed compound name, lot number, product form, purity percentage, analytical method, and identity data into one consistent record. A purity percentage alone does not establish complete compound identity; researchers should evaluate purity, identity, method, lot number, and documentation together.

Laboratory quality frameworks such as ISO/IEC 17025 emphasize competence and consistent operation in testing and calibration laboratories, while ICH Q2(R2) and Q14 describe analytical validation and analytical procedure development principles in regulated analytical contexts [14] [15] [16]. For peptide characterization, HPLC is widely used for peptide analysis and purification, while mass spectrometry and LC-MS approaches support mass confirmation, identity assessment, and impurity review [17] [18] [19] [20] [21].

For Selank purity documentation, researchers should review whether the COA identifies the compound, lists the lot number, states the analytical method, reports purity, and provides identity support. For Selank supplier documentation, the most useful records are batch-specific rather than generic.

flowchart TD A[Receive product and COA] --> B{RUO labeling present?} B -- No --> C[Flag procurement gap] B -- Yes --> D{Lot number matches across label and COA?} D -- No --> E[Request batch-specific documentation] D -- Yes --> F{Identity supported by analytical method?} F -- No --> G[Request HPLC, LC-MS, or equivalent] F -- Yes --> H[Proceed to laboratory documentation and storage]

Research Literature Context

Published literature discusses Selank in several research settings, including peptide identity, tuftsin-related peptide context, gene-expression models, enzymatic degradation models, and limited human study settings outside the scope of RUO product use. The literature should be treated as scientific context, not as instructions for use of a research-use-only material.

Volkova and colleagues examined changes in gene-expression panels after Selank exposure in a rat model, while Filatova and colleagues examined GABA, Selank, and olanzapine in an IMR-32 cell model [4] [5]. Kost and colleagues reported work on Selank and Semax in relation to enkephalin-degrading enzymes, and Zolotarev and colleagues described tritium-labeled peptide approaches for biodegradation studies [6] [7]. Other literature includes preclinical model studies and functional-connectivity research, but those publications do not convert RUO materials into clinical, diagnostic, or personal-use products [8] [9] [10].

Published clinical literature should not be interpreted as use guidance for RUO materials. The existence of clinical literature in a different context does not alter the intended use, labeling, documentation needs, or procurement review standards for a Selank research-use-only material [11].

Evidence Landscape

Research Area What Literature Examines Evidence Type RUO Interpretation
Compound identity Molecular structure, sequence, formula, or classification Database / analytical Supports identification, not product-use claims
Peptide-derivative context Tuftsin-related peptide literature and model-specific research areas Review / in vitro / preclinical Useful for research context, not therapeutic claims
Analytical testing Purity, identity, and batch verification HPLC / LC-MS / mass spectrometry / COA Supports documentation review
Storage and stability Material form and handling considerations Laboratory documentation Supports research workflow planning

Claim Boundary Table

Research-Safe Statement Why It Is Acceptable Non-Compliant Version to Avoid
“Selank is discussed in published research related to peptide-derivative and neuropeptide model contexts.” Describes literature context without making a product claim “Selank helps with a human outcome.”
“Researchers should review COA and identity data before procurement.” Focuses on documentation and quality review “Users should buy Selank for results.”
“Pure Lab Peptides supplies Selank as a research-use-only material.” Clarifies intended use “Pure Lab Peptides supplies Selank for therapy.”
“The phrase buy Selank online is addressed as research procurement intent.” Qualifies commercial search intent “Buy Selank online for personal use.”
“Selank identity testing should be reviewed alongside purity documentation.” Connects procurement to analytical documentation “Purity alone proves how Selank should be used.”

How Pure Lab Peptides Presents Selank

Pure Lab Peptides presents Selank 10mg as a research-use-only material with a ≥99% purity claim, lyophilized powder form, batch-specific COA availability, product documentation, storage and handling information, lot-level traceability, and supplier transparency. These are procurement and documentation signals for qualified research buyers, not personal-use claims.

Review the Pure Lab Peptides Selank research-use-only product page for RUO labeling, product details, purity information, and batch-specific documentation. Researchers comparing broader peptide options can also review the Pure Lab Peptides research peptide collection, the Pure Lab Peptides blog archive, and the shipping and returns information for procurement planning.

Common Misunderstandings About Buying Selank Online

Misunderstanding: “Buy Selank online” means personal use

Buy Selank online should not be interpreted as personal-use guidance on this page. The phrase is addressed as laboratory procurement intent for qualified researchers reviewing RUO labeling, documentation, purity data, identity information, and supplier transparency.

Misunderstanding: Published literature equals product-use guidance

Published literature can help researchers understand why a compound appears in scientific databases and model-system publications. It does not explain how to use an RUO material, and it should not be converted into clinical, consumer, wellness, or veterinary positioning.

Misunderstanding: Purity percentage alone proves identity

A Selank purity documentation claim is useful only when reviewed with identity testing, method information, lot number, product name, and batch-specific records. A single percentage does not replace HPLC, LC-MS, mass spectrometry, or equivalent analytical support.

Misunderstanding: COA documentation does not need to be batch-specific

For research procurement, a batch-specific Selank COA is more useful than generic quality language. The lot number on the COA should match the product label or procurement record so the laboratory can connect documentation to the material received.

Misunderstanding: RUO labeling supports human or animal use

RUO labeling supports research-use-only positioning. It does not support human consumption, animal consumption, clinical use, diagnostic use, veterinary use, or personal experimentation. Supplier language should remain consistent with research procurement.

Misunderstanding: Supplier claims can replace analytical documentation

Supplier transparency means providing documentation that researchers can evaluate. Marketing statements should not replace Selank identity testing, purity documentation, lot traceability, storage information, and batch-specific COA review.

FAQs About Buying Selank Online for Research

Where can researchers buy Selank online for laboratory research?

Researchers can buy Selank online for laboratory research from an RUO supplier that provides clear product labeling, purity documentation, identity information, batch-specific COA access, product form details, and lot-level traceability. Pure Lab Peptides provides Selank 10mg product information for qualified research procurement review.

What should researchers check before buying Selank online?

Before buying Selank online, researchers should check RUO labeling, the Selank COA, the stated purity, identity testing, lot number consistency, storage guidance, supplier language, and product form. The supplier should avoid human-use, animal-use, clinical, diagnostic, and personal-use positioning.

Why does a COA matter when buying Selank?

A COA matters when buying Selank because it connects the research material to batch-specific quality documentation. Researchers should review compound name, lot number, purity data, analytical method, identity support, test date, product form, and documentation consistency before adding the material to laboratory records.

Is Selank intended for human or animal consumption?

Selank discussed here is not intended for human or animal consumption. This article addresses Selank research-use-only procurement, documentation review, analytical testing, purity records, identity confirmation, and supplier transparency for qualified laboratory contexts only.

What does research use only mean for Selank?

Research use only for Selank means the material is positioned for controlled laboratory research and documentation review. It is not positioned for clinical use, diagnostic use, veterinary use, personal use, consumer supplementation, or wellness purposes.

How should published literature about Selank be interpreted?

Published literature about Selank should be interpreted as scientific context for researchers, not as product-use guidance. Research publications may discuss peptide identity, model systems, gene-expression experiments, or analytical methods, but RUO procurement still depends on labeling, COA review, purity documentation, and identity testing.

Next Steps

Qualified researchers evaluating Selank should review product labeling, COA status, identity documentation, storage information, and supplier transparency. Review the Selank product page for RUO labeling, purity information, and available batch-specific documentation.

References

  1. National Center for Biotechnology Information. “Selank.” PubChem Compound Summary. 2026. https://pubchem.ncbi.nlm.nih.gov/compound/Selank
  2. U.S. Food and Drug Administration. “SELANK: UNII TS9JR8EP1G.” UNII Search Service. 2026. https://precision.fda.gov/uniisearch/srs/unii/ts9jr8ep1g
  3. Fridkin M, Najjar VA. “Tuftsin: its chemistry, biology, and clinical potential.” Critical Reviews in Biochemistry and Molecular Biology. 1989;24(1):1-40. https://pubmed.ncbi.nlm.nih.gov/2667894/
  4. Volkova A, Shadrina M, Kolomin T, et al. “Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission.” Frontiers in Pharmacology. 2016;7:31. https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2016.00031/full
  5. Filatova E, Shadrina M, Slominsky P, et al. “GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells.” Frontiers in Pharmacology. 2017;8:89. https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00089/full
  6. Kost NV, Sokolov OY, Gabaeva MV, et al. “Semax and selank inhibit the enkephalin-degrading enzymes from human serum.” Bioorganicheskaia Khimiia. 2001;27(3):180-183. https://pubmed.ncbi.nlm.nih.gov/11443939/
  7. Zolotarev IA, Dadaian AK, Dolotov OV, et al. “Evenly tritium-labeled peptides and their in vivo and in vitro biodegradation.” Bioorganicheskaia Khimiia. 2006;32(2):183-191. https://pubmed.ncbi.nlm.nih.gov/16637290/
  8. Kasian A, Kolomin T, Andreeva L, et al. “Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats.” Behavioural Neurology. 2017;2017:5091027. https://doi.org/10.1155/2017/5091027
  9. Kolik LG, Nadorova AV, Antipova TA, et al. “Selank, Peptide Analogue of Tuftsin, Protects Against Ethanol-Induced Memory Impairment by Regulating of BDNF Content in the Hippocampus and Prefrontal Cortex in Rats.” Bulletin of Experimental Biology and Medicine. 2019;167:641-644. https://doi.org/10.1007/s10517-019-04588-9
  10. Panikratova YR, Lebedeva IS, Sokolov OY, et al. “Functional Connectomic Approach to Studying Selank and Semax Effects.” Doklady Biological Sciences. 2020;490(1):9-11. https://pubmed.ncbi.nlm.nih.gov/32342318/
  11. Zozulia AA, Neznamov GG, Siuniakov TS, et al. “Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia.” Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova. 2008;108(4):38-48. https://pubmed.ncbi.nlm.nih.gov/18454096/
  12. Electronic Code of Federal Regulations. “21 CFR 809.10 – Labeling for in vitro diagnostic products.” eCFR. 2026. https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-809/subpart-B/section-809.10
  13. U.S. Food and Drug Administration. “Distribution of In Vitro Diagnostic Products Labeled for Research Use Only or Investigational Use Only.” FDA Guidance Document. 2013, updated 2018. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/distribution-in-vitro-diagnostic-products-labeled-research-use-only-or-investigational-use-only
  14. International Organization for Standardization. “ISO/IEC 17025:2017 General requirements for the competence of testing and calibration laboratories.” ISO Standard. 2017. https://www.iso.org/standard/66912.html
  15. U.S. Food and Drug Administration. “Q2(R2) Validation of Analytical Procedures.” FDA Guidance Document. 2024. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/q2r2-validation-analytical-procedures
  16. U.S. Food and Drug Administration. “Q14 Analytical Procedure Development.” FDA Guidance Document. 2024. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/q14-analytical-procedure-development
  17. Mant CT, Chen Y, Yan Z, et al. “HPLC analysis and purification of peptides.” Methods in Molecular Biology. 2007;386:3-55. https://pubmed.ncbi.nlm.nih.gov/18604941/
  18. Prabhala BK, Mirza O, Hojrup P, Hansen PR. “Characterization of Synthetic Peptides by Mass Spectrometry.” Methods in Molecular Biology. 2015;1348:77-82. https://pubmed.ncbi.nlm.nih.gov/26424265/
  19. Zeng K, Geerlof-Vidavsky I, Gucinski A, Jiang X, Boyne MT 2nd. “Liquid Chromatography-High Resolution Mass Spectrometry for Peptide Drug Quality Control.” AAPS Journal. 2015;17(3):643-651. https://pubmed.ncbi.nlm.nih.gov/25716148/
  20. Lian Z, Xu Y, Chen X, et al. “Characterization of Synthetic Peptide Therapeutics Using Liquid Chromatography-Mass Spectrometry: Challenges, Solutions, Pitfalls, and Future Perspectives.” Journal of the American Society for Mass Spectrometry. 2021;32(8):1852-1860. https://pubmed.ncbi.nlm.nih.gov/34110145/
  21. Li M, Josephs RD, Daireaux A, Choteau T, Westwood S, Wielgosz RI. “Impurity determination for human C-peptide by liquid chromatography-high resolution tandem mass spectrometry.” Analytical and Bioanalytical Chemistry. 2018;410(20):5059-5070. https://pubmed.ncbi.nlm.nih.gov/29862433/
  22. U.S. Food and Drug Administration. “In Vitro Diagnostic Device Labeling Requirements.” FDA Medical Devices. 2023. https://www.fda.gov/medical-devices/device-labeling/in-vitro-diagnostic-device-labeling-requirements

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