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Tesamorelin 5mg

$69.99

(5.0) (55 customer reviews)

Research Studies:

  • Potent GHRH-analog for stimulating pulsatile growth hormone secretion in somatotroph models
  • Facilitates analysis of GH-mediated lipolytic signaling and visceral adipose metabolic flux
  • Supports investigation into insulin-like growth factor-1 induction and systemic anabolic pathways
  • Useful for probing hypothalamic-pituitary-somatotropic axis regulation in cellular research 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

Tesamorelin 5mg 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.

Tesamorelin 5mg 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.

901758-09-6

Purity

≥99%

Sequence

Trans-3-Hexenoyl-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2

Molecular Formula

C221H366N72O67S

Molecular Weight

5135.89 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

Growth hormone secretion studies, metabolic regulation research, obesity therapy research

Appearance

White lyophilized powder

Shipping Conditions

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

Regulatory/Compliance

Manufactured in a facility that adheres to cGMP guidelines

Safety Information

Refer to provided MSDS

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Research Procurement Information

Buy Tesamorelin Online for RUO Research | COA Guide

Researchers searching for buy Tesamorelin online should evaluate Tesamorelin as a research-use-only laboratory material, not a consumer product. For laboratory buyers, the key considerations are compound identity, purity documentation, batch-specific COAs, lot traceability, product labeling, and storage information. This guide explains how to evaluate Tesamorelin for controlled research procurement through Pure Lab Peptides while keeping the discussion limited to documentation, analytical review, and supplier evaluation.

Fast Answer: buy Tesamorelin online for laboratory research

Researchers can buy Tesamorelin 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 Tesamorelin Online” Mean in a Research Context?

The phrase “buy Tesamorelin online” is addressed here as laboratory research procurement intent, not personal-use intent. Qualified researchers, laboratory buyers, research institutions, and technical procurement teams use this type of search to compare RUO labeling, analytical documentation, purity information, compound identity support, and supplier transparency.

In a research procurement setting, the question is not how a compound is used in a person or animal. The question is whether the Tesamorelin research material is documented clearly enough for laboratory records. That includes checking the product name, lot number, batch-specific certificate of analysis, analytical method, storage information, and consistency between product page language and documentation.

RUO language also matters because intended-use statements must be consistent with supplier claims. FDA guidance for RUO and IUO in vitro diagnostic products illustrates the broader compliance principle that research labeling should align with research positioning, while 21 CFR 809.10 describes labeling language for certain RUO products in that specific regulatory context [1] [2]. For Tesamorelin research-use-only procurement, the practical takeaway is straightforward: supplier language should avoid dosing, therapeutic, diagnostic, veterinary, or personal-use framing.

Tesamorelin Research Material Overview

Tesamorelin is identified in scientific databases as a peptide compound. PubChem lists Tesamorelin with the molecular formula C221H366N72O67S and provides a structured chemical record for compound identity review [3]. FDA labeling for the regulated medicine describes tesamorelin acetate as a synthetic growth hormone-releasing factor analog made from the 44-amino-acid sequence of human growth hormone-releasing factor with an N-terminal hexenoyl modification [4]. That regulated-medicine literature is useful for compound identity context only; it is not use guidance for RUO materials.

The IUPHAR/BPS Guide to Pharmacology lists tesamorelin as a peptide and describes it as a stabilized synthetic peptide analog of hypothalamic GHRH [5]. ChEMBL and DrugBank also maintain database records for Tesamorelin, which can help laboratory teams compare identifiers, names, and classification language during identity review [6] [7].

In research-category terms, Tesamorelin belongs in the GHRH pathway and peptide analog category. NCBI Gene identifies GHRHR as the gene encoding the growth hormone-releasing hormone receptor, and UniProt provides a protein record for the human GHRH receptor [8] [9]. These pathway references support neutral research classification. They do not create product-use instructions, therapeutic claims, or personal-use guidance.

Why Researchers Search “Buy Tesamorelin Online”

Researchers search “buy Tesamorelin online” to locate RUO product availability and compare documentation standards. A laboratory procurement team may need Tesamorelin supplier documentation before approving a purchase request, logging a material into an inventory system, or matching a received vial to a batch-specific COA.

The secondary phrase buy Tesamorelin should be interpreted in the same way: as procurement shorthand for research-use-only sourcing. A qualified buyer should review whether the supplier provides a Tesamorelin COA, Tesamorelin purity documentation, Tesamorelin identity testing information, lot-level traceability, product form details, storage language, and clear RUO labeling.

Online availability alone is not a quality signal. A research buyer should evaluate whether the supplier documents the material in a way that supports laboratory recordkeeping and avoids human-use or animal-use positioning.

Research Procurement Checklist for Tesamorelin

  • Verify that Tesamorelin 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, diagnostic, 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.

Tesamorelin Quality Signals to Review Before Buying Online

Researchers evaluating buy Tesamorelin online for laboratory research should focus on documentation rather than promotional language. A strong procurement review combines label review, COA review, analytical method review, and lot matching. Analytical method validation principles are commonly discussed through ICH Q2(R2), while ICH Q14 describes development and lifecycle concepts for analytical procedures [10] [11].

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 Tesamorelin COA should be reviewed as a batch-level document. Researchers should look for the compound name, lot number, product form, test date, purity percentage, analytical method, identity confirmation, and any chromatogram or mass data included in the supplier documentation. FDA bioanalytical guidance emphasizes that documented methods, validation summaries, and analytical records are central to reliable analytical reporting in regulated bioanalytical contexts [12].

A purity percentage alone does not establish complete compound identity; researchers should evaluate purity, identity, method, lot number, and documentation together. HPLC is widely used for peptide analysis and purification, and LC-HRMS has been discussed as a quality-control approach for peptide-related impurity and identity work [13] [14]. Peptide impurity literature also shows why related substances, sequence variants, and degradation products can matter in peptide quality review [15].

For laboratory procurement, method context matters. A chromatographic purity value can help evaluate consistency, while mass spectrometry or LC-MS information can support molecular identity. Two-dimensional chromatographic approaches have also been discussed for peak-purity assessment in pharmaceutical peptide methods [16]. Storage documentation should be reviewed alongside analytical documentation because stability guidance treats temperature, humidity, light, and time as relevant quality variables [17]. WHO storage and transport guidance similarly emphasizes documented control of storage and distribution conditions for time- and temperature-sensitive materials [18].

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 Tesamorelin in several contexts, including compound classification, GHRH pathway research, database annotation, analytical detection, and clinical literature outside the scope of RUO product use. Wang and Tomlinson reviewed Tesamorelin as a human growth hormone-releasing factor analog in 2009, while later reviews summarized clinical literature involving regulated medicine contexts [19] [20].

Those publications are not instructions for RUO material handling. Published clinical literature should not be interpreted as use guidance for RUO materials. Bedimo and colleagues reviewed growth hormone and Tesamorelin literature in HIV-associated lipodystrophy, and Falutz and colleagues published pooled clinical-trial analysis of Tesamorelin as TH9507 [21] [22]. For this procurement guide, those sources are cited only to establish that human clinical literature exists outside the scope of RUO product use.

Other research has examined GHRH analog biology, receptor context, and analytical detection. Stanley and colleagues evaluated a GHRH analog in a human study context, while Knoop and colleagues described LC-HRMS/MS identification of growth hormone-releasing hormones in plasma [23] [24]. More recent analytical literature has addressed chromatographic-mass spectrometric analysis of peptidic analytes and nano-LC quadrupole/orbitrap MS analysis of GHRH analogs including tesamorelin [25] [26].

Pathway relevance in published literature does not establish product-use guidance for RUO materials. The safe interpretation is documentation-focused: published literature can inform compound classification, analytical method awareness, and research context, but it should not be converted into dosing, administration, therapeutic, diagnostic, wellness, or consumer claims.

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
Pathway or category context GHRH receptor pathway and peptide analog research area Review / database / analytical 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
“Tesamorelin is discussed in published research related to GHRH pathway literature.” Describes literature context without making a product claim “Tesamorelin helps with human outcomes.”
“Researchers should review COA and identity data before procurement.” Focuses on documentation and quality review “Users should buy Tesamorelin for results.”
“Pure Lab Peptides supplies Tesamorelin as a research-use-only material.” Clarifies intended use “Pure Lab Peptides supplies Tesamorelin for therapy.”
“The phrase buy Tesamorelin online is addressed as research procurement intent.” Qualifies commercial search intent “Buy Tesamorelin online for personal use.”
“Tesamorelin identity testing should be reviewed with lot-specific documentation.” Connects identity review to procurement records “Supplier claims can replace analytical documentation.”

How Pure Lab Peptides Presents Tesamorelin

Pure Lab Peptides presents Tesamorelin 5mg as a research-use-only material for qualified laboratory procurement. The fixed product information for this article identifies the product form as lyophilized powder, the purity claim as ≥99% purity, and the COA status as available. Researchers should review the batch-specific COA, product page documentation, purity information, storage and handling documentation, and lot-level traceability before completing procurement records.

Review the Pure Lab Peptides Tesamorelin research-use-only product details for RUO labeling, product details, purity information, and batch-specific documentation. Research teams comparing suppliers may also review the broader research peptide collection to evaluate documentation consistency across RUO materials.

Common Misunderstandings About Buying Tesamorelin Online

Misunderstanding: “Buy Tesamorelin online” means personal use

Buy Tesamorelin 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, lot traceability, and supplier transparency.

Misunderstanding: Published literature equals product-use guidance

Published literature can help identify research categories, analytical methods, compound names, and database identifiers. It should not be converted into product-use guidance for RUO materials. Published clinical literature should not be interpreted as use guidance for RUO materials.

Misunderstanding: Purity percentage alone proves identity

A stated purity percentage is only one part of a documentation review. Researchers should review Tesamorelin purity documentation together with identity data, method information, lot number, test date, product name consistency, and COA traceability.

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

For research procurement, batch-specific documentation is important because the COA should correspond to the material received. Researchers should match the lot number on the label, product record, and Tesamorelin COA before filing laboratory documentation.

Misunderstanding: RUO labeling supports human or animal use

RUO labeling does not support human-use, animal-use, clinical, diagnostic, veterinary, or consumer positioning. A Tesamorelin research-use-only listing should remain limited to research procurement, laboratory documentation, supplier evaluation, and controlled research recordkeeping.

Misunderstanding: Supplier claims can replace analytical documentation

Supplier language should be supported by documentation. Research teams should prioritize batch-specific COAs, identity testing, purity information, lot traceability, and storage documentation over broad promotional claims. Tesamorelin supplier documentation should be specific enough for procurement records.

FAQs About Buying Tesamorelin Online for Research

Where can researchers buy Tesamorelin online for laboratory research?

Researchers can buy Tesamorelin online for laboratory research by reviewing RUO suppliers that provide clear product labeling, batch-specific COA documentation, purity information, identity support, storage details, and lot traceability. Pure Lab Peptides provides a Tesamorelin 5mg product page for researchers evaluating documentation before procurement.

What should researchers check before buying Tesamorelin online?

Before buying Tesamorelin online, researchers should check RUO labeling, product form, lot number consistency, batch-specific COA availability, purity documentation, analytical method information, identity testing, and supplier language. The supplier should avoid dosing, therapeutic, clinical, veterinary, diagnostic, or personal-use positioning.

Why does a COA matter when buying Tesamorelin?

A COA matters when buying Tesamorelin because it supports batch-level documentation. Researchers should review whether the COA lists the compound name, lot number, test date, purity value, analytical method, and identity confirmation. A COA should be evaluated with the product label and procurement record.

Is Tesamorelin intended for human or animal consumption?

Tesamorelin discussed on this page is not intended for human or animal consumption. This article addresses Tesamorelin as a research-use-only laboratory material. It does not provide dosing, preparation, administration, clinical, veterinary, diagnostic, therapeutic, wellness, or personal-use guidance.

What does research use only mean for Tesamorelin?

Research use only means Tesamorelin is positioned as a laboratory research material for qualified researchers and technical procurement teams. The procurement review should focus on labeling, COA documentation, purity data, identity testing, lot traceability, storage information, and supplier transparency.

How should published literature about Tesamorelin be interpreted?

Published literature about Tesamorelin should be interpreted as scientific context, not product-use guidance. Database records and analytical publications can support identity and method awareness. Clinical literature, where it exists, should not be applied to RUO materials or converted into product claims.

Next Steps

Qualified researchers evaluating Tesamorelin should review product labeling, COA status, identity documentation, storage information, and supplier transparency. Review the Tesamorelin product page for RUO labeling, purity information, and available batch-specific documentation before selecting any research-use-only material.

References

  1. 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. fda.gov/regulatory-information/search-fda-guidance-documents/distribution-in-vitro-diagnostic-products-labeled-research-use-only-or-investigational-use-only
  2. Electronic Code of Federal Regulations. “21 CFR 809.10 – Labeling for in vitro diagnostic products.” eCFR. Current. ecfr.gov/current/title-21/chapter-I/subchapter-H/part-809/subpart-B/section-809.10
  3. National Center for Biotechnology Information. “Tesamorelin.” PubChem Compound CID 16137828. pubchem.ncbi.nlm.nih.gov/compound/Tesamorelin
  4. U.S. Food and Drug Administration. “Full Prescribing Information: EGRIFTA WR (tesamorelin).” FDA Drug Label. 2025. accessdata.fda.gov/drugsatfda_docs/label/2025/022505s020lbl.pdf
  5. IUPHAR/BPS Guide to Pharmacology. “Tesamorelin.” IUPHAR/BPS Guide to Pharmacology Ligand Database. guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=6959&tab=structure
  6. European Bioinformatics Institute. “TESAMORELIN (CHEMBL1237026).” ChEMBL. ebi.ac.uk/chembl/explore/compound/CHEMBL1237026
  7. DrugBank. “Tesamorelin DB08869.” DrugBank Online. go.drugbank.com/drugs/DB08869
  8. National Center for Biotechnology Information. “GHRHR growth hormone releasing hormone receptor.” NCBI Gene. ncbi.nlm.nih.gov/gene/2692
  9. UniProt Consortium. “Q02643 – GHRHR_HUMAN.” UniProtKB. uniprot.org/uniprotkb/Q02643/entry
  10. International Council for Harmonisation. “Q2(R2) Validation of Analytical Procedures.” ICH Harmonised Guideline. 2023. database.ich.org/sites/default/files/ICH_Q2%28R2%29_Guideline_2023_1130.pdf
  11. International Council for Harmonisation. “Q14 Analytical Procedure Development.” ICH Harmonised Guideline. 2023, error correction 2025. database.ich.org/sites/default/files/ICH_Q14_Guideline_2023_1130_ErrorCorrection_2025.pdf
  12. U.S. Food and Drug Administration. “Bioanalytical Method Validation Guidance for Industry.” FDA Guidance Document. 2018. fda.gov/regulatory-information/search-fda-guidance-documents/bioanalytical-method-validation-guidance-industry
  13. Mant CT, Chen Y, Yan Z, Popa TV, Kovacs JM, Mills JB, Tripet BP, Hodges RS. “HPLC Analysis and Purification of Peptides.” Methods in Molecular Biology. 2007. pmc.ncbi.nlm.nih.gov/articles/PMC7119934/
  14. Zeng K, Geerlof-Vidavsky I, Gucinski A, Jiang X, Boyne MT. “Liquid Chromatography-High Resolution Mass Spectrometry for Peptide Drug Quality Control.” AAPS Journal. 2015. pmc.ncbi.nlm.nih.gov/articles/PMC4406950/
  15. D’Hondt M, Bracke N, Taevernier L, Gevaert B, Verbeke F, Wynendaele E, De Spiegeleer B. “Related impurities in peptide medicines.” Journal of Pharmaceutical and Biomedical Analysis. 2014. sciencedirect.com/science/article/abs/pii/S0731708514003008
  16. Stoll DR, et al. “A Strategy for assessing peak purity of pharmaceutical peptides in reversed-phase chromatography methods using two-dimensional liquid chromatography.” Journal of Chromatography A. 2023. pubmed.ncbi.nlm.nih.gov/36871316/
  17. International Council for Harmonisation. “Q1A(R2) Stability Testing of New Drug Substances and Products.” ICH Harmonised Guideline. 2003. database.ich.org/sites/default/files/Q1A%28R2%29%20Guideline.pdf
  18. World Health Organization. “Model guidance for the storage and transport of time- and temperature-sensitive pharmaceutical products.” WHO Technical Report Series, Annex 9. 2011. who.int/docs/default-source/medicines/norms-and-standards/guidelines/distribution/trs961-annex9-modelguidanceforstoragetransport.pdf
  19. Wang Y, Tomlinson B. “Tesamorelin, a human growth hormone releasing factor analogue.” Expert Opinion on Investigational Drugs. 2009. pubmed.ncbi.nlm.nih.gov/19243281/
  20. Spooner LM, Olin JL. “Tesamorelin: a growth hormone-releasing factor analogue for HIV-associated lipodystrophy.” Annals of Pharmacotherapy. 2012. pubmed.ncbi.nlm.nih.gov/22298602/
  21. Bedimo R, et al. “Growth hormone and tesamorelin in the management of HIV-associated lipodystrophy.” HIV/AIDS – Research and Palliative Care. 2011. pubmed.ncbi.nlm.nih.gov/22096409/
  22. Falutz J, et al. “Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog in human immunodeficiency virus-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind placebo-controlled phase 3 trials.” Journal of Clinical Endocrinology and Metabolism. 2010. pubmed.ncbi.nlm.nih.gov/20554713/
  23. Stanley TL, et al. “Effects of a growth hormone-releasing hormone analog on endogenous GH pulsatility and insulin sensitivity in healthy men.” Journal of Clinical Endocrinology and Metabolism. 2011. pubmed.ncbi.nlm.nih.gov/20943777/
  24. Knoop A, Thomas A, Fichant E, Thevis M. “Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS.” Analytical and Bioanalytical Chemistry. 2016. pubmed.ncbi.nlm.nih.gov/26879649/
  25. Thomas A, Walpurgis K, Thevis M. “Chromatographic-mass spectrometric analysis of peptidic analytes (2-10 kDa) in doping control urine samples.” Journal of Mass Spectrometry. 2024. pubmed.ncbi.nlm.nih.gov/38197510/
  26. Uçaktürk E, Nemutlu E. “Analysis of growth hormone releasing hormone and its analogs in urine using nano liquid chromatography coupled with quadrupole/orbitrap mass spectrometry.” Journal of Pharmaceutical and Biomedical Analysis. 2026. pubmed.ncbi.nlm.nih.gov/41138283/

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