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Semaglutide
Peptology Ltd. · Peptides for weight loss
Semaglutide – a GLP-1 receptor agonist, research peptide. Purity 99%+, HPLC/MS report for every batch.
📦 The product is in our EU warehouse – delivery within 3–5 working days.
50,00 € · In stock
For research use only / Not a medicine









| Purity | >99% |
|---|---|
| Method | HPLC + LC/MS |
| Laboratory | Analiza Białek |
| Batch | 0226 |
Last updated: 19/10/2026
Semaglutide (also known as semaglutide) is a synthetic, long-acting GLP-1 receptor agonist (glucagon-like peptide-1). It is an acylated analog of human GLP-1 in which an attached fatty-acid residue provides strong binding to albumin — which gives the molecule a long half-life and enables once-weekly dosing. In the clinical literature, Semaglutide is described as one of the best-studied agonists of the GLP-1 class, with data on glucose-dependent insulin secretion and metabolic markers.
Semaglutide is a mono-agonist — it acts only on the GLP-1 axis. This distinguishes it from the dual agonist Tirzepatide (GLP-1/GIP) and the triple agonist Retatrutide (GLP-1/GIP/glucagon). In publications, Semaglutide is often used as the reference GLP-1 agonist against which newer multi-receptor molecules are compared.
The research-grade Semaglutide offered by Peptology is not a registered medicine — it is a lyophilized research peptide intended exclusively for scientific and in vitro applications, not intended for use in humans or animals. See also the other peptides for weight loss (GLP-1) in our category.
In the version offered by Peptology, Semaglutide is supplied as a lyophilized peptide with purity above 99% (HPLC/MS), confirmed by independent laboratory analysis (CoA for every batch). It is available in two vial formats — 5 mg and 10 mg — depending on the scale of the research protocol.
Semaglutide is available in two lyophilized formats, which cover different research-work scales — from single in vitro series to longer protocols with higher peptide consumption.
5 MG
Standard format
Suitable for validation experiments, single in vitro series and short-term laboratory protocols.
10 MG
Enlarged format
For longer research series, repeated cell models and protocols with higher peptide consumption.
Both formats have identical purity > 99% and the same laboratory certificate for the batch. The choice of size depends on the scale of the protocol, not on the concentration of the active substance.
GLP-1 receptors are found in the pancreas, brain and gastrointestinal tract. In clinical and preclinical publications, Semaglutide is described as a molecule that activates these receptors and produces several complementary metabolic effects. The main parameters studied are glucose-dependent insulin secretion, glucagon secretion and gastric emptying.
GLP-1 RECEPTOR
Activation of the GLP-1 receptor, including in central pathways, is described in the literature through intracellular cAMP signaling.
GLUCOSE & INSULIN
Semaglutide stimulates glucose-dependent insulin secretion and suppresses glucagon secretion — linked in studies to improved HbA1c and glucose homeostasis.
GASTRIC EMPTYING
Slowed gastric emptying is described in the literature as an effect of GLP-1 receptor activation in the gastrointestinal tract.
GLP-1 is an incretin secreted after a meal that simultaneously regulates insulin secretion, glucagon secretion and gastric emptying. Semaglutide's long half-life — a result of albumin binding — maintains continuous activation of this axis throughout the week, which distinguishes it from short-acting GLP-1 analogs. In studies, this profile is linked to improved glycemic markers.
Semaglutide is a point of reference for newer multi-receptor molecules. The dual agonist Tirzepatide adds the GIP axis, and the triple agonist Retatrutide — additionally the glucagon axis. The results presented come from controlled clinical trials and do not constitute a claim about the effect of the research-grade product.
Semaglutide is an acylated GLP-1 analog which, in published pharmacokinetic data, is described as a molecule with a long half-life thanks to strong binding to albumin — which explains the weekly dosing schedule used in clinical protocols.
The table below compares Semaglutide with two newer multi-receptor molecules from the incretin family in the research-peptide catalog. All three are studied with respect to glucose metabolism, but they differ in the number of activated receptor axes — Semaglutide acts on one (GLP-1), Tirzepatide on two (GLP-1/GIP), and Retatrutide on three (GLP-1/GIP/glucagon). The data are of a scientific-comparative nature and do not constitute a direct head-to-head comparison.
| Semaglutide | Tirzepatide | Retatrutide | |
|---|---|---|---|
| Mechanism | GLP-1 mono-agonist | Dual GLP-1 / GIP agonist | Triple GLP-1 / GIP / glucagon agonist |
| Receptor axes | 1 | 2 | 3 |
| CAS number | 910463-68-2 | 2023788-19-2 | 2381089-83-2 |
| Half-life | ~7 days | ~5 days | ~6 days |
| Weight reduction in trials | ~14.9% (68 weeks, STEP 1) | up to ~22.5% | up to ~24% (phase 2) |
| In the Peptology catalog | Lyophilized powder · 5/10 mg · research use only | Lyophilized powder · 5/10/15/30 mg · research use only | Lyophilized powder · 5/10/15/30 mg · research use only |
Sources: Wilding et al., STEP 1, New England Journal of Medicine (2021); the SUSTAIN program (type 2 diabetes); the SELECT study (cardiovascular outcomes, NEJM 2023, n=17,604). The data presented come from different clinical programs and should not be interpreted as a direct comparison or as a claim about the effect of a specific research-grade product.
Semaglutide is among the best-studied GLP-1 agonists. The clinical program covers three large lines — type 2 diabetes (SUSTAIN), obesity (STEP) and cardiovascular outcomes (SELECT). These results concern the pharmaceutical forms of semaglutide and come from controlled clinical trials.
Early clinical studies documented good tolerability, a long half-life (~7 days) resulting from binding to albumin, and the achievement of steady state after 4–5 weeks of weekly dosing.
The SUSTAIN program evaluated semaglutide in patients with type 2 diabetes, demonstrating a significant reduction in HbA1c and body weight compared with placebo and other antidiabetic medicines.
In the phase 3 STEP 1 study, adults with obesity or overweight received semaglutide 2.4 mg SC weekly or placebo for 68 weeks, together with a lifestyle change. The mean body-weight reduction was −14.9% in the semaglutide group versus −2.4% in the placebo group, and a body-weight reduction of ≥ 5% was achieved by 86.4% of participants (versus 31.5% in the placebo group). These results come from a controlled clinical trial and do not constitute a recommendation for individual use.
In the SELECT study (17,604 participants with cardiovascular disease and overweight/obesity, without diabetes), semaglutide 2.4 mg was linked to a 20% reduction in the risk of major adverse cardiovascular events (MACE) — cardiovascular death, heart attack or stroke — compared with placebo. These are data from a controlled clinical trial.
Note: The clinical trial information concerns the pharmaceutical forms of semaglutide and is presented for scientific and informational purposes. It does not constitute medical advice, a recommendation for use or a claim about the effect of the research-grade product offered by Peptology.
All results given concern published clinical trials of the pharmaceutical forms of semaglutide and should not be interpreted as a promise of effect, an instruction for use or a claim about the effect of the research-grade product offered by Peptology.
Important: The information below describes doses used in published clinical trials of the pharmaceutical forms of semaglutide. It is provided for scientific and informational purposes and does not constitute a recommendation for individual use, medical advice or administration instructions. The research-grade Semaglutide offered by Peptology is not a registered medicine.
In clinical programs, semaglutide was used in a weekly subcutaneous schedule with gradual dose titration — which aims to improve gastrointestinal tolerability:
Like Tirzepatide and Retatrutide, Semaglutide in studies requires slow titration to improve tolerability — patients were started on a lower dose and it was gradually increased. These schedules are part of controlled clinical trials and do not constitute a recommendation for self-administration.
Semaglutide is supplied as a lyophilized (freeze-dried) powder in a vial. In lyophilized form the peptide is stable at room temperature, protected from light and moisture — refrigeration before reconstitution is not mandatory. After reconstitution, stability depends on the solvent used, with Peptide Matrix Water™ significantly extending the peptide's lifespan.
Laboratory tip: With your order, you can add Peptide Matrix Water™ to the cart — a stabilizing solution designed for working with reconstituted research peptides, including GLP-1 agonists. More in the article Bacteriostatic water vs acetic acid vs matrix water.
Semaglutide is a synthetic, long-acting GLP-1 receptor agonist. It mimics the action of the incretin GLP-1, which regulates insulin secretion, glucagon secretion and gastric emptying. In clinical trials it is one of the most frequently evaluated peptides in the context of obesity and type 2 diabetes. The results come from controlled clinical trials.
All three are studied with respect to glucose metabolism, but they differ in the number of receptor axes. Semaglutide acts only on the GLP-1 axis, Tirzepatide combines GLP-1 and GIP, and Retatrutide adds a third axis — the glucagon receptor. In studies, Semaglutide often serves as the reference against which the newer multi-receptor molecules are compared.
The biological half-life of semaglutide is about 7 days thanks to strong binding to albumin, and steady state is reached after 4–5 weeks. This is why clinical protocols use a weekly schedule — similar to Tirzepatide or Retatrutide.
Both formats have identical purity > 99% and the same batch certificate. The choice depends on the scale of the protocol: 5 mg for single validation series and shorter protocols, and 10 mg for longer, repeated models with higher peptide consumption.
The lyophilized vial is stored at room temperature, protected from light and moisture — without the need for cooling before reconstitution. After reconstitution, stability depends on the solvent: with Peptide Matrix Water™ — up to 60 days in the refrigerator +2 °C to +8 °C; with bacteriostatic or sterile water — up to 28 days. In all cases avoid refreezing.
Peptology offers Semaglutide as a research peptide with confirmed purity above 99% (HPLC/MS) and independent laboratory analysis for every batch. Fast shipping, discreet packaging and certificates of purity with the product. For scientific background, also see the article Peptides — what they are, how they work, main categories and safety profile.
Researchers working with Semaglutide often also consider other molecules from the GLP-1 / incretin agonist class and solutions for reconstitution. Each of the products below has a certificate of purity above 99%:
Tirzepatide
Dual GLP-1 / GIP agonist
Retatrutide
Triple GLP-1 / GIP / glucagon agonist
Cagrilintide
Long-acting amylin analog
CS10 (Cagrilintide + Semaglutide)
Ready-made research combination
Bacteriostatic water
Standard solvent for peptides
Peptide Matrix Water™
Stabilizing solution for reconstitution
See the full catalog: Peptides for weight loss (GLP-1) · Solutions for peptides · Blog on peptide research
Research warning: Semaglutide is offered exclusively for scientific research and in vitro purposes. It is not a medicinal product, is not an approved medicine, is not intended for use in humans or animals, and does not replace medical advice. All clinical trial information concerns the pharmaceutical forms of semaglutide and is provided for scientific and informational purposes; it does not constitute a claim about the effect of the research-grade product offered by Peptology.
| CAS number | 910463-68-2 |
|---|---|
| Molecular weight | 4114 g/mol |
| Molecular formula | C187H291N45O59 |
| Class | GLP-1 receptor agonist |
| Form | Lyophilised powder in a glass vial |
| Storage | Lyophilisate: 2–8 °C, dry and protected from light · after reconstitution: 2–8 °C |
Standardized protocol applicable to all research peptides in the Peptology catalogue. To calculate the solution concentration (mg/mL) for each vial, use the peptide reconstitution calculator.
1. SOLVENT
2. RECONSTITUTION
Add the solvent down the side of the vial, without shaking, wait 10–15 min.
3. CALCULATION
Calculator → concentration mg/mL
4. STORAGE
+2 °C to +8 °C, up to 60 days with Peptide Matrix Water
| Parameter | Value |
|---|---|
| Form | Lyophilized powder |
| Solvent | Peptide Matrix Water |
| Reconstitution volume | 1–3 mL — maximum 3 mL (capacity of the standard vial) |
| Storage before reconstitution | Room temperature, protected from direct light (refrigeration not required) |
| After reconstitution | Up to 60 days at +2 °C to +8 °C with Peptide Matrix Water |
Precision pipette
Calibrated, 100–1000 µL — for accurately measuring the volume of solvent added to the vial.
70% alcohol swabs
Two swabs — to disinfect the peptide vial and the solvent vial.
Stabilized solvent for lyophilized peptides. Why this one.
| ✅ Correct | ❌ Mistake |
|---|---|
| Disinfect the vial caps and the work surface with 70% alcohol; wear gloves | Working without disinfection |
| Add the solvent slowly along the vial wall | Direct jet onto the powder — foaming and denaturation |
| Gentle rolling between the palms | Shaking — foam, which denatures peptides |
| 10–15 minutes waiting at room temperature | Mechanical mixing or heating |
| Visual check: clear, particle-free | Working with a cloudy or discolored solution |
⚠️ Maximum 3 mL solvent. The standard vial does not accommodate larger volumes — do not exceed during reconstitution.
Reconstitution per vial — solvent: Peptide Matrix Water. Concentration after adding the solvent (1 mg/mL = 1 µg/µL):
| Vial | + 1 mL | + 2 mL | + 3 mL |
|---|---|---|---|
| 5 mg | 5 mg/mL | 2.5 mg/mL | 1.67 mg/mL |
| 10 mg | 10 mg/mL | 5 mg/mL | 3.33 mg/mL |
👉 For any vial and solvent volume — use the calculator. It calculates the concentration (mg/mL, µg/µL) and the volume per sample (mL, µL).
BEFORE RECONSTITUTION
Room temperature, protected from direct light, in original packaging. Refrigerator not required.
AFTER RECONSTITUTION
+2 °C to +8 °C, up to 60 days with Peptide Matrix Water. Discard any remainder after this period.
FREEZING
Not recommended. Freeze/thaw cycles degrade peptide structure.
1. Shaking "to dissolve faster"
Foam = denaturation. Only gentle rolling between the palms.
2. Inappropriate solvent
For peptide stability use only sterile, specially formulated solvent — recommended Peptide Matrix Water.
3. Ignoring slight turbidity
Not fully clear = the sample does not meet the criteria for use.
4. Taking it out of the refrigerator "for an hour–two"
Short exposures add up and compromise stability.
Research status: All Peptology products are intended for laboratory and research use only. They are not medicinal products, not approved for human or veterinary use and do not substitute medical advice. The described protocol is standard laboratory practice for working with lyophilized peptides.
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It is supplied as a lyophilized (freeze-dried) powder in a sealed vial. Store the unopened vial dry and protected from light, ideally at 2–8 °C. After laboratory reconstitution, keep the solution at 2–8 °C and use it within the period stated in the “Laboratory reconstitution” tab (up to 60 days with Peptide Matrix Water).
Every batch has a purity of 99% or higher, confirmed by HPLC and mass spectrometry (MS) and documented in a certificate of analysis (CoA). The report for the current batch is shown in the “Laboratory Analysis” tab.
No. Offered for research purposes, without the need for a prescription.
You can buy Semaglutide in Europe online from Peptology, from 50,00 €. Delivery with GLS in 3–5 working days. Shipping is free from 50,00 €. Payment by card or bank transfer. Purity 99%+, with an HPLC report for every batch.



