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Semaglutide

Identification

Property Value
CAS Number 910463-68-2
Molecular Formula C₁₈₇H₂₉₁N₄₅O₅₉
Molecular Weight ~4,113.6 Da
Sequence Length 31 amino acids (engineered GLP-1 analog)
Appearance White to off-white lyophilized powder
Solubility Soluble in aqueous buffers at physiological pH

Structural Features

Semaglutide is a structurally modified GLP-1 (7-37) analog engineered for extended pharmacokinetic half-life and resistance to enzymatic degradation:

Modification Purpose
Aib⁸ (α-aminoisobutyric acid) Substitution at position 8 confers resistance to dipeptidyl peptidase-4 (DPP-4) cleavage
C18 fatty diacid linker Conjugated to Lys²⁶ via a gamma-glutamyl-2xOEG spacer; enables high-affinity, reversible albumin binding
Arg³⁴ substitution Replaces native Lys³⁴, preventing mis-acylation and improving manufacturing selectivity

Half-Life Rationale

The C18 fatty diacid-albumin binding mechanism extends the circulating half-life to approximately 7 days in preclinical models, enabling once-weekly administration protocols. Albumin binding reduces renal clearance and protects the peptide from rapid proteolysis.

Comparator Analysis

Parameter Semaglutide Tirzepatide Retatrutide
Receptor Target GLP-1R (selective) GIPR / GLP-1R (dual) GIPR / GLP-1R / GCGR (triple)
Molecular Weight ~4,113.6 Da ~4,813.5 Da ~4,845.5 Da
Amino Acid Count 31 39 39
Half-Life ~7 days ~5 days ~6 days
Synthesis Complexity High Very High Complex
DPP-4 Resistance Yes (Aib⁸) Yes Yes
Albumin Binding C18 fatty diacid C20 fatty diacid C20 fatty diacid

Research Applications

Semaglutide is investigated across a broad range of metabolic research domains:

Research Area Key Findings in Preclinical & Clinical Literature
Glucose Homeostasis Glucose-dependent insulin secretion enhancement; glucagon suppression during euglycemia and hyperglycemia
Body Weight Regulation Central and peripheral appetite suppression; delayed gastric emptying; reduced energy intake
Cardiovascular Outcomes MACE risk reduction in type 2 diabetes populations; systolic blood pressure improvement
NASH / MASLD Reduction in hepatic steatosis, lobular inflammation, and ballooning in biopsy-confirmed NASH
Renal Protection Reduction in albuminuria; attenuation of eGFR decline in chronic kidney disease
Neuroprotection Investigation in Parkinson's and Alzheimer's disease models via GLP-1R-mediated anti-inflammatory pathways

Quality Specifications

Parameter Specification Method
Purity (HPLC) ≥99.0% Reverse-phase HPLC, 214 nm
Mass Identity MW ±1.0 Da ESI-MS or MALDI-TOF
Water Content ≤5.0% Karl Fischer titration
Peptide Content ≥80.0% Amino acid analysis
Linker Integrity Intact C18 fatty diacid conjugate (bulk orders) LC-MS characterization of intact conjugate
Trifluoroacetate ≤0.1% (acetate salt form) Ion chromatography
Endotoxin ≤1.0 EU/mg LAL kinetic chromogenic
Residual Solvents ≤ ICH Q3C limits Headspace GC
pH 5.0–7.5 (1 mg/mL) Potentiometric

Linker Integrity Note: For bulk orders (>100 vials), a dedicated linker integrity verification by LC-MS is included in the standard quality package. This confirms the intact C18 fatty diacid conjugate, critical for pharmacological activity.

Available Configurations

Format Size Vials per Kit
Standard Research Kit 5 mg × 10 vials 10
Extended Research Kit 10 mg × 10 vials 10
Custom Configuration Up to 25 mg/vial Per project scope

Storage & Stability

Condition Requirement
Short-term 2–8°C, lyophilized form, protect from light
Long-term −20°C to −80°C, desiccated
Reconstituted 24 h at 2–8°C; aliquot and freeze at −20°C for extended storage
Shipping Cold chain (2–8°C) recommended for international shipments; ambient acceptable for ≤7 days

Documentation

  • COA provided per batch with full chromatographic and mass spectrometric data
  • MSDS supplied with each shipment
  • Linker Integrity Report included for bulk orders (HPLC-MS confirmation of intact C18-fatty diacid conjugate)

Special Notes

  • FOR LABORATORY RESEARCH USE ONLY.
  • Aib⁸ incorporation increases synthetic complexity; batch-to-batch consistency is verified by HPLC-MS.
  • The C18 fatty diacid linker is hydrophobic; reconstitution may require gentle agitation and pH adjustment.

Key Research References

Reference PMID Key Finding
Lau J et al. "Discovery of the once-weekly glucagon-like peptide-1 (GLP-1) analogue semaglutide." J Med Chem. 2015;58(18):7370–7380. 26308095 Engineering of semaglutide with Aib⁸ substitution for DPP-4 resistance and C18 fatty diacid for albumin binding; 7-day half-life demonstrated
Marso SP et al. "Semaglutide and cardiovascular outcomes in patients with type 2 diabetes." N Engl J Med. 2016;375(19):1834–1844. 27633186 SUSTAIN-6 trial: semaglutide reduced MACE outcomes in T2D; established cardiovascular benefit for GLP-1 RA class
Newsome PN et al. "A placebo-controlled trial of subcutaneous semaglutide in nonalcoholic steatohepatitis." N Engl J Med. 2021;384(12):1113–1124. 33185364 Semaglutide significantly improved NASH resolution without worsening fibrosis in biopsy-confirmed NASH patients

Stability & Storage

Condition Degradation Profile
Lyophilized Storage Standard lyophilized peptide stability; no special handling beyond desiccated, temperature-controlled storage. 24 months at 2–8°C, 36 months at −20°C
Neutral pH (5.0–7.5) Stable; recommended pH for reconstitution and working solutions
Acidic pH (<4.0) May promote aggregation of the hydrophobic C18 linker; avoid strongly acidic buffers
Alkaline pH (>8.0) Risk of deamidation and C18 linker hydrolysis over extended periods
Temperature Stress The C18 fatty diacid linker is hydrophobic; can aggregate or precipitate under temperature fluctuations. Gentle agitation required during reconstitution
Reconstituted Solution 24 h at 2–8°C; aliquot and freeze at −20°C for ≤30 days. Avoid repeated freeze-thaw

Frequently Asked Questions

Q: What purity specifications apply to semaglutide?

≥99.0% by HPLC at 214 nm with ESI-MS mass identity confirmation (±1.0 Da). Additional QC includes peptide content (≥80.0%), water content (≤5.0%), and linker integrity verification by LC-MS for bulk orders. The Aib⁸ substitution and intact C18 fatty diacid conjugate are confirmed in every batch-specific COA.

Q: How should semaglutide be stored after reconstitution?

Reconstituted semaglutide is stable for 24 hours at 2–8°C. For longer storage, aliquot into single-use sterile vials and freeze at −20°C (stable ≤30 days). Do not store in alkaline buffers (pH > 8) which can cause deamidation and linker hydrolysis. The hydrophobic C18 linker may require gentle agitation during reconstitution — never vortex or shake vigorously. Avoid repeated freeze-thaw cycles.

Source & Purchase

For researchers requiring SEMAGLUTIDE with full analytical documentation including HPLC and LC-MS traces, visit the PeptideSourceHub product page for bulk pricing and specifications.

Purchase SEMAGLUTIDE with COA →

Product Link
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Retatrutide (Triple Agonist) retatrutide.md — Triple GIPR/GLP-1R/GCGR agonist
Cagrilintide (Amylin Analog) cagrilintide.md — Long-acting amylin receptor agonist
AOD-9604 (hGH Fragment) aod-9604.md — Lipolytic hGH fragment 177-191