Semaglutide Fragment 5-31 Impurity Reference Standard

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Sku: BF-SMG-Fragment-5-31
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In stock & estimated to ship in 3-7 days by October 14, 2026
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Description

Semaglutide Fragment 5-31 impurity is a high-purity impurity reference standard designed for pharmaceutical quality control, analytical method development, and regulatory compliance testing of Semaglutide. This impurity is a truncated sequence fragment of Semaglutide (Fragment 5-31), arising from incomplete synthesis or backbone cleavage. This reference material supports accurate impurity identification, structural confirmation, and quantitative analysis by HPLC and LC-MS in peptide drug development and manufacturing workflows.

Specifications

Parameter Value
API Category Semaglutide Impurity
Appearance Off-white lyophilized powder
Catalog Number BF-SMG-Fragment-5-31
Package Size 50 mg (custom sizes available upon request)
Purity ≥95% (HPLC)
Salt Form Sodium salt
CAS Number N/A
Parent Compound CAS 910463-68-2 (Semaglutide)
Molecular Formula N/A
Molecular Weight N/A
Solubility 20% ACN in water
Storage Condition -20±5°C, protect from light and moisture
Synonyms [Fragment 5-31]Semaglutide; Fragment impurity

Applications

  • Pharmaceutical impurity profiling and quality control

  • HPLC and LC-MS/MS method development and validation

  • Drug substance and drug product release testing

  • Stability studies and forced degradation analysis

  • Regulatory submission support (FDA, EMA, ICH guidelines)

Custom sizes and specifications are available upon request. Please use the Request a Quote button for pricing.

For research use only. Not intended for diagnostic or therapeutic use.

Documents

MSDS

COA

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