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Sigma-Aldrich™ Novabiochem® Fmoc-OSu ≥99.0% (HPLC), for peptide synthesis

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SKU: 8510141000
Brand: Sigma-Aldrich
UoM: sngls
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LabMart Limited - Tamale
NS-246, Via, 4388 Tamale-Kumbungu Rd, Tamale, Northern Region, Ghana
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LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
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MOQ : 1.0 sngls
Estimated delivery Estimated delivery: 4-8 weeks
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Fmoc-OSu, also known as N-(9-Fluorenylmethoxycarbonyloxy)succinimide, is a high-purity Fmoc transfer reagent used for amine protection, amino acid derivatization, peptide synthesis, and biomolecule functionalization. It is commonly used to introduce the Fmoc protecting group onto amino acids, peptides, and other amine-containing molecules.

As a reactive succinimidyl ester, Fmoc-OSu enables efficient and selective N-terminal or amine functionalization under suitable reaction conditions. It is widely used in Fmoc-based solid-phase peptide synthesis (SPPS), medicinal chemistry, bioorganic chemistry, chemical biology, biomaterial functionalization, and peptide reagent preparation.

Key Features

FeatureDetails
High Purity≥99.0% by HPLC for reliable synthetic performance
Fmoc Transfer ReagentIntroduces Fmoc protection onto amino acids, peptides, and amines
Reactive Succinimidyl EsterEnables efficient and selective amine functionalization
SPPS CompatibleUseful in workflows supporting Fmoc-based peptide synthesis
Low Impurity ProfileHelps reduce unwanted byproducts in Fmoc derivatization
Versatile Research UseSuitable for peptide chemistry, medicinal chemistry, biomaterials, and chemical biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-OSu, ≥99.0% HPLC
Full NameN-(9-Fluorenylmethoxycarbonyloxy)succinimide
CAS Number82911-69-1
Empirical FormulaC₁₉H₁₅NO₅
Molecular Weight337.33 g/mol
MDL NumberMFCD00010733
EC Index Number433-520-5
UNSPSC Code12352108
FormPowder
Melting Point145–148 °C
Assay≥99.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, succinimidyl ester

Applications

Fmoc-OSu is suitable for:

  • Preparation of Fmoc-protected amino acids
  • Selective amine protection and functionalization
  • Fmoc-based peptide synthesis workflows
  • Amino acid derivatization
  • Peptide and small-molecule modification
  • Medicinal chemistry and drug discovery research
  • Biomolecule and biomaterial functionalization
  • Surface chemistry and synthetic biointerface design
  • Chemical biology and bioengineering applications
  • Sequence-defined peptide and polymer functionalization

Ordering Information

Catalog NumberQuantity
851014002525 g
8510140100100 g
85101410001 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, strong acids, strong bases, and nucleophiles. Handle in a suitable laboratory environment using appropriate personal protective equipment, including gloves, lab coat, and safety goggles.

Research Use Statement

For Research Use Only (RUO). Not intended for diagnostic or therapeutic use.

Application: Protein Biology, Peptide Synthesis
Storage Temperature: 2-8°C
Product Type: Amino Acid & Biochemicals
Product Brand: Sigma-Aldrich
Product Grade: HPLC Grade

Fmoc-OSu, also known as N-(9-Fluorenylmethoxycarbonyloxy)succinimide, is a high-purity Fmoc transfer reagent used for amine protection, amino acid derivatization, peptide synthesis, and biomolecule functionalization. It is commonly used to introduce the Fmoc protecting group onto amino acids, peptides, and other amine-containing molecules.

As a reactive succinimidyl ester, Fmoc-OSu enables efficient and selective N-terminal or amine functionalization under suitable reaction conditions. It is widely used in Fmoc-based solid-phase peptide synthesis (SPPS), medicinal chemistry, bioorganic chemistry, chemical biology, biomaterial functionalization, and peptide reagent preparation.

Key Features

FeatureDetails
High Purity≥99.0% by HPLC for reliable synthetic performance
Fmoc Transfer ReagentIntroduces Fmoc protection onto amino acids, peptides, and amines
Reactive Succinimidyl EsterEnables efficient and selective amine functionalization
SPPS CompatibleUseful in workflows supporting Fmoc-based peptide synthesis
Low Impurity ProfileHelps reduce unwanted byproducts in Fmoc derivatization
Versatile Research UseSuitable for peptide chemistry, medicinal chemistry, biomaterials, and chemical biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-OSu, ≥99.0% HPLC
Full NameN-(9-Fluorenylmethoxycarbonyloxy)succinimide
CAS Number82911-69-1
Empirical FormulaC₁₉H₁₅NO₅
Molecular Weight337.33 g/mol
MDL NumberMFCD00010733
EC Index Number433-520-5
UNSPSC Code12352108
FormPowder
Melting Point145–148 °C
Assay≥99.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, succinimidyl ester

Applications

Fmoc-OSu is suitable for:

  • Preparation of Fmoc-protected amino acids
  • Selective amine protection and functionalization
  • Fmoc-based peptide synthesis workflows
  • Amino acid derivatization
  • Peptide and small-molecule modification
  • Medicinal chemistry and drug discovery research
  • Biomolecule and biomaterial functionalization
  • Surface chemistry and synthetic biointerface design
  • Chemical biology and bioengineering applications
  • Sequence-defined peptide and polymer functionalization

Ordering Information

Catalog NumberQuantity
851014002525 g
8510140100100 g
85101410001 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, strong acids, strong bases, and nucleophiles. Handle in a suitable laboratory environment using appropriate personal protective equipment, including gloves, lab coat, and safety goggles.

Research Use Statement

For Research Use Only (RUO). Not intended for diagnostic or therapeutic use.

No resources are currently available for this product.

This will display Shipping & Return.

Fmoc-OSu, also known as N-(9-Fluorenylmethoxycarbonyloxy)succinimide, is a high-purity Fmoc transfer reagent used for amine protection, amino acid derivatization, peptide synthesis, and biomolecule functionalization. It is commonly used to introduce the Fmoc protecting group onto amino acids, peptides, and other amine-containing molecules.

As a reactive succinimidyl ester, Fmoc-OSu enables efficient and selective N-terminal or amine functionalization under suitable reaction conditions. It is widely used in Fmoc-based solid-phase peptide synthesis (SPPS), medicinal chemistry, bioorganic chemistry, chemical biology, biomaterial functionalization, and peptide reagent preparation.

Key Features

FeatureDetails
High Purity≥99.0% by HPLC for reliable synthetic performance
Fmoc Transfer ReagentIntroduces Fmoc protection onto amino acids, peptides, and amines
Reactive Succinimidyl EsterEnables efficient and selective amine functionalization
SPPS CompatibleUseful in workflows supporting Fmoc-based peptide synthesis
Low Impurity ProfileHelps reduce unwanted byproducts in Fmoc derivatization
Versatile Research UseSuitable for peptide chemistry, medicinal chemistry, biomaterials, and chemical biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-OSu, ≥99.0% HPLC
Full NameN-(9-Fluorenylmethoxycarbonyloxy)succinimide
CAS Number82911-69-1
Empirical FormulaC₁₉H₁₅NO₅
Molecular Weight337.33 g/mol
MDL NumberMFCD00010733
EC Index Number433-520-5
UNSPSC Code12352108
FormPowder
Melting Point145–148 °C
Assay≥99.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, succinimidyl ester

Applications

Fmoc-OSu is suitable for:

  • Preparation of Fmoc-protected amino acids
  • Selective amine protection and functionalization
  • Fmoc-based peptide synthesis workflows
  • Amino acid derivatization
  • Peptide and small-molecule modification
  • Medicinal chemistry and drug discovery research
  • Biomolecule and biomaterial functionalization
  • Surface chemistry and synthetic biointerface design
  • Chemical biology and bioengineering applications
  • Sequence-defined peptide and polymer functionalization

Ordering Information

Catalog NumberQuantity
851014002525 g
8510140100100 g
85101410001 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, strong acids, strong bases, and nucleophiles. Handle in a suitable laboratory environment using appropriate personal protective equipment, including gloves, lab coat, and safety goggles.

Research Use Statement

For Research Use Only (RUO). Not intended for diagnostic or therapeutic use.

No resources are currently available for this product.

This will display Shipping & Return.

Specifications

Pack Size 1kg, 100g, 25g