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Sigma-Aldrich™ Fmoc-Trp(Boc)-OH ≥97.0% (HPLC), for peptide synthesis

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SKU: 47561-5G-F
Brand: Sigma-Aldrich
UoM: Each
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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 Each
Estimated delivery Estimated delivery: 4-8 weeks
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Fmoc-Trp(Boc)-OH is a high-purity, selectively protected tryptophan derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group and Boc protection on the indole nitrogen of tryptophan, enabling controlled peptide elongation while helping to reduce unwanted side reactions involving the indole side chain.

This reagent is widely used in custom peptide synthesis, pharmaceutical research, proteomics, drug discovery, enzyme-substrate studies, structural biology, protein engineering, and bioorganic chemistry. Tryptophan-containing peptides are particularly valuable in studies involving protein folding, hydrophobic interactions, fluorescence, and peptide–receptor interactions.

Key Features

FeatureDetails
High Purity≥97.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Boc Side-Chain ProtectionProtects the tryptophan indole nitrogen during peptide synthesis
Reduced Side ReactionsHelps minimize unwanted oxidation or modification of the indole ring
SPPS CompatibleSuitable for incorporation of tryptophan into synthetic peptides
Research ApplicationsIdeal for peptide chemistry, drug discovery, protein engineering, and structural biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Trp(Boc)-OH, ≥97.0% HPLC
CAS Number143824-78-6
Empirical FormulaC₃₁H₃₀N₂O₆
Molecular Weight526.58 g/mol
Beilstein Registry Number7698009
MDL NumberMFCD00153366
PubChem Substance ID57651011
Optical Activity[α]²⁰/D -21 ± 2°; c = 1% in DMF
FormSolid
Assay≥97.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, Boc, carboxylic acid

Applications

Fmoc-Trp(Boc)-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of tryptophan residues into synthetic peptides
  • Custom peptide synthesis and peptide modification
  • Peptide-based pharmaceutical and drug discovery research
  • Enzyme-substrate and inhibitor studies
  • Protein engineering and structural biology research
  • Fluorescence-related peptide and protein studies
  • Bioorganic chemistry and peptidomimetic synthesis
  • Synthesis of tryptophan-containing therapeutic peptide analogs

Ordering Information

Catalog NumberQuantity
47561-5G-F5 g
47561-25G-F25 g
47561-100G-F100 g
47561-1KG-F1 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, and extreme temperatures. 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-Trp(Boc)-OH is a high-purity, selectively protected tryptophan derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group and Boc protection on the indole nitrogen of tryptophan, enabling controlled peptide elongation while helping to reduce unwanted side reactions involving the indole side chain.

This reagent is widely used in custom peptide synthesis, pharmaceutical research, proteomics, drug discovery, enzyme-substrate studies, structural biology, protein engineering, and bioorganic chemistry. Tryptophan-containing peptides are particularly valuable in studies involving protein folding, hydrophobic interactions, fluorescence, and peptide–receptor interactions.

Key Features

FeatureDetails
High Purity≥97.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Boc Side-Chain ProtectionProtects the tryptophan indole nitrogen during peptide synthesis
Reduced Side ReactionsHelps minimize unwanted oxidation or modification of the indole ring
SPPS CompatibleSuitable for incorporation of tryptophan into synthetic peptides
Research ApplicationsIdeal for peptide chemistry, drug discovery, protein engineering, and structural biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Trp(Boc)-OH, ≥97.0% HPLC
CAS Number143824-78-6
Empirical FormulaC₃₁H₃₀N₂O₆
Molecular Weight526.58 g/mol
Beilstein Registry Number7698009
MDL NumberMFCD00153366
PubChem Substance ID57651011
Optical Activity[α]²⁰/D -21 ± 2°; c = 1% in DMF
FormSolid
Assay≥97.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, Boc, carboxylic acid

Applications

Fmoc-Trp(Boc)-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of tryptophan residues into synthetic peptides
  • Custom peptide synthesis and peptide modification
  • Peptide-based pharmaceutical and drug discovery research
  • Enzyme-substrate and inhibitor studies
  • Protein engineering and structural biology research
  • Fluorescence-related peptide and protein studies
  • Bioorganic chemistry and peptidomimetic synthesis
  • Synthesis of tryptophan-containing therapeutic peptide analogs

Ordering Information

Catalog NumberQuantity
47561-5G-F5 g
47561-25G-F25 g
47561-100G-F100 g
47561-1KG-F1 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, and extreme temperatures. 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-Trp(Boc)-OH is a high-purity, selectively protected tryptophan derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group and Boc protection on the indole nitrogen of tryptophan, enabling controlled peptide elongation while helping to reduce unwanted side reactions involving the indole side chain.

This reagent is widely used in custom peptide synthesis, pharmaceutical research, proteomics, drug discovery, enzyme-substrate studies, structural biology, protein engineering, and bioorganic chemistry. Tryptophan-containing peptides are particularly valuable in studies involving protein folding, hydrophobic interactions, fluorescence, and peptide–receptor interactions.

Key Features

FeatureDetails
High Purity≥97.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Boc Side-Chain ProtectionProtects the tryptophan indole nitrogen during peptide synthesis
Reduced Side ReactionsHelps minimize unwanted oxidation or modification of the indole ring
SPPS CompatibleSuitable for incorporation of tryptophan into synthetic peptides
Research ApplicationsIdeal for peptide chemistry, drug discovery, protein engineering, and structural biology

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Trp(Boc)-OH, ≥97.0% HPLC
CAS Number143824-78-6
Empirical FormulaC₃₁H₃₀N₂O₆
Molecular Weight526.58 g/mol
Beilstein Registry Number7698009
MDL NumberMFCD00153366
PubChem Substance ID57651011
Optical Activity[α]²⁰/D -21 ± 2°; c = 1% in DMF
FormSolid
Assay≥97.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, Boc, carboxylic acid

Applications

Fmoc-Trp(Boc)-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of tryptophan residues into synthetic peptides
  • Custom peptide synthesis and peptide modification
  • Peptide-based pharmaceutical and drug discovery research
  • Enzyme-substrate and inhibitor studies
  • Protein engineering and structural biology research
  • Fluorescence-related peptide and protein studies
  • Bioorganic chemistry and peptidomimetic synthesis
  • Synthesis of tryptophan-containing therapeutic peptide analogs

Ordering Information

Catalog NumberQuantity
47561-5G-F5 g
47561-25G-F25 g
47561-100G-F100 g
47561-1KG-F1 kg

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, oxidation, and extreme temperatures. 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, 5g, 25g