Sigma-Aldrich™ Fmoc-Glu(OtBu)-OH, ≥98.0% (HPLC), for peptide synthesis

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Expédition : 2-3 jours ouvrables

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Specifications:
Application Protein Biology, Peptide Synthesis
Storage Temperature 2-8°C
Product Type Biochemical Reagent Forms Powder
Product Brand Sigma-Aldrich
Product Grade HPLC Grade Formula C₁₈H₁₇NO₅

Fmoc-Glu(OtBu)-OH (Fmoc-L-glutamic acid 5-tert-butyl ester) is a high-purity, protected amino acid derivative widely used in solid-phase peptide synthesis (SPPS) and bioconjugation chemistry. This reagent features:

  • Fmoc (9-fluorenylmethyloxycarbonyl) protection at the N-terminal for selective deprotection during peptide elongation.
  • tBu (tert-butyl) protection on the γ-carboxyl group, preventing unwanted side reactions and ensuring controlled peptide synthesis.

This reagent is a key building block in peptide synthesis, drug discovery, and biopolymer engineering, providing structural flexibility and chemical stability for peptide modifications.

Key Features & Benefits

High Purity (≥98.0%) – Ensures reliable and reproducible peptide synthesis.

Fmoc & tBu Protection – Provides selective deprotection, enabling controlled peptide assembly.

Ideal for Solid-Phase Peptide Synthesis (SPPS) – Prevents side reactions while enabling efficient peptide elongation.

Versatile Applications – Used in protein engineering, drug development, and biochemical studies.

Stable & Well-CharacterizedOptical activity ([α]²⁰/D -5.0±2.0°), HPLC assay (≥98.0%), and low impurity levels (~4% water content) ensure high-quality performance.

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Glu(OtBu)-OH, ≥98.0% (HPLC)
CAS Number71989-18-9
Empirical FormulaC₂₄H₂₇NO₆
Molecular Weight425.47 g/mol
Beilstein Registry Number3636375
EC Number276-253-8
MDL NumberMFCD00037135
PubChem Substance ID57651045
Optical Activity[α]²⁰/D -5.0±2.0° (c = 1% in acetic acid: water (4:1))
FormPowder
Assay (HPLC)≥98.0%
Storage Temperature2-8°C
Functional GroupFmoc
Impurities~4% water
SolubilitySoluble in organic solvents, insoluble in water

Applications

🔹 Peptide Synthesis & Proteomics Research – Used in Fmoc-based SPPS for efficient glutamic acid incorporation.

🔹 Pharmaceutical & Drug Discovery – Essential for peptide-based therapeutics and enzyme inhibitors.

🔹 Bioconjugation & Protein Engineering – Facilitates biomolecule modifications and bioactive compound synthesis.

🔹 Bioorganic Chemistry & Materials Science – Used in biopolymer design and functional material synthesis.

Reported Applications Include:

1️⃣ Ligand in the Synthesis of cis-Substituted Cyclopropane Carboxylic Acids – Used in C-H activation of cyclopropane carboxamides via Pd-catalyzed reactions.

2️⃣ Linker in Multi-Small Molecule-Conjugated PTX (Paclitaxel) Derivatives – Applied in drug conjugation strategies for targeted therapy.

3️⃣ Stapled α-Helical Peptides – Used in stapled peptide design for enhanced bioactivity and stability.

4️⃣ Peptide C-Terminal Thioesters – Employed in native chemical ligation (NCL) for protein semi-synthesis.

Storage & Handling

📦 Storage Conditions:

  • Store at 2-8°C in a dry, tightly sealed container.
  • Keep away from oxidizing agents and moisture to maintain stability.

Handling Precautions:

  • Use in a well-ventilated area.
  • Wear PPE – gloves, lab coat, and safety goggles.
  • Avoid exposure to moisture and direct sunlight.

General References & Research Citations

1️⃣ Ligand in the Synthesis of cis-Substituted Cyclopropane Carboxylic AcidsOrg. Lett., 2013, 15(9), 2179-2182.

2️⃣ Linker in Multi-Small Molecule-Conjugated PTX (Paclitaxel) DerivativesJ. Med. Chem., 2018, 61(11), 4941-4954.

3️⃣ Stapled α-Helical PeptidesNature Chemistry, 2014, 6(7), 614-622.

4️⃣ Peptide C-Terminal ThioestersJ. Am. Chem. Soc., 2012, 134(42), 17714-17721.

Regulatory & Safety Information

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

Hazard Warnings: Follow standard lab safety protocols when handling.

Ordering Information

Catalog NumberQuantity
47625-10G10 g
47625-25G25 g
47625-100G100 g
47625-1KG1 kg

📦 Shipping Conditions: Ambient

Sigma-Aldrich™ Fmoc-Glu(OtBu)-OH (≥98.0%) is a high-purity, selectively protected amino acid essential for solid-phase peptide synthesis (SPPS), pharmaceutical research, and biochemical studies. Its Fmoc and tBu protection enable precise deprotection steps, making it ideal for controlled peptide assembly, protein engineering, and biomedical applications.

  • Pack Size:   1kg 100g 10g 25g


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