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Sigma-Aldrich™ Fmoc-Val-OH, ≥98.0% (HPLC)

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SKU: 47638-250G-F
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-Val-OH, also known as Fmoc-L-Valine, is a high-purity, N-protected amino acid derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group, allowing selective deprotection and controlled stepwise peptide elongation.

Valine is a branched-chain hydrophobic amino acid that contributes to protein folding, peptide stability, hydrophobic interactions, and secondary structure formation. Fmoc-Val-OH is therefore an important building block for custom peptide synthesis, pharmaceutical research, drug discovery, proteomics, enzyme-substrate studies, protein engineering, and bioconjugation applications.

Key Features

FeatureDetails
High Purity≥98.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Valine Building BlockEnables incorporation of valine residues into synthetic peptides
Hydrophobic Amino AcidSupports peptide folding, protein stability, and hydrophobic interactions
SPPS CompatibleSuitable for solid-phase peptide synthesis and peptide modification
Research ApplicationsIdeal for peptide chemistry, pharmaceutical research, proteomics, and protein engineering

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Val-OH, ≥98.0% HPLC
SynonymFmoc-L-Valine
CAS Number68858-20-8
Empirical FormulaC₂₀H₂₁NO₄
Molecular Weight339.39 g/mol
Beilstein Registry Number2177443
EC Number272-515-0
MDL NumberMFCD00037124
PubChem Substance ID57651055
Optical Activity[α]²⁰/D -17 ± 1°; c = 1% in DMF
FormSolid
Melting Point143–147 °C
Assay≥98.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, carboxylic acid

Applications

Fmoc-Val-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of valine 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
  • Proteomics and biochemical research
  • Bioconjugation and functionalized peptide synthesis
  • Studies involving hydrophobic peptide regions and protein stability

Ordering Information

Catalog NumberQuantity
47638-50G-F50 g
47638-250G-F250 g

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, light, 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-Val-OH, also known as Fmoc-L-Valine, is a high-purity, N-protected amino acid derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group, allowing selective deprotection and controlled stepwise peptide elongation.

Valine is a branched-chain hydrophobic amino acid that contributes to protein folding, peptide stability, hydrophobic interactions, and secondary structure formation. Fmoc-Val-OH is therefore an important building block for custom peptide synthesis, pharmaceutical research, drug discovery, proteomics, enzyme-substrate studies, protein engineering, and bioconjugation applications.

Key Features

FeatureDetails
High Purity≥98.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Valine Building BlockEnables incorporation of valine residues into synthetic peptides
Hydrophobic Amino AcidSupports peptide folding, protein stability, and hydrophobic interactions
SPPS CompatibleSuitable for solid-phase peptide synthesis and peptide modification
Research ApplicationsIdeal for peptide chemistry, pharmaceutical research, proteomics, and protein engineering

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Val-OH, ≥98.0% HPLC
SynonymFmoc-L-Valine
CAS Number68858-20-8
Empirical FormulaC₂₀H₂₁NO₄
Molecular Weight339.39 g/mol
Beilstein Registry Number2177443
EC Number272-515-0
MDL NumberMFCD00037124
PubChem Substance ID57651055
Optical Activity[α]²⁰/D -17 ± 1°; c = 1% in DMF
FormSolid
Melting Point143–147 °C
Assay≥98.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, carboxylic acid

Applications

Fmoc-Val-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of valine 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
  • Proteomics and biochemical research
  • Bioconjugation and functionalized peptide synthesis
  • Studies involving hydrophobic peptide regions and protein stability

Ordering Information

Catalog NumberQuantity
47638-50G-F50 g
47638-250G-F250 g

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, light, 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-Val-OH, also known as Fmoc-L-Valine, is a high-purity, N-protected amino acid derivative used in Fmoc-based solid-phase peptide synthesis (SPPS). It features an Fmoc-protected α-amino group, allowing selective deprotection and controlled stepwise peptide elongation.

Valine is a branched-chain hydrophobic amino acid that contributes to protein folding, peptide stability, hydrophobic interactions, and secondary structure formation. Fmoc-Val-OH is therefore an important building block for custom peptide synthesis, pharmaceutical research, drug discovery, proteomics, enzyme-substrate studies, protein engineering, and bioconjugation applications.

Key Features

FeatureDetails
High Purity≥98.0% by HPLC for reliable peptide synthesis
Fmoc ProtectionProtects the α-amino group for controlled Fmoc-SPPS workflows
Valine Building BlockEnables incorporation of valine residues into synthetic peptides
Hydrophobic Amino AcidSupports peptide folding, protein stability, and hydrophobic interactions
SPPS CompatibleSuitable for solid-phase peptide synthesis and peptide modification
Research ApplicationsIdeal for peptide chemistry, pharmaceutical research, proteomics, and protein engineering

Chemical Properties & Identifiers

PropertyValue
Product NameFmoc-Val-OH, ≥98.0% HPLC
SynonymFmoc-L-Valine
CAS Number68858-20-8
Empirical FormulaC₂₀H₂₁NO₄
Molecular Weight339.39 g/mol
Beilstein Registry Number2177443
EC Number272-515-0
MDL NumberMFCD00037124
PubChem Substance ID57651055
Optical Activity[α]²⁰/D -17 ± 1°; c = 1% in DMF
FormSolid
Melting Point143–147 °C
Assay≥98.0% by HPLC
Storage Temperature2–8 °C
Functional GroupsFmoc, amine, carboxylic acid

Applications

Fmoc-Val-OH is suitable for:

  • Fmoc-based solid-phase peptide synthesis
  • Incorporation of valine 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
  • Proteomics and biochemical research
  • Bioconjugation and functionalized peptide synthesis
  • Studies involving hydrophobic peptide regions and protein stability

Ordering Information

Catalog NumberQuantity
47638-50G-F50 g
47638-250G-F250 g

Storage & Handling

Store at 2–8 °C in a dry, tightly sealed container. Protect from moisture, light, 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 250g, 50g