Metabolic Regulation Peptides Bioactive Toxin-Derived Peptides Tumor-Associated Antigen Peptides Nuclear Localization Signals (NLS) Cell-Penetrating Peptides (CPPs) Neurodegenerative Disease Research Peptides Melanogenesis Modulation Anti-Aging & Skin Remodeling Gastrin, GRP & Bombesin Peptides Somatostatin Analogs DPPIV/CD26 Peptides Kinase Activity Modulators Caspase Substrates & Inhibitors Viral Protease Substrates Antiviral Peptides Antimicrobial Peptides Cardiovascular Peptides Immunomodulatory Peptides Calcitonin & CGRP Family Peptides Incretin & Metabolic Peptides Parathyroid Hormone (PTH) Growth Hormone GnRH Analogues/Antagonists Pain and Inflammation Modulation Pituitary Hormones Neurotransmitters/Neuropeptides Standard Fmoc-Amino Acids D-Form Amino Acids Resins Peptide Synthesis Reagents & Additives Specialty Peptide Building Blocks Pseudoproline Dipeptides Phenylalanine & Tryptophan Unusual Amino Acids & Analogs Newly Launched Small-Molecule Specialties Impurity Analysis & Bioactivity Research Special Offers Peptide Synthesis Chemical Synthesis ADMET Profiling Service AlanMolecularAI AlanDockAI Linear Peptide Optimization Cyclic Peptide Optimization Task Management Knowledge Center News About Us Reagents & Custom Orders Aipower Platform
Sign in
Cart
Search
Home Product Protected Amino Acids, Resins & Reagents Specialty Peptide Building Blocks Fmoc-Val-Val-Val-OH

DESCRIPTION

Fmoc-Val-Val-Val-OH is a preassembled trivaline fragment with an Fmoc-protected N-terminus and free C-terminal carboxyl.

Three consecutive β-branched valines create a strongly hydrophobic, sterically crowded sequence environment. For a shorter related fragment, compare Fmoc-Leu-Val-OH or Fmoc-Phe-Val-OH depending on the intended N-terminal residue.

Product Information

Product NameFmoc-Val-Val-Val-OH
Catalog No.AS4148
CAS No.649757-37-9
Molecular FormulaC30H39N3O6
Molecular Weight537.66 g/mol
Material / Building Block TypeFmoc-protected Val-Val-Val tripeptide fragment
Primary ApplicationsHydrophobic peptide fragment synthesis; β-branched motif assembly; aggregation-prone sequence research; convergent peptide synthesis

Application Scope in Hydrophobic Sequence Assembly

Val-rich segments are used in peptide SAR, structural motifs and hydrophobic-core models. A preformed Val3 fragment can be useful when repeated stepwise coupling of β-branched Val becomes inefficient.

Aggregation and Coupling Behavior

Consecutive Val residues can promote resin aggregation and difficult coupling because each residue is β-branched. Fragment incorporation reduces some downstream coupling cycles but the terminal Val junction can still be sterically demanding.

Procurement and QC

Confirm CAS 649757-37-9, C30H39N3O6, MW 537.66 g/mol and Val-Val-Val sequence identity. HPLC/MS should be reviewed for deletion or chain-length impurities.

For highly hydrophobic or aggregation-prone sequences, Alan Scientific can optimize assembly through custom peptide synthesis.

Product Documents

A Safety Data Sheet (SDS / MSDS) is available for this product to support laboratory handling, storage and safety assessment.

Fmoc-Val-Val-Val-OH MSDS

Certificates of Analysis (COAs) are batch-specific. Please contact us to request the COA for your product, and we will provide it by email.

Frequently Asked Questions

Why can Val3 be difficult to synthesize stepwise?

Consecutive β-branched residues increase steric hindrance and can promote aggregation.

Is the C-terminal carboxyl free?

Yes.

Does a preformed fragment eliminate all coupling difficulty?

No. The fragment-to-chain junction may still be demanding.

Related Technical Resources

Research Use Only.

Fmoc-Val-Val-Val-OH

Catalog No: AS4148
Cas No: 649757-37-9

{{ getShowPrice() }} {{ getPrice() }}

Add to Cart Bulk Inquiry
{{ isCollect ? 'Cancel collection' : 'Collection' }}

Related Products

Submit