Fmoc-N-Methyl Amino Acids: High-Purity Building Blocks for Peptide Synthesis
Advanced peptide chemistry and solid-phase peptide synthesis (SPPS) require specialized building blocks to overcome aggregation, improve solubility, and enhance backbone stability. Fmoc-N-Methyl amino acids provide chemical modifications that alter peptide conformation, increase enzymatic resistance, and optimize pharmacokinetic profiles.
Explore our comprehensive catalog of N-methylated building blocks tailored for research laboratories, pharmaceutical development, and chemical synthesis. For additional research compounds and raw materials, browse the selection available at amino asylum.
Why Incorporate Fmoc-N-Methylated Building Blocks?
N-methylation replaces the amide hydrogen on the peptide backbone with a methyl group. This structural modification provides several biochemical advantages:
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Conformational Rigidity: Restricts backbone flexibility, helping stabilize specific active peptide conformations for improved receptor selectivity.
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Proteolytic Stability: Protects peptide bonds against enzymatic cleavage, extending in vivo half-life.
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Preventing Aggregation: Disrupts interchain hydrogen bonding during SPPS, mitigating beta-sheet formation and aggregation during sequence elongation.
Specialized Fmoc-N-Methyl Amino Acid Variants
Understanding where specific N-methylated derivatives fit into your synthetic workflows helps ensure optimal coupling efficiency and target yields:
Sourcing Methylated Intermediates & Reagents
If you are researching where to buy Methyl Amine reagents or specialized amine derivatives to modify building blocks in-house, securing high-purity starting materials is critical for avoiding unwanted side products during coupling steps.
When looking to buy Amino Methyl compounds and Fmoc-protected derivatives online, prioritize suppliers that provide verified purity profiles via HPLC and Mass Spectrometry (MS).
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High Coupling Efficiency: Optimized protecting group strategies prevent side-reactions during deprotection cycles.
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Lab-Verified Purity: Consistent batch-to-batch quality ensures reproducible synthetic outcomes.
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Versatile Compatibility: Fully compatible with standard Fmoc/tBu SPPS protocols and automated peptide synthesizers.
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-MeNle-OH
- Catalog Number FL2372 Chemical Structure CAS Number 112883-42-8 Molecular Weight 367.43g/mole Formula C22H25NO4
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-MeOrn(Aloc)-OH
- Catalog Number FO2593 Chemical Structure Molecular Weight 452.48g/mole Formula C25H28N2O6
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Aib-OH
- Catalog Number FX2666 Chemical Structure CAS Number 400779-65-9 Molecular Weight 339.39 g/mol Formula C20H21NO4 Synonym Fmoc-N,2-dimethylalanine; Fmoc-α-(methylamino)isobutyric acid
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Ala-OH
- Catalog Number FA2102 Chemical Structure CAS Number 84000-07-7 Molecular Weight 325.36g/mole Formula C19H19NO4
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Arg(Pbf)-OH
- Catalog Number FR2161 Chemical Structure CAS Number 913733-27-4 Molecular Weight 662.80 g/mole Formula C34H40N4O7S
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- Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Asn(Trt)-OH
- Catalog Number FN2161 Chemical Structure CAS Number 941296-80-6 Molecular Weight 610.70 g/mole Formula C39H34N2O5
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Asp(OtBu)-OH
- Catalog Number FD2161 Chemical Structure CAS Number 152548-66-8 Molecular Weight 425.47 g/mole Formula C24H27NO6
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- Fmoc-N-Methyl Amino Acids, AMINOS
Fmoc-N-Me-Cys(Trt)-OH
- Catalog Number FC2161 Chemical Structure CAS Number 944797-51-7 Molecular Weight 599.74 g/mole Formula C38H33NO4S
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Gln(Trt)-OH
- Catalog Number FQ2161 Chemical Structure CAS Number 1632075-13-8 Molecular Weight 624.72 g/mole Formula C40H36N2O5
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Glu(OtBu)-OH
- Catalog Number FE2161 Chemical Structure CAS Number 200616-40-6 Molecular Weight 439.50 g/mole Formula C25H29NO6
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-His(Trt)-OH
- Catalog Number FH2161 Chemical Structure CAS Number 1217840-61-3 Molecular Weight 633.73 g/mole Formula C41H35N3O4
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Ile-OH
- Catalog Number FI2327 Chemical Structure CAS Number 138775-22-1 Molecular Weight 367.44g/mole Formula C22H25NO4
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Leu-OH – An N-Fmoc-N-methyl amino acid
- Catalog Number FL2352 PubChem CID 7015835 Mass 367.17835828 Chemical Formula C₂₂H₂₅NO₄ Isomeric SMILES CC(C)C[C@@H](C(=O)O)N(C)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13 DSSTox Substance ID DTXSID70426778 CAS Registry Number 103478-62-2 SureChEMBL ID 1486163 Stereoisomer Of Fmoc-N-methyl-D-leucine UniChem Compound ID 23806570 InChIKey BUJQSIPFDWLNDC-FQEVSTJZSA-N Subclass Of chemical compound Instance Of type of chemical entity InChI InChI=1S/C22H25NO4/c1-14(2)12-20(21(24)25)23(3)22(26)27-13-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,14,19-20H,12-13H2,1-3H3,(H,24,25)/t20-/m0/s1 Canonical SMILES CC(C)CC(C(=O)O)N(C)C(=O)OCC1c2ccccc2-c2ccccc21 Probes And Drugs ID PD099511 DSSTOX Compound Identifier DTXCID90377612
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Lys(Boc)-OH
- Catalog Number FK2161 Chemical Structure CAS Number 197632-76-1 Molecular Weight 482.57 g/mole Formula C27H34N2O6
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- AMINOS, Fmoc-N-Methyl Amino Acids
Fmoc-N-Me-Lys(ivDde)-OH
- Catalog Number FK2162 Chemical Structure CAS Number 1173996-67-2 Molecular Weight 588.73 g/mole Formula C35H44N2O6 Synonym N2-Fmoc-N6-ivDde-N2-methyl-L-lysine
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