A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Fmoc-4,5-dehydro-L-leucine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-4-(7-hydroxycoumarin-4-yl)-Abu-OH
Fmoc-4-(7-hydroxycoumarin-4-yl)-Abu-OH is a protected derivative of the fluorescent amino acid Cgl and a homolog of the coumarinylalanine derivative Fmoc-β-(7-methoxycoumarin-4-yl)-Ala-OH. Synonyms: Fmoc-(7-hydroxycoumarin-4-yl)-ethyl-Gly-OH; (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(7-hydroxy-2-oxo-2H-chromen-4-yl)butanoic acid; FMoc-(umbellifer-4-yl)-ethyl-Gly-OH; 2H-1-Benzopyran-4-butanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-7-hydroxy-2-oxo-, (αS)-. Grade: ≥95%. CAS No. 1187744-84-8. Molecular formula: C28H23NO7. Mole weight: 485.49.
Fmoc-4-Amb-Wang resin
Excellent resin for the synthesis of peptide acids using Fmoc strategy. Cleavage can be effected by 95% TFA.
Fmoc-4-amino-(1-carboxymethyl) piperidine
2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid is a synthetic compound designed as a scaffold for drug discovery. It is commonly referred to as Fmoc-Lys(Dde)-OH in the research community. The compound contains one Lysine (Lys) residue, and the abbreviation Dde stands for the protection group used to prevent the Lysine side chain from reacting during peptide synthesis. Uses: The versatility of fmoc-lys(dde)-oh has led to its use in various scientific experiments, including peptide synthesis, drug discovery, and chemical biology. peptides and peptidomimetics containing fmoc-lys(dde)-oh have been used as probes for studying protein-protein interactions, enzyme kinetics, and receptor-ligand binding. Additional or Alternative Names: 2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid, Fmoc-Lys(Dde)-OH. Product Category: Amino Acids. CAS No. 221352-82-5. Molecular formula: C22H24N2O4. Mole weight: 380.4. Purity: Peak Area by HPLC ≥95%. IUPACName: 2-[4-(9H-fluoren-9-ylmethoxycarbonylamino)piperidin-1-yl]acetic acid. Canonical SMILES: C1CN(CCC1NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)CC(=O)O. Density: 1.323 g/cm3. Product ID: ACM221352825-1. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-4-amino-1-carboxy methyl piperidine
Fmoc-4-amino-1-carboxy methyl piperidine. Group: Biochemicals. Grades: Highly Purified. CAS No. 221352-82-5. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Fmoc-4-amino-3,3-dimethyl-butyric acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences.
Worldwide
Fmoc-4-amino-3-hydroxybutanoic acid
Fmoc-4-amino-3-hydroxybutanoic acid (Fmoc-Ahb-OH) is a type of amino acid that contains both an amino group and a carboxyl group. It is commonly used as a building block for peptides, which are short chains of amino acids linked by peptide bonds. Uses: Fmoc-ahb-oh is widely used in the synthesis of peptides for various scientific applications. the inclusion of ahb-oh in peptide chains can result in improved bioactivity or stability of the peptides. for example, ahb-oh can be used to add hydrophilic or amphiphilic characters to peptides, which can enhance their solubility or cell penetration. ahb-oh can also be used to introduce functional groups that can be used for further modification of the peptide. Product Category: Amino Acids. CAS No. 184763-08-4. Molecular formula: C19H19NO5. Mole weight: 341.4. Purity: Peak Area by HPLC ≥95%. IUPACName: 4-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxybutanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCC(CC(=O)O)O. Product ID: ACM184763084. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-4-amino-4-methyl-pentanoic acid 99+% (HPLC)
Fmoc-4-amino-4-methyl-pentanoic acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences.
Fmoc-4-azido-L-phenylalanine. Group: Biochemicals. Alternative Names: Fmoc-L-Phe(4-azido)-OH; Fmoc-p-azido-L-Phe-OH; (S)-Fmoc-2-amino-3-(4-azidophenyl)propionic acid. Grades: Highly Purified. CAS No. 163217-43-4. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Fmoc-4-azido-L-phenylalanine 98+% (TLC)
Fmoc-4-azido-L-phenylalanine 98+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Fmoc-4-azidophenylalanine
Fmoc-4-azido-L-phenylalanine is a compound used in peptide synthesis as a non-natural amino acid due to its unique properties. It is an azido derivative of the amino acid phenylalanine, with an Fmoc (fluorenylmethoxycarbonyl) group protecting its amine function. The azido group can react with alkenes or alkynes via Huisgen 1,3-dipolar cycloaddition, also known as click chemistry, to generate stable triazole linkages. This reaction allows for the creation of complex peptide structures with high efficiency and yield. Uses: Fmoc-4-azido-l-phenylalanine is used as a building block in peptide synthesis to create peptides with specific properties and functions. it has been used to create membrane-active peptides, bioconjugates, and enzyme inhibitors, among other things. Additional or Alternative Names: FMOC-P-AZIDO-L-PHE-OH, Fmoc-L-4-azidophenylalanine, FMOC-PHE(N3)-OH, Fmoc-L-4-azidophe, Fmoc-Phe(4-N3)-OH. Product Category: Amino Acids. CAS No. 163217-43-4. Molecular formula: C24H20N4O4. Mole weight: 428.4. Purity: ≥ 98% (HPLC). IUPACName: (2S)-3-(4-azidophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC=C(C=C4)N=[N+]=[N-])C(=O)O. Product ID: ACM163217434-1. Alfa Chemistry ISO 9001:2015 Certified.
Fmoc-D-Bpa-OH, or N-[(9-fluorenylmethoxycarbonyl)-2-(4'-borono)phenyl]alanine, is a modified amino acid that has a boron atom and a fluorenylmethoxycarbonyl (Fmoc) group attached to the phenylalanine residue. First synthesized by Sheppard et al. in 1993, Fmoc-D-Bpa-OH has been widely used as a non-natural amino acid in peptide chemistry and as a tool in protein engineering and biophysical studies. Uses: Fmoc-d-bpa-oh has various potential applications in diverse fields, including peptide chemistry, protein engineering, and biophysical studies. in peptide chemistry, fmoc-d-bpa-oh can be used as a non-natural amino acid to introduce chemical diversity into peptide sequences, which can then be used for various applications such as drug design and development. in protein engineering, fmoc-d-bpa-oh can be used to introduce non-natural amino acids into proteins, which can then be used to modulate protein activity and stability. Product Category: Amino Acids. CAS No. 117666-97-4. Molecular formula: C31H25NO5. Mole weight: 491.5. Purity: Peak Area by HPLC ≥95%. IUPACName: (2R)-3-(4-benzoylphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Density: 1.3±0.1 g/cm3. Product ID: ACM117666974-1. Alfa Chemistry ISO 9001:2015 Certified.