3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(propyl)amino)propanoic acid

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Reagent Code: #196985
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CAS Number 2171909-89-8

science Other reagents with same CAS 2171909-89-8

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides excellent stability during coupling reactions while allowing selective deprotection under mild basic conditions, typically with piperidine. This makes it ideal for solid-phase peptide synthesis (SPPS), where controlled stepwise assembly of amino acids is required. Its carboxylic acid functionality enables efficient activation and amide bond formation with incoming amino acids. Commonly employed in the preparation of complex peptides, peptidomimetics, and bioconjugates for pharmaceutical and biochemical research. Also useful in the development of functionalized polymers and smart materials due to its well-defined reactivity and compatibility with various linkers and resins.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,240.00
inventory 100mg
10-20 days ฿16,280.00
inventory 250mg
10-20 days ฿26,040.00
inventory 1g
10-20 days ฿64,860.00

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3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(propyl)amino)propanoic acid
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Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides excellent stability during coupling reactions while allowing selective deprotection under mild basic conditions, typically with piperidine. This makes it ideal for solid-phase peptide synthesis (SPPS), where controlled stepwise assembly of amino acids is required. Its carboxylic acid functionality enables efficient activation and amide bond formation with incoming amino acids. Commonly employed in the prepa

Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides excellent stability during coupling reactions while allowing selective deprotection under mild basic conditions, typically with piperidine. This makes it ideal for solid-phase peptide synthesis (SPPS), where controlled stepwise assembly of amino acids is required. Its carboxylic acid functionality enables efficient activation and amide bond formation with incoming amino acids. Commonly employed in the preparation of complex peptides, peptidomimetics, and bioconjugates for pharmaceutical and biochemical research. Also useful in the development of functionalized polymers and smart materials due to its well-defined reactivity and compatibility with various linkers and resins.

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