FMOC-NIP-OH

≥97%

Reagent Code: #86916
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CAS Number 158922-07-7

science Other reagents with same CAS 158922-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.4 g/mol
Formula C₂₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD00673789
thermostat Physical Properties
Boiling Point 561.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.293 g/cm3
Storage 2-8°C

description Product Description

FMOC-NIP-OH is an Fmoc-protected derivative of NIP-OH, primarily used in peptide synthesis. The FMOC (9-fluorenylmethoxycarbonyl) group acts as a protecting group for the amino terminus of the amino acid, enabling the stepwise construction of peptides by preventing unwanted reactions at specific sites. It is commonly employed in solid-phase peptide synthesis (SPPS) to ensure high purity and yield of the final peptide product. Its stability under various reaction conditions makes it a reliable choice for complex peptide assembly. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid sequences is critical.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,152.00
inventory 5g
10-20 days ฿4,608.00
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FMOC-NIP-OH
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FMOC-NIP-OH is an Fmoc-protected derivative of NIP-OH, primarily used in peptide synthesis. The FMOC (9-fluorenylmethoxycarbonyl) group acts as a protecting group for the amino terminus of the amino acid, enabling the stepwise construction of peptides by preventing unwanted reactions at specific sites. It is commonly employed in solid-phase peptide synthesis (SPPS) to ensure high purity and yield of the final peptide product. Its stability under various reaction conditions makes it a reliable choice for

FMOC-NIP-OH is an Fmoc-protected derivative of NIP-OH, primarily used in peptide synthesis. The FMOC (9-fluorenylmethoxycarbonyl) group acts as a protecting group for the amino terminus of the amino acid, enabling the stepwise construction of peptides by preventing unwanted reactions at specific sites. It is commonly employed in solid-phase peptide synthesis (SPPS) to ensure high purity and yield of the final peptide product. Its stability under various reaction conditions makes it a reliable choice for complex peptide assembly. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise control over amino acid sequences is critical.

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