117048-49-4

Basic information

• Product Name: FMOC-NH(CH2)4NH2 HCL
• Synonyms: N1-(9-FLUORENYLMETHYLOXYCARBONYL)-1,4-DIAMINOBUTANE HYDROCHLORIDE;N-1-(9-FLUORENYLMETHOXYCARBONYL)-1,4-DIAMINOBUTANE HCL;N-(9-FLUORENYLMETHYLOXYCARBONYL)-1,4-DIAMINOBUTANE HYDROCHLORIDE;FMOC-NH(CH2)4NH2 HCL;FMOC-PUTRESCINE;FMOC-DAB HCL;FMOC-DIAMINOBUTANE HCL;FMOC-DIAMINOBUTANE HYDROCHLORIDE
• CAS NO: 117048-49-4
• Molecular Formula: C19H23ClN2O2
• Molecular Weight: 346.85
• Mol File: 117048-49-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Density: 1.158
• Storage Temp.: 2-8°C
• CAS DataBase Reference: FMOC-NH(CH2)4NH2 HCL(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-NH(CH2)4NH2 HCL(117048-49-4)
• EPA Substance Registry System: FMOC-NH(CH2)4NH2 HCL(117048-49-4)

Safety Data

• Hazardous Substances Data: 117048-49-4(Hazardous Substances Data)

Usage

Description

FMOC-NH(CH2)4NH2 HCL is a chemical compound that features a fluorescent moiety (FMOC) attached to a primary amine, which is connected to a four-carbon chain. This results in a positively charged compound in the form of a hydrochloride salt. Known for its fluorescent properties, it is widely utilized in various applications across chemical and biological research.

Uses

Used in Solid-Phase Peptide Synthesis:
FMOC-NH(CH2)4NH2 HCL is used as a protecting group in solid-phase peptide synthesis for the selective protection of primary amines. Its fluorescent properties allow for easy monitoring of the synthesis process and the detection of the protected amine.
Used in Labeling Amino Acids and Peptides:
In the field of biochemistry, FMOC-NH(CH2)4NH2 HCL is used as a labeling reagent for amino acids and peptides. The fluorescent tag enables the tracking and detection of these biomolecules in various assays and experiments.
Used in the Development of Peptide-Based Bioconjugates:
FMOC-NH(CH2)4NH2 HCL is employed as a component in the creation of peptide-based bioconjugates. The fluorescent moiety allows for the visualization and analysis of these conjugates in biological systems.
Used in Fluorescent Probes for Biological Imaging:
In the field of molecular biology, FMOC-NH(CH2)4NH2 HCL is used in the development of fluorescent probes for biological imaging. FMOC-NH(CH2)4NH2 HCL's fluorescent properties facilitate the observation of cellular processes and interactions at the molecular level.
Used in Antimicrobial Research:
FMOC-NH(CH2)4NH2 HCL has been studied for its potential antimicrobial properties. It is used as a candidate compound in the search for new antimicrobial agents to combat resistant bacteria.
Used in Anticancer Research:
In oncology, FMOC-NH(CH2)4NH2 HCL is explored for its potential anticancer properties. It is used as a candidate compound in the development of new cancer therapies, with the aim of identifying its effects on cancer cells and its potential synergistic effects with existing treatments.
Used in Chemical and Biological Research Applications:
FMOC-NH(CH2)4NH2 HCL is a versatile compound used across various chemical and biological research applications. Its fluorescent and chemical properties make it a valuable tool for the development of new methodologies, assays, and analytical techniques.