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Catalog Number:
12989
CAS Number:
157887-82-6
3-(Fmoc-amino)-1-propanol
Purity:
≥ 99% (HPLC)
Synonym(s):
9-Fluorenyl-methyl N-(3-hydroxypropyl)carbamate
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Product Information

3-(Fmoc-amino)-1-propanol is a versatile compound widely utilized in the field of organic synthesis and peptide chemistry. This amino alcohol serves as a key building block for the synthesis of various peptides and proteins, making it invaluable for researchers in medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protective group allows for selective deprotection, facilitating the stepwise assembly of complex peptide structures. The compound's unique properties, such as its ability to enhance solubility and stability of peptide chains, make it an excellent choice for applications in drug development and therapeutic research.

In addition to its role in peptide synthesis, 3-(Fmoc-amino)-1-propanol is also employed in the development of advanced materials and nanotechnology. Its functional groups can be easily modified, allowing for the creation of tailored compounds with specific properties for targeted applications. Researchers appreciate its compatibility with various coupling reactions, which streamlines the synthesis process and improves overall yield. This compound not only simplifies the workflow in peptide synthesis but also opens new avenues for innovative research in pharmaceuticals and biotechnology.

Synonyms
9-Fluorenyl-methyl N-(3-hydroxypropyl)carbamate
CAS Number
157887-82-6
Purity
≥ 99% (HPLC)
Molecular Formula
C18H19NO3
Molecular Weight
297.35
MDL Number
MFCD00409484
PubChem ID
2736488
Melting Point
127 - 128 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
9-Fluorenyl-methyl N-(3-hydroxypropyl)carbamate
CAS Number
157887-82-6
Purity
≥ 99% (HPLC)
Molecular Formula
C18H19NO3
Molecular Weight
297.35
MDL Number
MFCD00409484
PubChem ID
2736488
Melting Point
127 - 128 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(Fmoc-amino)-1-propanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new therapeutic agents, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs or imaging agents to biomolecules, enhancing their efficacy and specificity.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding in the development of treatments for neurological disorders.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating functional polymers with specific properties for various applications.

Citations