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Catalog Number:
12959
CAS Number:
127903-20-2
6-(Fmoc-amino)-1-hexanol
Purity:
≥ 98% (HPLC)
Synonym(s):
9-Fluorenylmethyl N-(6-hydroxyhexyl)carbamate, 6-Fmoc-Acp-ol
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Product Information

6-(Fmoc-amino)-1-hexanol is a versatile compound widely utilized in the field of organic chemistry, particularly in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for the efficient coupling with various amino acids, making it an invaluable tool for researchers aiming to create complex peptide sequences. The hydroxyl group in its structure enhances its reactivity, enabling the formation of various derivatives that can be tailored for specific applications in medicinal chemistry.

In addition to its role in peptide synthesis, 6-(Fmoc-amino)-1-hexanol has potential applications in the development of drug delivery systems and biomaterials. Its hydrophobic hexanol chain can improve the solubility and stability of therapeutic agents, while the Fmoc group facilitates easy deprotection under mild conditions. This compound stands out for its ability to streamline the synthesis process, reduce side reactions, and enhance the overall yield of desired products, making it a preferred choice for professionals in pharmaceutical and biotechnological research.

Synonyms
9-Fluorenylmethyl N-(6-hydroxyhexyl)carbamate, 6-Fmoc-Acp-ol
CAS Number
127903-20-2
Purity
≥ 98% (HPLC)
Molecular Formula
C21H25NO3
Molecular Weight
339.43
MDL Number
MFCD00380196
PubChem ID
2736486
Melting Point
134-137 ?C
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
9-Fluorenylmethyl N-(6-hydroxyhexyl)carbamate, 6-Fmoc-Acp-ol
CAS Number
127903-20-2
Purity
≥ 98% (HPLC)
Molecular Formula
C21H25NO3
Molecular Weight
339.43
MDL Number
MFCD00380196
PubChem ID
2736486
Melting Point
134-137 ?C
Appearance
White to off-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

6-(Fmoc-amino)-1-hexanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of drug candidates, particularly in creating compounds with improved solubility and bioavailability, which is crucial for effective therapeutic agents.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Material Science: In the field of material science, it is employed to modify polymers, improving their properties for applications in coatings, adhesives, and other materials.
  • Research in Organic Chemistry: This compound is frequently used in organic synthesis as a versatile building block, facilitating the creation of complex molecules with diverse applications in various chemical industries.

Citations