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Catalog Number:
15086
CAS Number:
868599-73-9
Fmoc-1-amino-3,6-dioxa-8-octanamine hydrochloride
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-1-amino-3,6-dioxa-octane-1,8-diamine hydrochloride, Fmoc-DOOA·HCl
Documents
$72.31 /250MG
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Product Information

Fmoc-1-amino-3,6-dioxa-8-octanamine hydrochloride is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique structure that incorporates both amine and ether functionalities, making it particularly valuable for researchers in medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides and other biomolecules.

In practical applications, Fmoc-1-amino-3,6-dioxa-8-octanamine hydrochloride is employed in the development of pharmaceuticals, particularly in the design of peptide-based drugs that target specific biological pathways. Its ability to enhance solubility and stability of peptide chains makes it an essential tool for researchers aiming to optimize drug formulations. Additionally, this compound's favorable properties can lead to improved bioavailability and efficacy of therapeutic agents, making it a preferred choice for professionals in the pharmaceutical industry.

Synonyms
Fmoc-1-amino-3,6-dioxa-octane-1,8-diamine hydrochloride, Fmoc-DOOA·HCl
CAS Number
868599-73-9
Purity
≥ 97% (HPLC)
Molecular Formula
C21H26N2O4 · HCl
Molecular Weight
406.91
MDL Number
MFCD04112696
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-1-amino-3,6-dioxa-octane-1,8-diamine hydrochloride, Fmoc-DOOA·HCl
CAS Number
868599-73-9
Purity
≥ 97% (HPLC)
Molecular Formula
C21H26N2O4 · HCl
Molecular Weight
406.91
MDL Number
MFCD04112696
Appearance
White crystalline 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

Fmoc-1-amino-3,6-dioxa-8-octanamine hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and improving yield and purity.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating compounds with improved solubility and bioavailability.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Material Science: It is applied in the development of smart materials, contributing to innovations in drug delivery systems and responsive polymers.
  • Research in Biochemistry: This compound aids in studying protein interactions and enzyme activity, providing insights into biological processes and disease mechanisms.

Citations