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Catalog Number:
30525
CAS Number:
560088-89-3
Ácido Fmoc-8-amino-3,6-dioxaoctanoil-8-amino-3,6-dioxaoctanoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-AEEA-AEEA, Fmoc-O2Oc-O2Oc-OH
Temperature Sensitive
Documents
$130.00 /250 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-8-amino-3,6-dioxaoctanoyl-8-amino-3,6-dioxaoctanoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure, characterized by multiple ethylene glycol units, enhances solubility and facilitates the formation of stable peptide bonds, making it an excellent choice for researchers focused on bioconjugation and the development of therapeutic peptides.

In practical applications, this compound is particularly valuable in the fields of medicinal chemistry and biotechnology. It is often employed in the synthesis of complex peptides and proteins, enabling the creation of novel therapeutics with improved efficacy and stability. Additionally, its unique properties allow for the development of drug delivery systems that can enhance bioavailability and target specific tissues. Researchers and industry professionals can leverage Fmoc-8-amino-3,6-dioxaoctanoyl-8-amino-3,6-dioxaoctanoic acid to streamline their peptide synthesis processes and improve the overall quality of their pharmaceutical products.

Synonyms
Fmoc-AEEA-AEEA, Fmoc-O2Oc-O2Oc-OH
CAS Number
560088-89-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H34N2O9
Molecular Weight
530.6
MDL Number
MFCD09752868
PubChem ID
51340574
Appearance
Aceite de color amarillo claro o incoloro.
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
Fmoc-AEEA-AEEA, Fmoc-O2Oc-O2Oc-OH
CAS Number
560088-89-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C27H34N2O9
Molecular Weight
530.6
MDL Number
MFCD09752868
PubChem ID
51340574
Appearance
Aceite de color amarillo claro o incoloro.
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-8-amino-3,6-dioxaoctanoyl-8-amino-3,6-dioxaoctanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting others. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of drug candidates that can improve bioavailability and target specificity, particularly in the development of peptide-based therapeutics.
  • Bioconjugation: The compound serves as a linker in bioconjugation processes, facilitating the attachment of drugs to antibodies or other biomolecules, enhancing therapeutic efficacy and reducing side effects.
  • Research in Biochemistry: It is utilized in various biochemical assays and experiments, providing researchers with tools to study protein interactions and enzyme activities, which are essential in understanding biological processes.
  • Nanotechnology: The compound is also explored in the field of nanotechnology for creating functionalized nanoparticles, which can be used in targeted drug delivery systems, improving treatment outcomes in cancer therapy.

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