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Catalog Number:
22671
CAS Number:
756525-91-4
Boc-15-amino-4,7,10,13-tetraoxapentadecanoic acid
Purity:
≥ 95%
Synonym(s):
15-(Boc-amino)-4,7,10,13-tetraoxapentadecanoic acid, Boc-NH-(PEG)3-COOH
Documents
$113.87 /250MG
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Product Information

Boc-15-amino-4,7,10,13-tetraoxapentadecanoic acid is a versatile compound widely recognized for its applications in peptide synthesis and drug development. This amino acid derivative features a unique Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its structure, characterized by multiple ethylene glycol units, allows for improved solubility and bioavailability, which is crucial for pharmaceutical formulations.

In practical applications, Boc-15-amino-4,7,10,13-tetraoxapentadecanoic acid is utilized in the synthesis of complex peptides and proteins, facilitating the development of therapeutic agents. Its ability to form stable linkages with other biomolecules opens avenues for creating targeted drug delivery systems and enhancing the efficacy of therapeutic compounds. Researchers appreciate its compatibility with various coupling reagents, which streamlines the synthesis process, ultimately leading to more efficient and cost-effective production of bioactive molecules.

Synonyms
15-(Boc-amino)-4,7,10,13-tetraoxapentadecanoic acid, Boc-NH-(PEG)3-COOH
CAS Number
756525-91-4
Purity
≥ 95%
Molecular Formula
C16H31NO8
Molecular Weight
365.42
MDL Number
MFCD07781254
PubChem ID
2756001
Appearance
Yellow oil or colorless syrup
Conditions
Store at 0-8 °C
General Information
Synonyms
15-(Boc-amino)-4,7,10,13-tetraoxapentadecanoic acid, Boc-NH-(PEG)3-COOH
CAS Number
756525-91-4
Purity
≥ 95%
Molecular Formula
C16H31NO8
Molecular Weight
365.42
MDL Number
MFCD07781254
PubChem ID
2756001
Appearance
Yellow oil or colorless syrup
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

Boc-15-amino-4,7,10,13-tetraoxapentadecanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of drug candidates, particularly in enhancing solubility and bioavailability. Researchers can leverage its properties to develop more effective therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes, which involve attaching biomolecules to drugs or imaging agents. This application is vital in creating targeted therapies and diagnostic tools.
  • Polymer Chemistry: It can be incorporated into polymeric materials to modify their properties, such as increasing hydrophilicity or biocompatibility, making it useful in biomedical applications like drug delivery systems.
  • Research in Nanotechnology: The compound's functional groups can facilitate the formation of nanocarriers for drug delivery, improving the efficiency of treatments while minimizing side effects.

Citations