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Catalog Number:
22673
CAS Number:
867062-95-1
Fmoc-12-amino-4,7,10-trioxadodecanoic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-NH-(PEG)3-CH2CH2COOH
Temperature Sensitive
Documents
$86.23 /250MG
Pack Size Availability Price
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Product Information

Fmoc-12-amino-4,7,10-trioxadodecanoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a unique trioxadodecanoic acid backbone, which enhances its solubility and stability in various solvents, making it an ideal choice for researchers working in organic chemistry and biochemistry. The Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides and proteins.

Its application extends to the development of bioconjugates and drug delivery systems, where the compound's structural properties can be leveraged to improve the efficacy and targeting of therapeutic agents. Researchers have found that the incorporation of Fmoc-12-amino-4,7,10-trioxadodecanoic acid into peptide sequences can enhance biological activity and stability, making it a valuable tool in pharmaceutical research and development. This compound stands out for its ability to provide a balance between hydrophilicity and hydrophobicity, which is crucial for optimizing drug formulations.

Synonyms
Fmoc-NH-(PEG)3-CH2CH2COOH
CAS Number
867062-95-1
Purity
≥ 97% (HPLC)
Molecular Formula
C24H29NO7
Molecular Weight
443.5
MDL Number
MFCD06656471
PubChem ID
2756185
Appearance
White powder or viscous liquid
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-NH-(PEG)3-CH2CH2COOH
CAS Number
867062-95-1
Purity
≥ 97% (HPLC)
Molecular Formula
C24H29NO7
Molecular Weight
443.5
MDL Number
MFCD06656471
PubChem ID
2756185
Appearance
White powder or viscous liquid
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-12-amino-4,7,10-trioxadodecanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it aids in the design of drug candidates by facilitating the incorporation of amino acids into larger molecular frameworks, enhancing bioavailability and efficacy.
  • Bioconjugation: The compound is useful in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the performance of diagnostic tools and therapeutics.
  • Polymer Chemistry: It finds applications in the development of functional polymers, contributing to materials with specific properties for use in coatings, adhesives, and biomedical devices.
  • Research in Nanotechnology: This chemical plays a role in the fabrication of nanomaterials, where its unique structure can be exploited to create nanoscale devices with enhanced functionality.

Citations