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Catalog Number:
07315
CAS Number:
164470-64-8
Fmoc-(4-aminomethyl) benzoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-4-Amb-OH
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Product Information

Fmoc-(4-aminomethyl) benzoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process and facilitates selective deprotection. Its unique structure allows for efficient coupling reactions, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry.

In addition to its role in peptide synthesis, Fmoc-(4-aminomethyl) benzoic acid can be employed in the development of advanced materials and pharmaceuticals. Its ability to enhance solubility and improve the pharmacokinetic properties of drug candidates makes it a valuable asset in the pharmaceutical industry. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in generating high-purity peptides, which are crucial for therapeutic applications. With its robust performance and adaptability, this compound stands out as a key player in modern chemical research and development.

Synonyms
Fmoc-4-Amb-OH
CAS Number
164470-64-8
Purity
≥ 98% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.41
MDL Number
MFCD01074693
PubChem ID
2756083
Appearance
White Powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-4-Amb-OH
CAS Number
164470-64-8
Purity
≥ 98% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.41
MDL Number
MFCD01074693
PubChem ID
2756083
Appearance
White Powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(4-aminomethyl) benzoic acid 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 without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it aids in the design of drug candidates by modifying amino acids, enhancing their bioavailability and therapeutic efficacy. This is crucial for developing effective treatments.
  • Bioconjugation: The compound is used to attach biomolecules to surfaces or other molecules, facilitating the creation of targeted drug delivery systems and improving the specificity of therapeutic agents.
  • Material Science: It finds applications in creating functional materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine, providing scaffolds that mimic natural tissues.
  • Analytical Chemistry: Researchers utilize this compound in chromatography and mass spectrometry for the separation and identification of complex mixtures, enhancing the accuracy of analytical methods.

Citations