Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
15538
CAS Number:
401916-49-2
Fmoc-(R-3-amino-4-(4-tertbutylphenyl)butyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-b-HomoPhe(4-tBu)-OH
Documents
$72.31 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-(R)-3-amino-4-(4-tertbutylphenyl)butyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, characterized by the presence of a tert-butylphenyl group, enhances solubility and stability, making it an ideal choice for researchers focused on developing complex peptide sequences.

In the pharmaceutical industry, this compound is particularly valuable for its role in creating bioactive peptides that can serve as potential therapeutics. Its application extends to the synthesis of peptide-based drugs, where the Fmoc group allows for easy deprotection under mild conditions, facilitating efficient synthesis processes. Researchers appreciate its ability to improve the yield and purity of synthesized peptides, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-D-b-HomoPhe(4-tBu)-OH
CAS Number
401916-49-2
Purity
≥ 98% (HPLC)
Molecular Formula
C29H31NO4
Molecular Weight
457.57
MDL Number
MFCD03093579
Melting Point
87 - 93 ?C
Appearance
White powder
Optical Rotation
[a]25D = 18 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-b-HomoPhe(4-tBu)-OH
CAS Number
401916-49-2
Purity
≥ 98% (HPLC)
Molecular Formula
C29H31NO4
Molecular Weight
457.57
MDL Number
MFCD03093579
Melting Point
87 - 93 ?C
Appearance
White powder
Optical Rotation
[a]25D = 18 ± 2 º (C=1 in DMF)
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-(R)-3-amino-4-(4-tertbutylphenyl)butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide structures efficiently.
  • Drug Development: It plays a crucial role in developing pharmaceuticals, especially in designing peptide-based drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and targeting of drugs in various medical applications.
  • Research in Neuroscience: Its unique structure makes it valuable in neuroscience research, particularly in studying neuropeptides and their roles in brain function and behavior.
  • Material Science: The compound is also explored in material science for developing functional materials that can respond to biological stimuli, paving the way for innovative applications in biosensors and drug delivery systems.

Citations