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Catalog Number:
06617
CAS Number:
3226-92-4
Trityl-L-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Trt-L-Phe-OH
Documents
$89.13 /5G
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Product Information

Trityl-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a trityl protecting group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure allows for selective deprotection, facilitating the synthesis of bioactive peptides that can be used in drug development and therapeutic applications.

In addition to its role in peptide synthesis, Trityl-L-phenylalanine is also valuable in the study of protein interactions and enzyme activity. Its ability to mimic natural amino acids while providing additional stability makes it a preferred choice for researchers aiming to explore protein folding and function. The compound's compatibility with various coupling reagents further enhances its utility in organic synthesis, making it a staple in both academic and industrial laboratories.

Synonyms
Trt-L-Phe-OH
CAS Number
3226-92-4
Purity
≥ 98% (HPLC)
Molecular Formula
C28H25NO2
Molecular Weight
407.81
MDL Number
MFCD01076154
PubChem ID
14283983
Melting Point
78-82 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +33 ± 2º (C=1 in acetone)
Conditions
Store at 0-8 °C
General Information
Synonyms
Trt-L-Phe-OH
CAS Number
3226-92-4
Purity
≥ 98% (HPLC)
Molecular Formula
C28H25NO2
Molecular Weight
407.81
MDL Number
MFCD01076154
PubChem ID
14283983
Melting Point
78-82 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +33 ± 2º (C=1 in acetone)
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

Trityl-L-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting the overall structure.
  • Pharmaceutical Development: It is used in the development of drug candidates, particularly in designing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Biotechnology: In the field of biotechnology, it aids in the stabilization of proteins, improving their functionality in various applications, including enzyme production and diagnostics.
  • Research in Neuroscience: Trityl-L-phenylalanine is valuable in studying neurotransmitter interactions, contributing to advancements in understanding neurological disorders.
  • Cosmetic Formulations: The compound is also explored in cosmetic formulations for its potential to enhance skin penetration of active ingredients, leading to improved product performance.

Citations