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Catalog Number:
16855
CAS Number:
158149-99-6
L-2-Aminomethylphenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
L-Phe(2-CH2NH2)-OH, (2S-2-Amino-3-[2-(aminomethyl)phenyl]propanoic acid, H-Phe(2-CH2NH2)-OH
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Product Information

L-2-Aminomethylphenylalanine is a versatile amino acid derivative that plays a significant role in various biochemical applications. This compound, also known as 2-Aminomethyl-phenylalanine, is particularly valued in the fields of pharmaceuticals and biotechnology. Its unique structure allows it to serve as a building block in the synthesis of peptide-based drugs and as a precursor in the development of novel therapeutic agents. Researchers have utilized L-2-Aminomethylphenylalanine in studies focused on neuropharmacology, where it has shown potential in modulating neurotransmitter activity, thereby influencing cognitive functions and mood regulation.

In addition to its applications in drug development, L-2-Aminomethylphenylalanine is also explored for its potential in the synthesis of advanced materials and bioconjugates. Its ability to form stable bonds with various biomolecules makes it an attractive candidate for creating targeted delivery systems in drug formulation. With its growing relevance in research and industry, L-2-Aminomethylphenylalanine stands out as a compound with promising applications that can enhance the efficacy of therapeutic interventions and materials science.

Synonyms
L-Phe(2-CH2NH2)-OH, (2S-2-Amino-3-[2-(aminomethyl)phenyl]propanoic acid, H-Phe(2-CH2NH2)-OH
CAS Number
158149-99-6
Purity
≥ 99% (HPLC)
Molecular Formula
C10H14N2O2
Molecular Weight
194.23
MDL Number
MFCD06659114
PubChem ID
22174430
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +5.5 ± 0.5º (C=1 in 1N HCl)
Conditions
Store at 0-8°C
General Information
Synonyms
L-Phe(2-CH2NH2)-OH, (2S-2-Amino-3-[2-(aminomethyl)phenyl]propanoic acid, H-Phe(2-CH2NH2)-OH
CAS Number
158149-99-6
Purity
≥ 99% (HPLC)
Molecular Formula
C10H14N2O2
Molecular Weight
194.23
MDL Number
MFCD06659114
PubChem ID
22174430
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +5.5 ± 0.5º (C=1 in 1N HCl)
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

L-2-Aminomethylphenylalanine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in the creation of peptides, which are essential in biochemistry and molecular biology for studying protein interactions and functions.
  • Biochemical Research: Researchers leverage its unique properties to explore enzyme activity and protein folding, contributing to advancements in understanding cellular processes.
  • Drug Design: The compound plays a key role in structure-activity relationship studies, helping scientists design more effective and selective therapeutic agents.
  • Cosmetic Formulations: It is also being explored in the cosmetic industry for its potential benefits in skin care products, particularly those targeting anti-aging and skin repair.

Citations