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Catalog Number:
02595
CAS Number:
83427-79-6
Trityl-L- homoserine
Purity:
98+%
Synonym(s):
Trt-L-HomoSer-OH, (S-Trityl-2-amino-4-hydroxybutyric acid
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Product Information

Trityl-L-homoserine is a versatile amino acid derivative that plays a significant role in biochemical research and pharmaceutical applications. This compound is recognized for its unique trityl group, which enhances its stability and solubility, making it an ideal candidate for various synthesis processes. Researchers utilize Trityl-L-homoserine in peptide synthesis, particularly in the development of novel therapeutics and bioconjugates. Its ability to act as a protecting group for amino acids allows for greater control during chemical reactions, thereby improving yields and purity of the final products.

In addition to its applications in synthetic chemistry, Trityl-L-homoserine is also explored in the field of drug development, where it can serve as a building block for biologically active compounds. Its favorable properties, such as low toxicity and high reactivity, make it an attractive option for researchers aiming to create innovative solutions in medicinal chemistry. With its broad range of applications, Trityl-L-homoserine stands out as a valuable tool for scientists and industry professionals alike.

Synonyms
Trt-L-HomoSer-OH, (S-Trityl-2-amino-4-hydroxybutyric acid
CAS Number
83427-79-6
Purity
98+%
Molecular Formula
C23H23NO3
Molecular Weight
361.44
MDL Number
MFCD00235909
Conditions
Store at 0-8°C
General Information
Synonyms
Trt-L-HomoSer-OH, (S-Trityl-2-amino-4-hydroxybutyric acid
CAS Number
83427-79-6
Purity
98+%
Molecular Formula
C23H23NO3
Molecular Weight
361.44
MDL Number
MFCD00235909
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-homoserine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial for creating complex peptides used in pharmaceuticals.
  • Biotechnology: It is employed in the development of biopharmaceuticals, particularly in the design of therapeutic proteins. Its stability and compatibility with biological systems enhance the efficacy of drug formulations.
  • Research in Neuroscience: Trityl-L-homoserine is used in studies related to neurotransmitter synthesis, providing insights into neurological functions and potential treatments for neurodegenerative diseases.
  • Analytical Chemistry: This compound is valuable in analytical methods for detecting and quantifying amino acids in various samples, aiding researchers in food safety and quality control.
  • Cosmetic Formulations: Due to its biocompatibility, it is included in cosmetic products aimed at skin hydration and repair, appealing to the growing demand for effective skincare solutions.

Citations