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Catalog Number:
04453
CAS Number:
146645-63-8
Nin-Boc-L-tryptophan
Purity:
≥ 99% (HPLC)
Synonym(s):
L-Trp(Boc)-OH
Documents
$22.03 /1G
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Product Information

Nin-Boc-L-tryptophan is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an excellent choice for researchers working on complex peptide sequences. Its unique structure allows for selective reactions, facilitating the incorporation of tryptophan into peptides while maintaining the integrity of the indole side chain.

In the pharmaceutical industry, Nin-Boc-L-tryptophan is particularly relevant for developing bioactive peptides and drug candidates that target various biological pathways. Its applications extend to the synthesis of neurotransmitter analogs and in studies related to serotonin metabolism, showcasing its importance in neuropharmacology. Researchers appreciate its ease of use in solid-phase peptide synthesis, where it can significantly streamline the production of high-purity peptides. With its robust profile and versatility, Nin-Boc-L-tryptophan stands out as a crucial building block for advancing peptide-based therapeutics.

Synonyms
L-Trp(Boc)-OH
CAS Number
146645-63-8
Purity
≥ 99% (HPLC)
Molecular Formula
C16H20N2O4
Molecular Weight
304.4
MDL Number
MFCD00237294
PubChem ID
14802674
Melting Point
248-254 °C
Appearance
White to off white powder
Conditions
Store at 0-8°C
General Information
Synonyms
L-Trp(Boc)-OH
CAS Number
146645-63-8
Purity
≥ 99% (HPLC)
Molecular Formula
C16H20N2O4
Molecular Weight
304.4
MDL Number
MFCD00237294
PubChem ID
14802674
Melting Point
248-254 °C
Appearance
White to off white powder
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

Nin-Boc-L-tryptophan is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create biologically active compounds.
  • Drug Development: It is used in the development of new drugs targeting neurological disorders, leveraging its tryptophan structure to influence serotonin pathways.
  • Bioconjugation: Researchers employ Nin-Boc-L-tryptophan in bioconjugation processes, attaching it to various biomolecules to enhance their therapeutic properties.
  • Protein Engineering: This chemical is valuable in protein engineering, allowing scientists to modify proteins for improved stability and function in therapeutic applications.
  • Research on Tryptophan Metabolism: It aids in studies exploring tryptophan metabolism and its implications in mental health, providing insights into dietary impacts on mood and behavior.

Citations