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Catalog Number:
05365
CAS Number:
112803-72-2
Chlorhydrate d'amide de N ε -Boc-L-lysine
Purity:
≥ 99,7 % (pureté chirale)
Synonym(s):
L-Lys(Boc)-NH2·HCl
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$89.13 /1G
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Product Information

Ne-Boc-L-lysine amide hydrochloride is a versatile compound widely utilized in the fields of biochemistry and pharmaceutical research. This protected form of lysine is particularly valuable for peptide synthesis, enabling researchers to incorporate lysine residues into peptides without compromising their reactivity. Its tert-butoxycarbonyl (Boc) protective group allows for selective deprotection under mild conditions, making it an ideal choice for synthesizing complex biomolecules. Additionally, the hydrochloride salt form enhances its solubility in aqueous solutions, facilitating its use in various biological assays and formulations.

This compound is especially relevant for researchers focusing on drug development and protein engineering, as it can be used to create modified peptides with enhanced stability and bioactivity. Its unique properties make it a preferred choice for applications in medicinal chemistry, where precise modifications of amino acids are crucial for optimizing therapeutic efficacy. Ne-Boc-L-lysine amide hydrochloride stands out for its ability to streamline peptide synthesis while maintaining the integrity of the target molecules, making it an essential tool for professionals in the life sciences.

Synonyms
L-Lys(Boc)-NH2·HCl
CAS Number
112803-72-2
Purity
≥ 99,7 % (pureté chirale)
Molecular Formula
C11H23N3O3 · HCl
Molecular Weight
281.8
MDL Number
MFCD00153446
PubChem ID
76420119
Melting Point
180 - 195 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 25 D = 16,5 ± 1,5 ° (C = 1 dans AcOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
L-Lys(Boc)-NH2·HCl
CAS Number
112803-72-2
Purity
≥ 99,7 % (pureté chirale)
Molecular Formula
C11H23N3O3 · HCl
Molecular Weight
281.8
MDL Number
MFCD00153446
PubChem ID
76420119
Melting Point
180 - 195 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 25 D = 16,5 ± 1,5 ° (C = 1 dans AcOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ne-Boc-L-lysine amide hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, especially in the development of therapeutic proteins and biologics.
  • Drug Development: It plays a significant role in pharmaceutical research, particularly in creating drug candidates that target specific biological pathways.
  • Bioconjugation: Researchers use it for bioconjugation processes, linking biomolecules to enhance drug delivery systems or create targeted therapies.
  • Protein Engineering: The compound is essential in modifying proteins to improve their stability and efficacy, which is crucial in the development of vaccines and enzyme therapies.
  • Research in Immunology: It is applied in the study of immune responses, aiding in the design of immunotherapeutic agents that can effectively target diseases.

Citations