Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
00777
CAS Number:
19746-37-3
Boc -S -acetamidometil-L-cisteína
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Cys(Acm)-OH, ( R -3-(Acetilamino-metilsulfanil)-2- terc -butoxicarbonilamino-ácido propiónico
Documents
$29.34 /5G
Tamaño
Request Bulk Quote
Product Information

Boc-S-acetamidomethyl-L-cysteine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound is particularly valued in the pharmaceutical and biotechnology industries for its ability to introduce thiol groups into peptides, facilitating the formation of disulfide bonds which are essential for the stability and functionality of many biologically active molecules. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for researchers looking to streamline their synthesis processes.

In addition to its utility in peptide chemistry, Boc-S-acetamidomethyl-L-cysteine is also employed in the development of targeted drug delivery systems and in the synthesis of novel therapeutics. Its ability to form stable conjugates with various biomolecules enhances its relevance in drug design and development. Researchers and industry professionals can leverage this compound to improve the efficacy and specificity of their therapeutic agents, making it a valuable addition to any laboratory focused on innovative drug development.

Synonyms
Boc-L-Cys(Acm)-OH, ( R -3-(Acetilamino-metilsulfanil)-2- terc -butoxicarbonilamino-ácido propiónico
CAS Number
19746-37-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H20N2O5S
Molecular Weight
292.3
MDL Number
MFCD00038252
PubChem ID
4101782
Melting Point
103-117? C
Appearance
Polvo blanco
Optical Rotation
-29º ± 2º (c=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Cys(Acm)-OH, ( R -3-(Acetilamino-metilsulfanil)-2- terc -butoxicarbonilamino-ácido propiónico
CAS Number
19746-37-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H20N2O5S
Molecular Weight
292.3
MDL Number
MFCD00038252
PubChem ID
4101782
Melting Point
103-117? C
Appearance
Polvo blanco
Optical Rotation
-29º ± 2º (c=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-S-acetamidomethyl-L-cysteine 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.
  • Drug Development: Its role in drug design is significant, particularly in developing compounds that target specific biological pathways. Researchers can modify its structure to enhance efficacy and reduce side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps in attaching biomolecules to drugs or imaging agents, improving the delivery and effectiveness of therapeutic agents.
  • Antioxidant Research: It has applications in studying antioxidant properties, which are vital for developing treatments for conditions related to oxidative stress, such as neurodegenerative diseases.
  • Protein Engineering: This chemical is instrumental in protein engineering, where it aids in the design of proteins with enhanced stability and functionality, benefiting industries like biotechnology and pharmaceuticals.

Citas