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Catalog Number:
07991
CAS Number:
6319-96-6
ClAc-Gly-OH
Purity:
≥ 99 % (CCM)
Synonym(s):
Chloracétylglycine, Acide (2-chloro-acétylamino)-acétique
Documents
$58.39 /5G
Taille
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Informations sur le produit

ClAc-Gly-OH, also known as 2-[(2-chloroacetyl)amino]acetic acid, is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This compound features a chloroacetyl group that enhances its reactivity, making it an excellent choice for peptide synthesis and modification. Researchers often employ ClAc-Gly-OH as a building block in the development of peptide-based drugs, where its unique functional groups facilitate the introduction of various amino acids, thereby tailoring the properties of the resulting peptides for specific therapeutic targets.

In addition to its role in peptide synthesis, ClAc-Gly-OH has shown potential in the field of drug delivery systems, where it can be used to create conjugates that improve the solubility and bioavailability of poorly soluble drugs. Its ability to form stable linkages with other biomolecules makes it a valuable tool for developing targeted therapies. With its diverse applications and ability to enhance drug efficacy, ClAc-Gly-OH stands out as a crucial compound for researchers and industry professionals focused on innovative therapeutic solutions.

Numéro CAS 
6319-96-6
Formule moléculaire
C4H6ClNO3
Poids moléculaire 
151.55
Point de fusion 
105 - 109 ºC
Informations générales
Numéro CAS 
6319-96-6
Formule moléculaire
C4H6ClNO3
Poids moléculaire 
151.55
Point de fusion 
105 - 109 ºC
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

ClAc-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, which are essential for developing new drugs and therapies.
  • Bioconjugation: It is used in bioconjugation processes to link biomolecules, enhancing the efficacy of targeted drug delivery systems in cancer treatment.
  • Research in Neurobiology: ClAc-Gly-OH is applied in studies related to neurotransmitter functions, aiding in the understanding of neurological disorders.
  • Diagnostic Reagents: This chemical acts as a reagent in various diagnostic tests, improving the accuracy of biochemical assays.
  • Antibody Labeling: It is utilized for labeling antibodies in immunoassays, facilitating better detection and quantification of proteins in research.

Citations