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Catalog Number:
03873
CAS Number:
34078-85-8
Ester de N -hydroxysuccinimide de ZL-glutamine
Purity:
≥ 96% (Analyse élémentaire)
Synonym(s):
ZL-Gln-OSu
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Product Information

Z-L-glutamine N-hydroxysuccinimide ester is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This ester derivative of glutamine plays a crucial role in peptide synthesis and drug development, particularly in the formation of stable amide bonds. Its unique structure allows for selective coupling reactions, making it an essential tool for researchers aiming to create complex biomolecules with high specificity and efficiency.

In addition to its applications in peptide synthesis, Z-L-glutamine N-hydroxysuccinimide ester is also valuable in the field of bioconjugation, where it is used to attach biomolecules to surfaces or other molecules. This capability is particularly beneficial in the development of targeted drug delivery systems and diagnostic tools. With its high reactivity and stability, this compound stands out as a preferred choice for professionals seeking reliable and effective solutions in their research and development projects.

Synonyms
ZL-Gln-OSu
CAS Number
34078-85-8
Purity
≥ 96% (Analyse élémentaire)
Molecular Formula
C17H19N3O7
Molecular Weight
377.35
MDL Number
MFCD00153330
PubChem ID
12876460
Melting Point
125-130 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 24 = -29,6 ± 2º (C = 1 % dans EtOH)
Conditions
Conserver à ≤ -4 °C
General Information
Synonyms
ZL-Gln-OSu
CAS Number
34078-85-8
Purity
≥ 96% (Analyse élémentaire)
Molecular Formula
C17H19N3O7
Molecular Weight
377.35
MDL Number
MFCD00153330
PubChem ID
12876460
Melting Point
125-130 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 24 = -29,6 ± 2º (C = 1 % dans EtOH)
Conditions
Conserver à ≤ -4 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Z-L-glutamine N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules such as proteins or antibodies to surfaces or other molecules, enhancing the functionality of diagnostic and therapeutic agents.
  • Drug Development: In pharmaceutical research, it is used to create prodrugs that improve the solubility and bioavailability of active pharmaceutical ingredients, leading to more effective treatments with potentially fewer side effects.
  • Protein Labeling: The compound facilitates the labeling of proteins for tracking and imaging in biological studies, which is crucial for understanding protein interactions and cellular processes.
  • Peptide Synthesis: It plays a significant role in peptide synthesis, allowing for the selective modification of amino acids, which is essential for developing novel peptides with specific biological activities.
  • Diagnostics: In the field of diagnostics, it is utilized in the development of assays and sensors that detect specific biomolecules, improving the accuracy and sensitivity of medical tests.

Citations