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Catalog Number:
36592
CAS Number:
18342-66-0
N- Succinimidyl N -méthylcarbamate
Purity:
≥ 97 % (analyse élémentaire)
Synonym(s):
Substitut de l'isocyanate de méthyle
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Product Information

N-Succinimidyl N-methylcarbamate is a versatile chemical compound widely utilized in bioconjugation and drug delivery applications. This compound serves as an effective crosslinker and labeling agent, particularly in the development of targeted therapeutics and diagnostic tools. Its unique structure allows for the formation of stable conjugates with proteins, peptides, and other biomolecules, enhancing their stability and functionality. Researchers appreciate its ability to facilitate the attachment of various functional groups, making it an essential tool in the fields of proteomics and molecular biology.

In addition to its role in bioconjugation, N-Succinimidyl N-methylcarbamate is also employed in the synthesis of novel pharmaceuticals, where it aids in the design of prodrugs that improve bioavailability and therapeutic efficacy. Its ease of use and compatibility with a range of biological systems make it a preferred choice for scientists and industry professionals looking to innovate in drug development and biomolecular research. With its proven effectiveness and broad applicability, N-Succinimidyl N-methylcarbamate stands out as a valuable asset in the chemical toolkit for advancing scientific discovery.

Synonyms
Substitut de l'isocyanate de méthyle
CAS Number
18342-66-0
Purity
≥ 97 % (analyse élémentaire)
Molecular Formula
C6H8N2O4
Molecular Weight
172.14
MDL Number
MFCD00800292
PubChem ID
4381935
Appearance
Solide blanc à blanc cassé
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
General Information
Synonyms
Substitut de l'isocyanate de méthyle
CAS Number
18342-66-0
Purity
≥ 97 % (analyse élémentaire)
Molecular Formula
C6H8N2O4
Molecular Weight
172.14
MDL Number
MFCD00800292
PubChem ID
4381935
Appearance
Solide blanc à blanc cassé
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Succinimidyl N-methylcarbamate is widely utilized in research focused on:

  • Bioconjugation: This compound is often used to attach biomolecules, such as proteins and antibodies, to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Protein Labeling: It serves as a reagent for labeling proteins in various assays, allowing researchers to track and study protein interactions and functions effectively.
  • Drug Development: In pharmaceutical research, it is employed to create prodrugs, which can improve the solubility and bioavailability of therapeutic compounds.
  • Diagnostic Applications: The compound is used in the development of diagnostic tools, such as enzyme-linked immunosorbent assays (ELISA), facilitating the detection of specific biomolecules.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding in the development of potential treatments for neurological disorders.

Citations