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Catalog Number:
04769
TentaGel S-Br (0,1 - 0,3 meq/g, billes de 130 µm)
Synonym(s):
Résine de O-(2-bromoéthyl)polyéthylène glycol
Documents
$36.65 /1G
Taille
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Product Information

Cette résine est un polystyrène faiblement réticulé et un polyéthylène glycol de poids moléculaire 3000-4000 qui a été fonctionnalisé en tant que bromure. Ce produit est idéal pour la synthèse de bibliothèques en série et en parallèle. Réf. : Rapp W. et al., Peptides 1988, Proc. 20th European Peptide Symposium, Editors Jung G. and Bayer E., Walter de Gruyter pp 199 (1989);

Synonyms
Résine de O-(2-bromoéthyl)polyéthylène glycol
Molecular Weight
0.0
MDL Number
MFCD00217898
Appearance
Poudre blanche à légèrement jaunâtre
Substitution
0,1 - 0,3 méq/g
Mesh Size
Billes de 130 µm
Conditions
Magasin chez RT
%DVB
1% DVB
General Information
Synonyms
Résine de O-(2-bromoéthyl)polyéthylène glycol
Molecular Weight
0.0
MDL Number
MFCD00217898
Appearance
Poudre blanche à légèrement jaunâtre
Substitution
0,1 - 0,3 méq/g
Mesh Size
Billes de 130 µm
Conditions
Magasin chez RT
%DVB
1% DVB
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

TentaGel S-Br (0.1 - 0.3 meq/g, 130 µm beads) is widely utilized in research focused on

  • Peptide Synthesis: This chemical is essential for solid-phase peptide synthesis, allowing researchers to create peptides efficiently with high purity and yield.
  • Drug Development: It serves as a support for high-throughput screening of drug candidates, facilitating the rapid identification of potential therapeutic compounds.
  • Bioconjugation: TentaGel S-Br is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces, which is crucial for developing biosensors and diagnostic tools.
  • Polymer Chemistry: In polymer research, it acts as a versatile scaffold for creating functionalized polymers, enhancing material properties for various applications.
  • Combinatorial Chemistry: This chemical supports combinatorial chemistry techniques, allowing for the simultaneous synthesis of multiple compounds, which accelerates the discovery process in medicinal chemistry.

Citations