Basic information Safety Supplier Related

Biotin-PEG<sub>4</sub>-Azide

Basic information Safety Supplier Related

Biotin-PEG<sub>4</sub>-Azide Basic information

Product Name:
Biotin-PEG<sub>4</sub>-Azide
Synonyms:
  • N-(14-Azido-3,6,9,12-tetraoxatetradecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
  • (+)-Biotin-PEG4-CH2CH2N3
  • Biotin-PEG4-azide,Biotin-PEG4-N3
  • N-[2-[2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]ethoxy]ethyl]biotinamide
  • Biotin-PEG4-CH2CH2N3/1H-Thieno[3,4-d]imidazole-4-pentanamide, N-(14-azido-3,6,9,12-tetraoxatetradec-1-yl)hexahydro-2-oxo-, (3aS,4S,6aR)-
  • Biotin-PEG4-Azide
CAS:
1309649-57-7
MF:
C20H36N6O6S
MW:
488.60144
Product Categories:
  • peg
Mol File:
1309649-57-7.mol
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Biotin-PEG<sub>4</sub>-Azide Chemical Properties

Melting point:
102.0 to 106.0 °C
storage temp. 
-20°C, sealed storage, away from moisture
form 
powder to lump
color 
White to Light yellow
InChIKey
PVEHVEYAPUNCCP-LLFBLNAENA-N
SMILES
C(NCCOCCOCCOCCOCCN=[N+]=[N-])(=O)CCCC[C@H]1[C@@]2([H])NC(=O)N[C@@]2([H])CS1 |&1:24,25,31,r|
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Safety Information

HS Code 
2934.99.9001
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Biotin-PEG<sub>4</sub>-Azide Usage And Synthesis

Description

Biotin-PEG4-azide is a very useful biotinylation reagent that enable Click Chemistry reaction with alkyne, such as Propargyl, DBCO or BCN reagent to form a stable bond. PEG4 spacer increases aqueous solubility of the molecules conjugated to the biotin. It also helps to minimize steric hindrance involved with the binding to avidin molecules.

Uses

Biotin-PEG4-azide is a biotin-labeled, PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. Biotin-PEG4-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

IC 50

PEGs

References

[1] Gadd MS, et al. Structural basis of PROTAC cooperative recognition for selective protein degradation. Nat Chem Biol. 2017 May;13(5):514-521. DOI:10.1038/nchembio.2329

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