914134
5-(Biotinamido)pentylamine TFA Salt
≥95%
Synonym(s):
N-(5-Aminopentyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pent, Biotin cadaverine TFA, Biotin-DAPe TFA
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About This Item
Empirical Formula (Hill Notation):
C15H28N4O2S · xC2HF3O2
Molecular Weight:
328.47 (free base basis)
MDL number:
UNSPSC Code:
12352116
NACRES:
NA.22
Pricing and availability is not currently available.
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Quality Level
Assay
≥95%
form
powder
mp
116-121 °C
storage temp.
2-8°C
SMILES string
FC(F)(F)C(=O)O.S1[C@H]([C@H]2NC(=O)N[C@H]2C1)CCCCC(=O)NCCCCCN
InChI key
QWKKJNXOPDNIEU-RGESYUBESA-N
Application
5-(Biotinamido)pentylamine TFA Salt is a versatile biotinylated linker that can be incorporated into chemical tools via its terminal amino group. Labeling materials or proteins with biotin provides a means to enrich and capture targets from biological systems.
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Automate your Biotin tagging with Synple Automated Synthesis Platform (SYNPLE-SC002)
Other Notes
Site-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffold
Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions
Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation
Synthesis of Novel Phosphonic-Type Activity-Based Probes for Neutrophil Serine Proteases and Their Application in Spleen Lysates of Different Organisms
Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions
Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation
Synthesis of Novel Phosphonic-Type Activity-Based Probes for Neutrophil Serine Proteases and Their Application in Spleen Lysates of Different Organisms
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Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Suguru Yoshida et al.
Chemical communications (Cambridge, England), 54(30), 3705-3708 (2018-03-13)
A facile strategy for the synthesis of trifunctional molecules involving three sequential selective triazole-forming reactions is proposed. This method exploits three kinds of mechanistically different azido-type-selective cycloadditions. Three different azidophiles could be efficiently connected to a triazido platform molecule with
Renata Grzywa et al.
Chembiochem : a European journal of chemical biology, 15(17), 2605-2612 (2014-09-23)
Neutrophils are a type of granulocyte important in the "first line of defense" of the innate immune system. Upon activation, they facilitate the destruction of invading microorganisms by the production of superoxide radicals, as well as the release of the
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