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760765

Sigma-Aldrich

Azide-fluor 488

≥90% (HPLC)

Synonym(s):

Rhodamine 110-azide

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About This Item

Empirical Formula (Hill Notation):
C29H30N6O7
Molecular Weight:
574.58
UNSPSC Code:
12352125
NACRES:
NA.22

Assay

≥90% (HPLC)

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

Related Categories

Application

Rhodamine 110 conjugated PEG azide. Can be used to detect or label alkyne- or cyclooctyne-containing molecules or biomolecules by fluorescence spectroscopy following azide-alkyne cycloaddition.

Spectral Properties: Abs/Em = 501/525 nm

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Two-step local functionalization of fluoropolymer Dyneon THV microfluidic materials by scanning electrochemical microscopy combined to click reaction.
Slim C, et al.
Electrochemical Communications, 60, 5-8 (2015)
Chemical tools for studying the biological function of glycolipids.
Stocker BL & Timmer MS
Chembiochem, 14(10), 1164-1184 (2013)
Synthesis and Conjugation of Alkyne-Functional Hyperbranched Polyglycerols.
Moore E, et al.
Macromolecular Chemistry and Physics, 217(20), 2252-2261 (2016)
Indole-induced Reversion of Intrinsic Multi-antibiotic Resistance in Lysobacter enzymogenes.
Han Y, et al.
Applied and Environmental Microbiology, AEM-00995 (2017)
Matrix metalloproteinase responsive delivery of myostatin inhibitors.
Braun AC, et al.
Pharmaceutical Research, 34(1), 58-72 (2017)
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Click Chemistry in Drug Discovery

Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.

Click Chemistry in Drug Discovery

Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.

Click Chemistry in Drug Discovery

Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.

Click Chemistry in Drug Discovery

Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.

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