Skip to Content
Merck
CN
All Photos(4)

Documents

760765

Sigma-Aldrich

Azide-fluor 488

≥90% (HPLC)

Synonym(s):

Rhodamine 110-azide

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

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

Quality Level

100

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Chemical tools for studying the biological function of glycolipids.
Stocker BL & Timmer MS
Chembiochem, 14(10), 1164-1184 (2013)
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)
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)
Drawing in poly (e-caprolactone) fibers: tuning mechanics, fiber dimensions and surface-modification density
Kim SE, et al.
Journal of Material Chemistry B: Materials for Biology and Medicine (2017)
View All Related Papers

Articles

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service