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760757

Sigma-Aldrich

Azide-fluor 545

Synonym(s):

5-Carboxytetramethylrhodamine-azide, TAMRA PEG azide., TAMRA-azide, Tetramethylrhodamine

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About This Item

Empirical Formula (Hill Notation):
C33H39N6O7
Molecular Weight:
631.70
UNSPSC Code:
12171501
NACRES:
NA.22

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

Related Categories

Application

Azide-fluor 545 can be used to label alkyne/cyclooctyne containing molecules or biomolecules by azide-alkyne click chemistry.
Can be used to detect or label alkyne- or cyclooctyne-containing molecules or biomolecules by fluorescence spectroscopy following an azide-alkyne click chemistry reaction.

Spectral Properties: Abs/Em = 546/565 nm

related product

Product No.
Description
Pricing

924083

TAMRA-a-TCO

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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Atto 594 azide

Post isolation modification of exosomes for nanomedicine applications.
Hood JL.
Nanomedicine (London, England), 11(13), 1745-1756 (2016)
Surface functionalization of exosomes using click chemistry.
Smyth T, et al.
Bioconjugate Chemistry, 25(10), 1777-1784 (2014)
Genetic Encoding of a Bicyclo [6.1. 0] nonyne-Charged Amino Acid Enables Fast Cellular Protein Imaging by Metal-Free Ligation.
Borrmann A, et al.
Chembiochem, 13(14), 2094-2099 (2012)
Engineering exosomes as refined biological nanoplatforms for drug delivery.
Luan X, et al.
Acta Pharmacologica Sinica, 38(6), 754-754 (2017)
A toolbox for controlling the properties and functionalisation of hydrazone-based supramolecular hydrogels.
Poolman JM, et al.
Journal of Material Chemistry B: Materials for Biology and Medicine, 4(5), 852-858 (2016)
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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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