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Alkyne Modifier I, NHS ester [PEG1 alkyne NHS ester]

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Physical properties
Molecular weight225.20
SolventDMF
Storage, safety and handling
Intended useResearch Use Only (RUO)
StorageFreeze (< -15 °C); Minimize light exposure

OverviewpdfSDSpdfProtocol


CAS
1174157-65-3
Molecular weight
225.20
Alkyne Modifier I, NHS ester (propargyl-NHS ester) is an alkyne-containing reagent that reacts with primary amines at pH 7-9 forming a stale amide bond. The terminal alkyne group reacts with azides by a mechanism known as the Cu-catalyzed click reaction enabling efficient and specific conjugation of derivatized molecules in biological samples. A short spacer arm adds minimal mass to modified molecules. It is widely used to introduce an alkynyl group into amino-modified oligonucleotides, peptides, proteins and other biological molecules.

Calculators


Common stock solution preparation

Table 1. Volume of DMF needed to reconstitute specific mass of Alkyne Modifier I, NHS ester [PEG1 alkyne NHS ester] to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM444.05 µL2.22 mL4.44 mL22.202 mL44.405 mL
5 mM88.81 µL444.05 µL888.099 µL4.44 mL8.881 mL
10 mM44.405 µL222.025 µL444.05 µL2.22 mL4.44 mL

Molarity calculator

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Citations


View all 34 citations: Citation Explorer
Synthesis and Fabrication of Surface-Active Microparticles Using a Membrane Emulsion Technique and Conjugation of Model Protein via Strain-Promoted Azide-Alkyne Click Chemistry in Physiological Conditions
Authors: Walden, G., Liao, X., Riley, G., Donell, S., Raxworthy, M. J., Saeed, A.
Journal: Bioconjug Chem (2019): 531-535
Ultrasound-assisted Cu(I)-catalyzed azide-alkyne click cycloaddition as polymer-analogous transformation in chitosan chemistry. High antibacterial and transfection activity of novel triazol betaine chitosan derivatives and their nanoparticles
Authors: Kritchenkov, A. S., Egorov, A. R., Dysin, A. P., Volkova, O. V., Zabodalova, L. A., Suchkova, E. P., Kurliuk, A. V., Shakola, T. V.
Journal: Int J Biol Macromol (2019): 592-603
Injectable Catalyst-Free Poly(Propylene Fumarate) System Cross-Linked by Strain Promoted Alkyne-Azide Cycloaddition Click Chemistry for Spine Defect Filling
Authors: Liu, X., Miller, A. L., 2nd, Xu, H., Waletzki, B. E., Lu, L.
Journal: Biomacromolecules (2019): 3352-3365
Correction: CuAAC click chemistry for the enhanced detection of novel alkyne-based natural product toxins
Authors: Hems, E. S., Wagstaff, B. A., Saalbach, G., Field, R. A.
Journal: Chem Commun (Camb) (2018): 13161
Site-Specific Surface Functionalization via Microchannel Cantilever Spotting (microCS): Comparison between Azide-Alkyne and Thiol-Alkyne Click Chemistry Reactions
Authors: Dadfar, S. M. M., Sekula-Neuner, S., Bog, U., Trouillet, V., Hirtz, M.
Journal: Small (2018): e1800131
O-GlcNAcylation site mapping by (azide-alkyne) click chemistry and mass spectrometry following intensive fractionation of skeletal muscle cells proteins
Authors: Deracinois, B., Camoin, L., Lambert, M., Boyer, J. B., Dupont, E., Bastide, B., Cieniewski-Bernard, C.
Journal: J Proteomics (2018): 83-97
Ribosome-Templated Azide-Alkyne Cycloadditions Using Resistant Bacteria as Reaction Vessels: in Cellulo Click Chemistry
Authors: Jin, X., Daher, S. S., Lee, M., Buttaro, B., Andrade, R. B.
Journal: ACS Med Chem Lett (2018): 907-911
CuAAC click chemistry for the enhanced detection of novel alkyne-based natural product toxins
Authors: Hems, E. S., Wagstaff, B. A., Saalbach, G., Field, R. A.
Journal: Chem Commun (Camb) (2018): 12234-12237
Detection of Alkynes via Click Chemistry with a Brominated Coumarin Azide by Simultaneous Fluorescence and Isotopic Signatures in Mass Spectrometry
Authors: Yang, L., Chumsae, C., Kaplan, J. B., Moulton, K. R., Wang, D., Lee, D. H., Zhou, Z. S.
Journal: Bioconjug Chem (2017): 2302-2309
Synthesis of Polystyrene and Poly(4-vinylpyridine) Mixed Grafted Silica Nanoparticles via a Combination of ATRP and Cu(I) -Catalyzed Azide-Alkyne Click Chemistry
Authors: Wu, L., Glebe, U., Boker, A.
Journal: Macromol Rapid Commun (2017): se name="4531.enl" path="C:\Users\aatbi\Dropb