8.52135
Fmoc-Asn(Ac₃AcNH-ß-Glc)-OH
≥95.0% (HPLC), for peptide synthesis, Novabiochem®
Synonym(s):
Fmoc-Asn(Ac₃AcNH-ß-Glc)-OH, N-α-Fmoc-N-β-[3,4,6-tri-O-acetyl-2-(acetylamino)-deoxy-2-β-glucopyranosyl]-L-asparagine
About This Item
Recommended Products
product name
Fmoc-Asn(Ac₃AcNH-ß-Glc)-OH, Novabiochem®
Quality Level
product line
Novabiochem®
Assay
≥95% (TLC)
≥95.0% (HPLC)
form
powder
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
manufacturer/tradename
Novabiochem®
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
15-25°C
InChI
1S/C33H37N3O13/c1-16(37)34-28-30(48-19(4)40)29(47-18(3)39)26(15-45-17(2)38)49-31(28)36-27(41)13-25(32(42)43)35-33(44)46-14-24-22-11-7-5-9-20(22)21-10-6-8-12-23(21)24/h5-12,24-26,28-31H,13-15H2,1-4H3,(H,34,37)(H,35,44)(H,36,41)(H,42,43)/t25-,26+,28+,29+,30+,31+/m0/s1
InChI key
QOACISSHGAAMLK-MJCYOTSPSA-N
Related Categories
General description
Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Fmoc SPPS of Peptides containing Post-Translational Modifications
Literature references
[1] L. Otvos, et al. (1989) Pept. Res., 2, 362.
[2] M. Meldal, et al. (1990) Tetrahedron Lett., 31, 6987.
[3] L. Otvos, et al. (1990) Tetrahedron Lett., 31, 5889.
[4] J. Price, et al. (2010) J. Am. Chem. Soc., 132, 15359.
Linkage
Analysis Note
Appearance of substance (visual): powder
Identity (IR): passes test
Purity (TLC(CMA2)): ≥ 95 %
Assay (HPLC, area%): ≥ 95.0 % (a/a)
Identity (NMR, 1H): passes test
Identity (NMR): passes test
NMR-spectrum: passes test
To see the solvent systems used for TLC of Novabiochem® products please click here.
Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Protocols
We provide an overview of our available reagents, together with recommendations and details of their use for synthesis of peptides containing post-translationally modified amino acids.
We provide an overview of our available reagents, together with recommendations and details of their use for synthesis of peptides containing post-translationally modified amino acids.
We provide an overview of our available reagents, together with recommendations and details of their use for synthesis of peptides containing post-translationally modified amino acids.
We provide an overview of our available reagents, together with recommendations and details of their use for synthesis of peptides containing post-translationally modified amino acids.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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