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8.52123

Sigma-Aldrich

Fmoc-Glu(OAll)-OH

Novabiochem®

Synonym(s):

Fmoc-Glu(OAll)-OH

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About This Item

Empirical Formula (Hill Notation):
C23H23NO6
CAS Number:
Molecular Weight:
409.43
MDL number:
UNSPSC Code:
12352209
NACRES:
NA.22

Quality Level

product line

Novabiochem®

assay

≥97.0% (HPLC)
≥97.0% (acidimetric)
≥98% (TLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

manufacturer/tradename

Novabiochem®

application(s)

peptide synthesis

functional group

carboxylic acid

storage temp.

2-30°C

InChI

1S/C23H23NO6/c1-2-13-29-21(25)12-11-20(22(26)27)24-23(28)30-14-19-17-9-5-3-7-15(17)16-8-4-6-10-18(16)19/h2-10,19-20H,1,11-14H2,(H,24,28)(H,26,27)/t20-/m0/s1

InChI key

LRBARFFNYOKIAX-FQEVSTJZSA-N

General description

Orthogonally-protected building block for the synthesis of peptides modified at the Glu side chain by Fmoc SPPS. See entry for 852073 for more details.

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Guide to Selection of Orthogonally -Protected Building Blocks for Fmoc SPPS

Linkage

Replaces: 04-12-1304

Analysis Note

Color (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Optical rotation α 25/D (c=1 in DMF): -19.0 - -16.0 °
Purity (TLC(157A)): ≥ 98 %
Assay (HPLC, area%): ≥ 97.0 % (a/a)
Solubility (1 mmole in 2 ml DMF): clearly soluble
Assay (acidimetric): ≥ 97.0 %
Water (K. F.): ≤ 1.0 %
Identity (LC-MS): 408.4 - 410.4

To see the solvent systems used for TLC of Novabiochem® products please click here.

Legal Information

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

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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Articles

Novabiochem® offers orthogonally protected amino acids for peptide synthesis, including cyclic and branched peptides.

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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