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47626

Sigma-Aldrich

Fmoc-Gln-OH

≥95.0% (T)

Synonym(s):

Fmoc-L-glutamine

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About This Item

Empirical Formula (Hill Notation):
C20H20N2O5
CAS Number:
71989-20-3
Molecular Weight:
368.38
Beilstein/REAXYS Number:
4722773
EC Number:
276-254-3
MDL number:
MFCD00037137
UNSPSC Code:
12352200
PubChem Substance ID:
57651046
NACRES:
NA.26

assay

≥95.0% (T)

optical activity

[α]20/D −18.5±1.5°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

220 °C (dec.) (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

NC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C20H20N2O5/c21-18(23)10-9-17(19(24)25)22-20(26)27-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16-17H,9-11H2,(H2,21,23)(H,22,26)(H,24,25)/t17-/m0/s1

InChI key

IZKGGDFLLNVXNZ-KRWDZBQOSA-N

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Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCBP0451V
BCBF7579V
BCBD5647V
BCBB2222
456754/1

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C R Wu et al.
International journal of peptide and protein research, 31(1), 47-57 (1988-01-01)
The synthesis of a 37-peptide fragment derived from the carboxyl terminal of the beta-subunit of baboon chorionic gonadotropin has been accomplished by the continuous flow Fmoc-polyamide solid phase method. The use of N alpha-fluorenylmethoxy-carbonyl-glutamine with its sidechain protected by the
Roxana Y P Alta et al.
PloS one, 12(2), e0171729-e0171729 (2017-02-09)
Desferrioxamine (DFO) is a bacterial siderophore with a high affinity for iron, but low cell penetration. As part of our ongoing project focused on DFO-conjugates, we synthesized, purified, characterized and studied new mtDFOs (DFO conjugated to the Mitochondria Penetrating Peptides

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