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772054

Sigma-Aldrich

Fmoc-D-Lys(Boc)-OH

98%, for peptide synthesis

Synonym(s):

Nα-Fmoc-N-ε-Boc-D-lysine

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About This Item

Empirical Formula (Hill Notation):
C26H32N2O6
CAS Number:
92122-45-7
Molecular Weight:
468.54
MDL number:
MFCD00065660
UNSPSC Code:
12352209
PubChem Substance ID:
329767535
NACRES:
NA.26

product name

Fmoc-D-Lys(Boc)-OH, 98%

Quality Level

100

assay

98%

form

powder or crystals

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

128-131 °C

application(s)

peptide synthesis

functional group

Boc
Fmoc

storage temp.

2-8°C

SMILES string

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

InChI

1S/C26H32N2O6/c1-26(2,3)34-24(31)27-15-9-8-14-22(23(29)30)28-25(32)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m1/s1

InChI key

UMRUUWFGLGNQLI-JOCHJYFZSA-N

Related Categories

related product

Product No.
Description
Pricing

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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In this work, mitochondria-targeting gold nanostar (AuNS) and anticarcinogen DOX were co-encapsulated in hyaluronic acid (HA) protective shell for tumor-targeting synergistic photothermal/chemo-therapy. Cationic peptide R
Andreas Pech et al.
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Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts

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