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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 product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW4857
MKCT0485
MKCN0291
MKCC9898
MKBN7922V

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Nicholas J Kenyon et al.
PloS one, 8(10), e77730-e77730 (2013-11-10)
Nanocarriers can deliver a wide variety of drugs, target them to sites of interest, and protect them from degradation and inactivation by the body. They have the capacity to improve drug action and decrease undesirable systemic effects. We have previously
Jingfang Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(54), 13510-13517 (2017-07-12)
A series of cationic peptides with alternating hydrophilic and hydrophobic residues were elaborately designed and synthesized. These kinds of short peptides with protonated lysine groups can interact with anionic polyoxometalate nanoclusters through multivalent ionic bonds and hydrogen bonds, resulting in
Si Chen et al.
Biomaterials, 117, 92-104 (2016-12-13)
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.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
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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