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Sigma-Aldrich

Nα-Fmoc-Nε-biotinyl-L-lysine

≥95.0% (HPLC)

Synonym(s):

Nα-Biotinyl-Nε-Fmoc-L-lysine, Fmoc-Lys(biotinyl)-OH

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About This Item

Empirical Formula (Hill Notation):
C31H38N4O6S
CAS Number:
146987-10-2
Molecular Weight:
594.72
MDL number:
MFCD00270741
UNSPSC Code:
12352209
eCl@ss:
34058011
PubChem Substance ID:
57652489
NACRES:
NA.26

assay

≥95.0% (HPLC)

form

powder

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

SMILES string

[H][C@@]12CS[C@H](CCCCC(=O)NCCCC[C@H](NC(=O)OCC3c4ccccc4-c5ccccc35)C(O)=O)[C@]1([H])NC(=O)N2

InChI

1S/C31H38N4O6S/c36-27(15-6-5-14-26-28-25(18-42-26)33-30(39)35-28)32-16-8-7-13-24(29(37)38)34-31(40)41-17-23-21-11-3-1-9-19(21)20-10-2-4-12-22(20)23/h1-4,9-12,23-26,28H,5-8,13-18H2,(H,32,36)(H,34,40)(H,37,38)(H2,33,35,39)/t24-,25-,26-,28-/m0/s1

InChI key

OFIBQNGDYNGUEZ-OBXRUURASA-N

Related Categories

Other Notes

Synthesis of site-specific biotinylated probes

related product

Product No.
Description
Pricing

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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M J Macielag et al.
International journal of peptide and protein research, 44(6), 582-588 (1994-12-01)
The solid-phase synthesis of two porcine motilin derivatives, specifically biotinylated on the side chain of Lys20, was accomplished by preactivation of the protected amino acids N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-biotinyl-L-lysine and N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-[N-(biotinyl)-6-aminohexanoyl]-L-lysine with BOP/HOBt/DIEA (1:1:2.5) followed by coupling to the

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