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47624

Fmoc-Lys(Boc)-OH

Name: Fmoc-Lys(Boc)-OH
Brand: ALDRICH

≥98.0% (HPLC), for peptide synthesis

Synonym(s):

N_α-Fmoc-N_ε-Boc-L-lysine

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About This Item

Empirical Formula (Hill Notation):

C₂₆H₃₂N₂O₆

CAS Number:

71989-26-9

Molecular Weight:

468.54

NACRES:

NA.26

PubChem Substance ID:

57651044

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

276-256-4

MDL number:

MFCD00037138

Beilstein/REAXYS Number:

4217767

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Properties

Product Name

Fmoc-Lys(Boc)-OH, ≥98.0% (HPLC)

Quality Segment

100

assay

≥98.0% (HPLC)

form

solid

optical activity

[α]20/D −12±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

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-/m0/s1

InChI key

UMRUUWFGLGNQLI-QFIPXVFZSA-N

Description

General description

Fmoc-Lys(Boc)-OH is an amino acid derivative used as a reagent in Fmoc solid-phase peptide synthesis.

Application

Fmoc-Lys(Boc)-OH can be used for:

The solid-phase synthesis of pentasubstituted dihydroimidazolylbutyl dihydroimidazol-3-ium salts by coupling with p-methylbenzhydrylamine (MBHA) resin.
Fmoc-based peptide synthesis of bis-naphthalene diimide, a threading intercalator.
Synthesis of ε-Boc-ε-(3,5-bis-trifluoromethyl-benzyl)-α-Fmoc-L-Lysine to be used as ¹⁹F NMR based screening tool.

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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