Fmoc-Lys(Boc)-OH

ALDRICH/47624 - ≥98.0% (HPLC)

Synonym: N_α-Fmoc-N_ε-Boc-L-lysine

CAS Number: 71989-26-9
Empirical Formula (Hill Notation): C₂₆H₃₂N₂O₆
Molecular Weight: 468.54
EC Number: 276-256-4
MDL Number: MFCD00037138
Linear Formula: C₂₆H₃₂N₂O₆
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-47624-1G-F	1 g	$31.30 1/EA		Add To Favorites
45-47624-10G-F	10 g	$72.70 1/EA		Add To Favorites
45-47624-25G-F	25 g	$119.00 1/EA		Add To Favorites
45-47624-100G-F	100 g	$207.00 1/EA		Add To Favorites
45-47624-1KG-F	1 kg	$1620.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

application(s)	peptide synthesis
assay	≥98.0% (HPLC)
form	solid
functional group	Boc
	Fmoc
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
optical activity	[α]20/D −12±1°, c = 1% in DMF
Quality Level	100
reaction suitability	reaction type: Fmoc solid-phase peptide synthesis
SMILES string	CC(C)(C)OC(=O)NCCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
storage temp.	2-8°C

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.
General description:	Fmoc-Lys(Boc)-OH is an amino acid derivative used as a reagent in Fmoc solid-phase peptide synthesis.
Packaging:	1, 10, 25 g in glass bottle

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	≥98.0% (HPLC)
Storage Temp.	2-8°C
UNSPSC	12352209

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