359688

Boc-Lys-OH

99%

• Synonym(s): N_α-(tert-Butoxycarbonyl)-L-lysine, N_α-Boc-L-lysine
• Linear Formula: NH₂(CH₂)₄CH(COOH)NHCOOC(CH₃)₃
• CAS Number: 13734-28-6
• Molecular Weight: 246.30
• Beilstein/REAXYS Number: 4252546
• MDL number: MFCD00038203
• UNSPSC Code: 12352209
• eCl@ss: 32160406
• PubChem Substance ID: 24862098
• NACRES: NA.22

Properties

• Quality Level: 200
• assay: 99%
• form: solid
• optical activity: [α]20/D +22°, c = 2 in methanol
• reaction suitability: reaction type: Boc solid-phase peptide synthesis
• mp: ~205 °C (dec.) (lit.)
• application(s): peptide synthesis
• SMILES string: CC(C)(C)OC(=O)N[C@@H](CCCCN)C(O)=O
• InChI: 1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
• InChI key: DQUHYEDEGRNAFO-QMMMGPOBSA-N

Description

Application

Boc-Lys-OH (Nα-Boc-L-lysine) can be used as a building block to synthesize:

• A heterotrifunctional peptide-based linker molecule applicable as a bio-labeling reagent.
• Lysine derivatives of azamacrocycle and anthraquinone.
• Boc-Lys(Bn₄-DTPA)-OH, a precursor to synthesize diethylene triamine pentaacetic acid (DTPA) containing peptides.
• A ferrocene-amino acid conjugate which is used in developing chemical warfare agent (CWA) sensor.

Safety Information

• 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)