15456

Boc-Lys-OH

≥99.0% (NT)

• 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
• EC Number: 237-303-4
• MDL number: MFCD00038203
• UNSPSC Code: 12352209
• eCl@ss: 32160406
• PubChem Substance ID: 57647439
• NACRES: NA.22

Properties

• Quality Level: 200
• assay: ≥99.0% (NT)
• form: solid
• optical activity: [α]20/D +4.6±0.5°, c = 2% in H₂O
• 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

General description

Boc-Lys-OH also known as Nα-Boc-L-lysine, is an amino acid derivative of lysine which is used in solid phase peptide synthesis.

Application

Boc-Lys-OH is used as a building block to form peptides that have bioorthogonal reactive groups via boc protected solid phase synthesis.

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)