359688

Boc-Lys-OH

99%

• Synonym(e): N_α-(tert.-Butoxycarbonyl)-L-lysin, N_α-Boc-L-lysin
• Lineare Formel: NH₂(CH₂)₄CH(COOH)NHCOOC(CH₃)₃
• CAS-Nummer: 13734-28-6
• Molekulargewicht: 246.30
• Beilstein: 4252546
• MDL-Nummer: MFCD00038203
• UNSPSC-Code: 12352209
• eCl@ss: 32160406
• PubChem Substanz-ID: 24862098
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 200
• Assay: 99%
• Form: solid
• Optische Aktivität: [α]/D 4.1 to 5.1°, c = 2 in water
• Eignung der Reaktion: reaction type: Boc solid-phase peptide synthesis
• mp (Schmelzpunkt): ~205 °C (dec.) (lit.)
• Anwendung(en): 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
• InChIKey: DQUHYEDEGRNAFO-QMMMGPOBSA-N

Beschreibung

Anwendung

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.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)