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boc-lys-oh (c15-1213-507)

N-ALPHA-(TERT-BUTOXYCARBONYL)-L-LYSINE 99% (C005B-016441)

Catalog No.
C005B-016441
Manufacturer No.
359688-1G
Manufacturer Name
Sigma-Aldrich
Quantity
1
Unit of Measure
GR

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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.

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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.

Molecular Weight: 246.30. Empirical Formula: C11H22N2O4. linearFormula: NH2(CH2)4CH(COOH)NHCOOC(CH3)3. 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. Storage Class Code: 11 - Combustible Solids. WGK: WGK 3. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).
UPC:
12141907
Condition:
New
HazmatClass:
No
MPN:
359688-1G
CAS:
13734-28-6

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