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CS-W001157 4
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Benzyl N6-(t-Boc)-L-lysinate hydrochloride

  • CAS No. 133170-57-7

  • Cat. No. CS-0129857
  • Purity≥97%
  • MDL No.MFCD11045868

*For research and further manufacturing use only, not for direct human use.

Benzyl N6-(t-Boc)-L-lysinate hydrochloride|CS-0129857

Structure of 133170-57-7

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General Information

  • CAS No. 133170-57-7
  • Cat. No. CS-0129857
  • Purity ≥97%
  • MDL No. MFCD11045868
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₂₉ClN₂O₄
  • Molecular Weight 372.89
  • Synonym(s) None
  • SMILES O=C(OCC1=CC=CC=C1)[C@@H](N)CCCCNC(OC(C)(C)C)=O.Cl

Description

Benzyl N6-(t-Boc)-L-lysinate serves as a protected lysine derivative featuring a benzyl ester and tert-butoxycarbonyl group, enabling orthogonal handling in peptide synthesis. This stable, moisture-tolerant reagent integrates seamlessly into solid-phase workflows, delivering efficient coupling with minimal racemization.

Application

Benzyl N⁶-(t-Boc)-L-lysinate serves as a versatile amino acid building block for peptide synthesis, offering orthogonal protection of the ε-amino group via the t-Boc moiety while preserving the side-chain functionality. The benzyl ester facilitates efficient deprotection under mild hydrogenolysis conditions, enabling straightforward access to free carboxylic acid derivatives. This compound exhibits excellent bench stability and compatibility with standard coupling reagents, making it ideal for iterative solid-phase and solution-phase peptide assembly workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   90.65
  • LogP   3.1739
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   8

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