A building block
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Fmoc-Lys-OH (hydrochloride)

Item No. 30561

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-lysine, monohydrochloride
CAS Number
139262-23-0
Molecular Formula
C21H24N2O4 • HCl
Formula Weight
404.9
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
λmax
265 nm
SMILES
O=C(N[C@H](C(O)=O)CCCCN)OCC1C2=C(C=CC=C2)C3=C1C=CC=C3.Cl
InChi Code
InChI=1S/C21H24N2O4.ClH/c22-12-6-5-11-19(20(24)25)23-21(26)27-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18;/h1-4,7-10,18-19H,5-6,11-13,22H2,(H,23,26)(H,24,25);1H/t19-;/m0./s1
InChi Key
MVMZFAIUUXYFGY-FYZYNONXSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

Download most recent Certificate of Analysis for this product

    1 g

    $41

    Add

    5 g

    $119

    Add

    10 g

    $215

    Add
    Product Description

    Fmoc-Lys-OH is a building block.1,2 It has been used in the synthesis of azido-protected peptides for activity-based protein profiling and click-functional peptide bundles for biopolymer formation.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Katayama, H., Hojo, H., Ohira, T., et al. An efficient peptide ligation using azido-protected peptides via the thioester method. Tetrahedron Lett. 49(38), 5492-5494 (2008).

    2. Wu, D., Sinha, N., Lee, J., et al. Polymers with controlled assembly and rigidity made with click-functional peptide bundles. Nature 574(7780), 658-662 (2019).