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Fmoc-Lys(N3)-OH - 250 mg

Fmoc-Lys(N3)-OH - 250 mg

Item no.	AS-53100-F025
Manufacturer	AnaSpec
CASRN	159610-89-6
Amount	250 mg
Category	Peptides & Proteins Amino Acids
Type	Amino Acids
Specific against	other
Conjugate/Tag	Unconjugated
Purity	Peak Area by HPLC ≥95%
Citations	1. Vallee, M. R. J.; Majkut, P.; Wilkening, C. W.; Muller, G.; Hackenberger, C. P. R. Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins.Org. Lett. 2011 (13) 5440-5443. 2. Staudinger, H.; Meyer, J. UberneueorganischePhosphorverbindungen III. Phosphinmethylenederivative und Phosphinimine. Helvetica Chim. Acta. 1919 (2) 635-646.
ECLASS 10.1	32160406
ECLASS 11.0	32160406
UNSPSC	12352209
Alias	159610-89-6
Similar products	159610-89-6
Shipping Condition	Room temperature
Available
Manufacturer - Type	Unusual Amino Acids
Manufacturer - Category	Reagents for peptide synthesis
Shipping Temperature	RT
Storage Conditions	4 °C
Molecular Weight	394.4
Description	An unusual amino acid used in Solid Phase Peptide Synthesis (SPPS) for the synthesis of side-chain modified peptides and proteins.1 The side-chain azido (N3) group is stable in trifluoroacetic acid (TFA) or piperidine (Pip), two reagents commonly used in SPPS. The azido group can be readily converted to an amine on the solid phase or in solution via the Staudinger reduction.2
Product Group	RE1C1C
GTIN	5400535018399
Usage	Research use

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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AS-53100-F025-safety-datasheet.pdf