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Fmoc-β-azido-Ala-OH

ALDRICH/714151 - ≥98.0% (HPLC)

Synonym: (S)-3-Azido-2-(Fmoc-amino)propionic acid; Fmoc-3-azido-L-alanine

CAS Number: 684270-46-0
Empirical Formula (Hill Notation): C18H16N4O4
Molecular Weight: 352.34
MDL Number: MFCD11052919
Linear Formula: C18H16N4O4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-714151-250MG 250 mg
 $456.00
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application(s) peptide synthesis
assay ≥98.0% (HPLC)
form lumps
functional group Fmoc
impurities 15.3-16.5% nitrogen
  60.1-62.5% carbon
InChI 1S/C18H16N4O4/c19-22-20-9-16(17(23)24)21-18(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H,21,25)(H,23,24)/t16-/m0/s1
InChI key ZITYCUDVCWLHPG-INIZCTEOSA-N
optical activity [α]/D -10.0±1.0°, c = 1 in DMF
Quality Level 100 
reaction suitability reaction type: click chemistry
  reaction type: Fmoc solid-phase peptide synthesis
SMILES string OC(=O)[C@H](CN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c3ccccc13
storage temp. 2-8°C
Application: Fmoc-β-azido-Ala-OH chloride is a general N-terminal protected reagent used in the solid phase peptide synthesis. Azido group allows it to undergo copper-mediated click chemistry reactions.
It can be used in:
• Synthesis of α-N-acetylgalactosamine (α-GalNAc) linked antifreeze glycopeptides (AFGPs).
• Synthesis of stimuli-responsive multifunctional peptide gatekeepers for drug delivery applications.
• Synthesis of triazole-linked glycopeptides via Cu(I)-catalyzed 1,3-dipolar cycloaddition (CuAAC).
Packaging: 250 mg in glass bottle
Packaging: Bottomless glass bottle. Contents are inside inserted fused cone.
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98.0% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352209

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