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About This Item
Empirical Formula (Hill Notation):
C17H27F6N7OP2
CAS Number:
Molecular Weight:
521.38
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, 96%
Quality Segment
assay
96%
form
powder
reaction suitability
reaction type: Coupling Reactions
mp
163-168 °C (lit.)
application(s)
peptide synthesis
storage temp.
−20°C
SMILES string
F[P-](F)(F)(F)(F)F.C1CCN(C1)[P+](On2nnc3cccnc23)(N4CCCC4)N5CCCC5
InChI
1S/C17H27N7OP.F6P/c1-2-11-21(10-1)26(22-12-3-4-13-22,23-14-5-6-15-23)25-24-17-16(19-20-24)8-7-9-18-17;1-7(2,3,4,5)6/h7-9H,1-6,10-15H2;/q+1;-1
InChI key
CBZAHNDHLWAZQC-UHFFFAOYSA-N
Application
Reagent for synthesis of:
Cyclic RGC pentapeptides for functionalization through click chemistry
Fluorescent glucose bioprobes
ReactIR™ flow cell
Reagent for:
Disulfide bond engineering
Heteroaryl ether synthesis
Optimization of conformational constraint on non-phosphorylated cyclic peptide antagonists of the Grb2-SH2 domain
Cyclic RGC pentapeptides for functionalization through click chemistry
Fluorescent glucose bioprobes
ReactIR™ flow cell
Reagent for:
Disulfide bond engineering
Heteroaryl ether synthesis
Optimization of conformational constraint on non-phosphorylated cyclic peptide antagonists of the Grb2-SH2 domain
Legal Information
Sold under agreement with PE Biosystems
ReactIR is a trademark of Mettler-Toledo, Inc.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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