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A propos de cet article
Formule empirique (notation de Hill) :
C11H16F6N5OP
Numéro CAS:
Poids moléculaire :
379.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352107
EC Number:
423-020-5
MDL number:
Beilstein/REAXYS Number:
7328329
Service technique
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Laissez-nous vous aiderNom du produit
HBTU, ≥98.0% (T)
Quality Level
assay
≥98.0% (T)
form
solid
reaction suitability
reaction type: Coupling Reactions
mp
200 °C (dec.) (lit.)
solubility
acetonitrile: 0.1 g/mL, clear
application(s)
peptide synthesis
functional group
amine
storage temp.
2-8°C
SMILES string
F[P-](F)(F)(F)(F)F.CN(C)C(\On1nnc2ccccc12)=[N+](/C)C
InChI
1S/C11H16N5O.F6P/c1-14(2)11(15(3)4)17-16-10-8-6-5-7-9(10)12-13-16;1-7(2,3,4,5)6/h5-8H,1-4H3;/q+1;-1
InChI key
UQYZFNUUOSSNKT-UHFFFAOYSA-N
General description
HBTU is a peptide coupling agent used in Fmoc-based solid-phase peptide synthesis.
Application
Recent studies show that crystal as well as solution structure of this coupling agent is a guanidinium N-oxide and not an uronium compound; Coupling reagent for peptide synthesis; advantages are: very low racemization, simple reaction conditions, very short reaction time, and high yields.
HBTU is a peptide coupling agent for peptide synthesis. It has also been used in standard Fmoc-based solid-phase peptide synthesis (SPPS) protocol.
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1A
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Structural studies of reagents for peptide bond formation: Crystal and molecular structures of HBTU and HATU.
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