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O-(6-Chlorobenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate

SIAL/04936 - ≥98.0% (HPLC)

Synonym: 1-[Bis(dimethylamino)methylen]-5-chlorobenzotriazolium 3-oxide hexafluorophosphate; N,N,N′,N′-Tetramethyl-O-(6-chloro-1H-benzotriazol-1-yl)uronium hexafluorophosphate; HCTU

CAS Number: 330645-87-9
Empirical Formula (Hill Notation): C11H15ClF6N5OP
Molecular Weight: 413.69
MDL Number: MFCD04973268
Linear Formula: C11H15ClF6N5OP
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-04936-5G-F 5 g
 $34.40
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45-04936-25G-F 25 g
 $164.00
1/EA		 Add To Favorites
45-04936-100G-F 100 g
 $261.00
1/EA		 Add To Favorites

 

application(s) peptide synthesis
assay ≥98.0% (HPLC)
form powder
functional group amine
  chloro
impurities ≤0.5% water
InChI 1S/C11H15ClN5O.F6P/c1-15(2)11(16(3)4)18-17-10-7-8(12)5-6-9(10)13-14-17;1-7(2,3,4,5)6/h5-7H,1-4H3;/q+1;-1
InChI key ZHHGTMQHUWDEJF-UHFFFAOYSA-N
mp 185-190 °C
Quality Level 200 
reaction suitability reaction type: Coupling Reactions
SMILES string ClC1=CC=C(N([C+](N(C)C)N(C)C)N=[N+]2[O-])C2=C1.F[P-](F)(F)(F)(F)F
Application: Reagent for:
Synthesis of near-infrared pH activatable fluorescent probes
Synthesis of human β-amyloid by Fmoc chemistry
Stereoselective Horner-Wadsworth-Emmons olefination
Covalent ligation of fluorescent peptides to quantum dots
Alkylation of human telomere sequence
Other Notes: Tandem Oligonucleotide Synthesis on Solid-Phase Supports for the Production of Multiple Oligonucleotides
Symbol GHS02  GHS02
Signal word Danger
Hazard statements H228
Precautionary statements P210
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)
mp 185-190 °C
UNSPSC 12352101

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