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


45-04936-5G-F	5 g	$33.40 1/EA	Add To Favorites
45-04936-25G-F	25 g	$159.00 1/EA	Add To Favorites
45-04936-100G-F	100 g	$253.00 1/EA	Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

application(s)	peptide synthesis
assay	≥98.0% (HPLC)
form	powder
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
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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