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760952-88-3

760952-88-3 Structure

760952-88-3 Structure
IdentificationBack Directory
[Name]

Tris(3-hydroxypropyltriazolylMethyl)aMine 95%
[CAS]

760952-88-3
[Synonyms]

THPTA
Tris(3-hydroxypropyltriazolylMethyl)a
tris(3-hydroxypropyltriazolymethyl)amine
Tris(3-hydroxypropyltriazolylmethyl)amine
Tris(3-hydroxypropyltriazolylMethyl)aMine95%
Tris(3-hydroxypropyltriazolylMethyl)aMine 95%
4,4',4''-Nitrilotris(4-(1H-1,2,3-triazol-4-yl)butan-1-ol)
Tris[[1-(3-hydroxypropyl)-1H-1,2,3-triazol-4-yl]methyl]amine
1H-1,2,3-Triazole-1-propanol, 4,4',4''-[nitrilotris(methylene)]tris-
3,3′,3′′-(4,4′,4′′-(Nitrilotris(methylene))tris(1H-1,2,3-triazole-4,1-diyl))tris(propan-1-ol)
3,3',3''-((4,4'4,”-nitrilotris(methylene))tris(1H-1,2,3-triazole-5,1-diyl))tris(propan-1-ol) -(THPTA)
[Molecular Formula]

C18H30N10O3
[MDL Number]

MFCD27665386
[MOL File]

760952-88-3.mol
[Molecular Weight]

434.496
Chemical PropertiesBack Directory
[Melting point ]

331-336°C (decomposition)
[Boiling point ]

723.8±70.0 °C(Predicted)
[density ]

1.44±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO (Slightly), Methanol (Very Slightly)
[form ]

Solid
[pka]

14.34±0.10(Predicted)
[color ]

White to Off-White
[Appearance]

White or light grey solid
[InChI]

InChI=1S/C18H30N10O3/c29-7-1-4-26-13-16(19-22-26)10-25(11-17-14-27(23-20-17)5-2-8-30)12-18-15-28(24-21-18)6-3-9-31/h13-15,29-31H,1-12H2
[InChIKey]

VAKXPQHQQNOUEZ-UHFFFAOYSA-N
[SMILES]

N(CC1N=NN(CCCO)C=1)(CC1N=NN(CCCO)C=1)CC1N=NN(CCCO)C=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2933.99.9701
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Description]

THPTA is a water-soluble, very effective ligand for Cu(I)-catalyzed Alkyne-Azide click chemistry reactions (CuAAC). It serves a dual purpose: 1) Acceleration of the CuAAC reaction by maintaining the Cu(I) oxidation state of copper sources and 2) Protection of biomolecules from oxidative damage during the labeling reaction. THPTA is a superior alternative to water-insoluble TBTA. a) J. Am. Chem. Soc. 2011, 133, 17993. b) Bioconjugate Chem. 2010, 21, 1912.
[Uses]

Tris(3-hydroxypropyltriazolylmethyl)amine when complexed to copper(I) can be used as a catalyst.
[reaction suitability]

reaction type: click chemistry
[storage]

Store at -20°C
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