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Assay
97%
form
liquid
refractive index
n20/D 1.436 (lit.)
bp
42-43 °C/12 mmHg (lit.)
density
0.838 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
CN(C)C(N(C)C)N(C)C
InChI
1S/C7H19N3/c1-8(2)7(9(3)4)10(5)6/h7H,1-6H3
InChI key
MUMVIYLVHVCYGI-UHFFFAOYSA-N
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General description
NMR spectra and their temperature-dependence has been reported for tris(dimethylamino)methane. Tris(dimethylamino)methane reacts with crowded α-(o-nitrophenyl) ketone to yield tetrahydroquinoline derivative.
Application
Tris(dimethylamino)methane was used:
- to prepare the phosphoramidite derivative of the new nucleoside analog
- as reagent for the introduction of the dimethylaminoethylidene group
- in ring-opening (RO) polymerization of lactide
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
Advanced Synthesis & Catalysis, 346, 1081-1081 (2004)
yDNA: a new geometry for size-expanded base pairs.
Angewandte Chemie (International ed. in English), 43(43), 5834-5836 (2004-11-04)
Tetrahedron, 45, 6631-6631 (1989)
Conformational Dynamics of Triple Rotors: Tris (dimethylamino) methane, Triisopropylamine, and Related Molecules1.
The Journal of Organic Chemistry, 61(4), 1290-1296 (1996)
Sci. Synth., 22, 795-795 (2005)
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