N,N,N,N-Tetraethyl-1,3-propanediamine
Product Information
Molecular Formula
(C2H5)2N(CH2)3N(C2H5)2
Molecular Weight
186.34
Description
N,N,N,N-Tetraethyl-1,3-propanediamine is a biomedical product extensively employed in the development of pharmaceuticals and chemical research. It plays a crucial role as a reactant and catalyst in various processes. This compound is utilized in the synthesis of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Its versatile applications in biomedicine make it an indispensable tool for scientific advancements and drug discovery.
Synonyms
N,N,N',N'-tetraethylpropane-1,3-diamine; N,N,N',N'-Tetraethyl trimethylene diamine; 1,3-Propanediamine, N,N,N',N'-tetraethyl-; N1,N1,N3,N3-tetraethylpropane-1,3-diamine; 1,3-bis(diethylamino)propane; 3,5-BIS[2-(BOC-AMINO)ETHOXY]-BENZOICACID; N,N,N',N'-Tetraethyl-1,3-propanediamine, 97%
IUPAC Name
N,N,N',N'-tetraethylpropane-1,3-diamine
SMILES
CCN(CC)CCCN(CC)CC
InChI
InChI=1S/C11H26N2/c1-5-12(6-2)10-9-11-13(7-3)8-4/h5-11H2,1-4H3
InChI Key
RCZLVPFECJNLMZ-UHFFFAOYSA-N
Boiling Point
133 °C/80 mmHg (lit.)
Flash Point
168.8 °CF - closed cup
Purity
0.97
Density
0.81 g/mL at 25 °C (lit.)
Refractive Index
n20/D 1.4377 (lit.)
Safety Information
Hazards
H314
Precautionary Statement
P280 - P305 + P351 + P338 - P310
Computed Properties
XLogP3
2.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
8
Exact Mass
186.209598838 g/mol
Monoisotopic Mass
186.209598838 g/mol
Topological Polar Surface Area
6.5Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
84.3
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| AU-2021106603-A4 | Hyperbranched polyester modified carbon nanotube modified epoxy pitch and preparation method thereof | 2021-08-23 |
| CN-113070045-A | Preparation method of adsorbent for removing nitrate in industrial wastewater | 2021-04-29 |
| US-2022033571-A1 | Polycyloolefinic polymers and anion exchange membranes derived therefrom | 2020-07-30 |
| JP-7005089-B1 | Easy-to-disassemble adhesive materials, hardened materials, articles and dismantling methods | 2020-07-08 |
| WO-2022009513-A1 | Adhesive material for easy disassembly, cured object, article, and disassembly method | 2020-07-08 |
| US-2022002469-A1 | Polyol compositions and methods | 2020-06-24 |
| WO-2021262845-A1 | Polyol compositions and methods | 2020-06-24 |
| JP-2021194567-A | Composition for carbon dioxide separation, and method for separating carbon dioxide | 2020-06-10 |
| WO-2021174522-A1 | A method for the alkylation of amines | 2020-03-06 |
| WO-2021174523-A1 | A method for preparing alkylated amines | 2020-03-06 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 16848427 | 2006-07-26 | Reversible O-O bond cleavage in copper-dioxygen isomers: impact of anion basicity | Journal of the American Chemical Society |
