1,6-Hexanediamine, N,N-diethyl-

Base Information

Chemical Name:1,6-Hexanediamine, N,N-diethyl-
CAS No.:13029-29-3
Molecular Formula:C10H24N2
Molecular Weight:172.314
Hs Code.:
DSSTox Substance ID:DTXSID30427968
Wikidata:Q82240726

Synonyms:13029-29-3;1,6-Hexanediamine, N1,N1-diethyl-;N1,N1-Diethylhexane-1,6-diamine;1,6-Hexanediamine, N,N-diethyl-;(6-AMINOHEXYL)DIETHYLAMINE;SCHEMBL578556;RHODIZONICACIDDISODIUMSALT;DTXSID30427968;MFCD06446913;AKOS000257075;A909074

Suppliers and Price of 1,6-Hexanediamine, N,N-diethyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 1,6-Hexanediamine, N,N-diethyl-

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:172.193948774
Heavy Atom Count:12
Complexity:79.9

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CCCCCCN

Technology Process of 1,6-Hexanediamine, N,N-diethyl-

There total 2 articles about 1,6-Hexanediamine, N,N-diethyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 124-09-4
1,6-Hexanediamine

: 64-17-5
ethanol

: 40043-26-3
N-ethylhexane-1,6-diamine

: 13093-05-5
N,N'-diethylhexamethylenediamine

: 13029-29-3
N,N-diethylhexane-1,6-diamine

Guidance literature:: With hydrogen; at 200 ℃; for 8h; under 7500.75 Torr; Product distribution / selectivity;

Reference yield:

: 63945-11-9
6-phthalimido-1-hexanol

: 13029-29-3
N,N-diethylhexane-1,6-diamine

Guidance literature:: Multi-step reaction with 3 steps

1: CBr₄; PPh₃ / acetonitrile / 20 °C

2: K₂CO₃ / dioxane / 20 °C

3: H₂NNH₂ / methanol / 20 °C

With carbon tetrabromide; potassium carbonate; triphenylphosphine; hydrazine; In 1,4-dioxane; methanol; acetonitrile;
DOI:10.1016/j.bmcl.2004.05.090