Hydrazine, N,N'-dimethyl-N,N'-dipentyl-

Base Information

• Chemical Name: Hydrazine, N,N'-dimethyl-N,N'-dipentyl-
• CAS No.: 106376-59-4
• Molecular Formula: C12H28 N2
• Molecular Weight: 200.368
• DSSTox Substance ID: DTXSID10147591
• Nikkaji Number: J1.630.006C
• Wikidata: Q83012953
• Mol file: 106376-59-4.mol

Synonyms:Hydrazine, N,N'-dimethyl-N,N'-dipentyl-;106376-59-4;1,2-dimethyl-1,2-dipentylhydrazine;DTXSID10147591

Chemical Property of Hydrazine, N,N'-dimethyl-N,N'-dipentyl-

Chemical Property:

• Vapor Pressure: 0.0186mmHg at 25°C
• Boiling Point: 253.1°Cat760mmHg
• Flash Point: 93.3°C
• Density: 0.83g/cm³
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 9
• Exact Mass: 200.225248902
• Heavy Atom Count: 14
• Complexity: 101

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCN(C)N(C)CCCCC

Technology Process of Hydrazine, N,N'-dimethyl-N,N'-dipentyl-

There total 2 articles about Hydrazine, N,N'-dimethyl-N,N'-dipentyl- 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:

pentanal (110-62-3) + N,N'-Dimethylhydrazine dihydrochloride (306-37-6) → 1,2-di-n-pentyldimethylhydrazine (106376-59-4)

Guidance literature:

With sodium tetrahydroborate; N,N-dimethyl-ethanamine; acetic acid; Yield given. Multistep reaction; 1.) acetnitrile, 30 min, 2.) acetonitrile, r.t.;

DOI:10.1021/ja00232a001

Reference yield:

octahydro-[1,1']bipyrrolyl (18389-95-2) + 1,2-di-n-pentyldimethylhydrazine cation radical (106376-60-7) → N,N'-Dipiperidin-Kation-Radikal (106376-69-6) + 1,2-di-n-pentyldimethylhydrazine (106376-59-4)

Guidance literature:

In chloroform; benzene; at 276.9 ℃; Kinetics; Thermodynamic data; ΔG(excit); insitu ionization;

DOI:10.1021/ja00239a015

Reference yield:

1,2-di-n-pentyldimethylhydrazine (106376-59-4) + tetramethylhydrazine cation radical (6415-12-9,14213-69-5) → tetramethylhydrazine (6415-12-9) + 1,2-di-n-pentyldimethylhydrazine cation radical (106376-60-7)

Guidance literature:

In chloroform; benzene; at 276.9 ℃; Rate constant; Thermodynamic data; ΔG(excit); insitu ionization;

DOI:10.1021/ja00239a015

upstream raw materials:

octahydro-[1,1']bipyrrolyl

1,2-di-n-pentyldimethylhydrazine cation radical

pentanal

N,N'-Dimethylhydrazine dihydrochloride

Downstream raw materials:

tetramethylhydrazine

1,2-di-n-pentyldimethylhydrazine cation radical

dimethyl-piperidin-1-yl-amine

1,2-Dipropyl-1,2-dimethylhydrazin

Refernces

• 1、 Nelsen, Stephen F.,Rumack, Daniel T.,Meot-Ner (Mautner), Michael. "Kinetic Effects of an Unusually Large Neutral to Radical Cation Geometry Change. Slow Electron-Transfer Reactions between Alkylhydrazines". . p. 1373 - 1379. Retrieved 2007/10/02.