Dipropalin

Base Information

Chemical Name:Dipropalin
CAS No.:1918-08-7
Molecular Formula:C₁₃H₁₉N₃O₄
Molecular Weight:281.312
Hs Code.:
UNII:389074G62J
DSSTox Substance ID:DTXSID1041895
Nikkaji Number:J7.813A
Wikidata:Q27256766
Metabolomics Workbench ID:144319
Mol file:1918-08-7.mol

Synonyms:DIPROPALIN;1918-08-7;2,6-Dinitro-N,N-dipropyl-p-toluidine;4-methyl-2,6-dinitro-N,N-dipropylaniline;Caswell No. 391C;Benzenamine, 4-methyl-2,6-dinitro-N,N-dipropyl-;EPA Pesticide Chemical Code 391400;N,N-Dipropyl-2,6-dinitro-p-toluidine;BRN 2816199;p-Toluidine, 2,6-dinitro-N,N-dipropyl-;2,6-Dinitro-N,N-di-n-propyl-p-toluidine;389074G62J;N,N-Di-n-propyl-2,6-dinitro-4-methylaniline;DIPROPALIN [MI];SCHEMBL1876519;DTXSID1041895;UNII-389074G62J;3,5-DINITRO-4-DIPROPYLAMINOTOLUENE;LS-154370;N,N-di(n-propyl)-2,6-dinitro-4-methylaniline;1-12-00-00443 (Beilstein Handbook Reference);2,6-DINITRO-N,N-DIPROPYL-4-METHYLANILINE;L-35355;N,N-DIPROPYL-2,6-DINITRO-4-METHYLANILINE;4-METHYL-2,6-DINITRO-N,N-DIPROPYLBENZENAMINE;Q27256766

Suppliers and Price of Dipropalin

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 7 raw suppliers

Chemical Property of Dipropalin

Chemical Property:

Vapor Pressure:5.74E-07mmHg at 25°C
Melting Point:80°
Boiling Point:411.1°Cat760mmHg
PKA:1.31±0.50(Predicted)
Flash Point:202.4°C
PSA：94.88000
Density:1.205g/cm³
LogP:4.48420
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:281.13755610
Heavy Atom Count:20
Complexity:310

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCN(CCC)C1=C(C=C(C=C1[N+](=O)[O-])C)[N+](=O)[O-]
Uses Herbicide.

Technology Process of Dipropalin

There total 2 articles about Dipropalin 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: