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Naphthalene, 1,3,5-trinitro-

Base Information Edit
  • Chemical Name:Naphthalene, 1,3,5-trinitro-
  • CAS No.:2243-94-9
  • Molecular Formula:C10H5 N3 O6
  • Molecular Weight:263.166
  • Hs Code.:2904209090
  • DSSTox Substance ID:DTXSID9075296
  • Nikkaji Number:J134.715B
  • Wikidata:Q82003289
  • Mol file:2243-94-9.mol
Naphthalene, 1,3,5-trinitro-

Synonyms:1,3,5-trinitronaphthalene;NAPHTHALENE, 1,3,5-TRINITRO-;2243-94-9;1,3,5-Trinitronaphthalene [Forbidden];SCHEMBL9119541;DTXSID9075296;C10H5N3O6;NA0217

Suppliers and Price of Naphthalene, 1,3,5-trinitro-
Supply Marketing:Edit
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 4 raw suppliers
Chemical Property of Naphthalene, 1,3,5-trinitro- Edit
Chemical Property:
  • Vapor Pressure:5.16E-08mmHg at 25°C 
  • Melting Point:124°C 
  • Refractive Index:1.4830 (estimate) 
  • Boiling Point:454.4°Cat760mmHg 
  • Flash Point:236°C 
  • PSA:137.46000 
  • Density:1.654g/cm3 
  • LogP:4.13400 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:263.01783489
  • Heavy Atom Count:19
  • Complexity:398
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C(C=C(C=C2[N+](=O)[O-])[N+](=O)[O-])C(=C1)[N+](=O)[O-]
  • Uses Explosive, stabilizer for nitrocellulose.
Technology Process of Naphthalene, 1,3,5-trinitro-

There total 6 articles about Naphthalene, 1,3,5-trinitro- 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:
Guidance literature:
With nitric acid; at 110 ℃; Behandeln des Reaktionsprodukts mit Alkohol;
upstream raw materials:

1,5-dinitronaphthalene

nitric acid

Downstream raw materials:

3,5-dinitrophthalic acid

3-nitrophthalic acid

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