lead 2,4,6-trinitro-m-phenylene dioxide

Base Information

• Chemical Name: lead 2,4,6-trinitro-m-phenylene dioxide
• CAS No.: 15245-44-0
• Molecular Formula: C₆HN₃O₈*Pb
• Molecular Weight: 450.289
• Mol file: 15245-44-0.mol

Synonyms:2,4-Dioxa-3-plumbabicyclo[3.3.1]nona-1(9),5,7-triene,3,3-didehydro-6,8,9-trinitro- (7CI); Lead, [styphnato(2-)]- (6CI); Resorcinol,2,4,6-trinitro-, lead(2+) salt (1:1) (8CI); Lead styphnate; Lead tricinate;Lead trinitroresorcinate; Tricinat

Chemical Property of lead 2,4,6-trinitro-m-phenylene dioxide

Chemical Property:

• Appearance/Colour: hexagonal platelets
• Boiling Point: 292.6°Cat760mmHg
• Flash Point: 126.8°C
• PSA: 155.92000
• Density: g/cm³
• LogP: 2.28620

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Hazard Codes: E,T,N
• Statements: 61-3-20/22-33-50/53-62
• Safety Statements: 53-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Description: Pure tetraethyl lead is a colourless liquid with a characteristic odour and is a viscous liquid that is highly lipophilic and soluble in fats, oils, and lipids as well as gasoline and other nonpolar hydrocarbons. Tetraethyl lead is commonly abbreviated as TEL. Tetraethyl lead is an organolead compound, and it improves the efficiency and performance of internal combustion engines and is an inexpensive additive to gasoline (petrol) since 1920 and allows octane ratings and engine compression to be boosted significantly, increasing power and fuel economy. The use of tetraethyl lead was largely discontinued because of the toxicity of lead and its deleterious effect on catalytic converters.
• Uses: Lead Styphnate is an explosive compound used in primers and detonator mixtures for less sensitive secondary explosives.

Technology Process of lead 2,4,6-trinitro-m-phenylene dioxide

There total 3 articles about lead 2,4,6-trinitro-m-phenylene dioxide 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:

styphnic acid (82-71-3) → lead styphnate (15245-44-0,17992-50-6)

Guidance literature:

With water; lead(II) oxide;

Reference yield:

→ monobasic lead styphnate (15245-44-0,17992-50-6)

Guidance literature:

With lead(II) nitrate; at 95 - 100 ℃;

Reference yield:

lead(II) nitrate + sodium styphnate → monobasic lead styphnate (15245-44-0,17992-50-6)

Guidance literature:

In water; soln. of Pb(NO3)2 added to agitated soln. of sodium styphnate, pre-heated to 95°C; ppt. filtered hot; washed (H2O, alc.); dried under vac. in desiccator over silica gel (25 h); elem. anal.;

DOI:10.1016/0040-6031(94)85003-8

upstream raw materials:

styphnic acid