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Methyl tris(4-nitrophenyl)-phosphonium bromide, also known as MTNP, is a chemical compound with the formula C20H15N3O6PBr. It is a yellow crystalline solid that is soluble in organic solvents such as acetone, chloroform, and dioxane. MTNP is a phosphonium salt, which is a type of organophosphorus compound. It is commonly used as a phase-transfer catalyst in organic synthesis, facilitating reactions between organic and inorganic compounds. The compound is also known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. Due to its reactivity and the presence of nitro groups, it is important to handle MTNP with care, as it can be sensitive to heat and friction.

3016-87-3

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3016-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3016-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3016-87:
(6*3)+(5*0)+(4*1)+(3*6)+(2*8)+(1*7)=63
63 % 10 = 3
So 3016-87-3 is a valid CAS Registry Number.

3016-87-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Tris(4-nitrophenyl)methyl radical

1.2 Other means of identification

Product number -
Other names Tri(p-nitrophenyl)methyl Radikal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3016-87-3 SDS

3016-87-3Downstream Products

3016-87-3Relevant academic research and scientific papers

Doping of an organic molecular semiconductor by substitutional cocrystallization with a molecular n-dopant

Porter Jr., William W.,Vaid, Thomas P.

, p. 469 - 475 (2008/02/03)

Dopants for organic molecular semiconductors that yield immobile dopant ions are necessary for the creation of stable molecular semiconductor p-n junctions, the basis for almost all traditional inorganic semiconductor devices. We present evidence for the substitutional cocrystallization of tris(4-nitrophenyl)methyl radical (1) with small amounts of tris[4- (dimethylamino)phenyl]methyl radical (2), resulting in n-doped 1 with immobile 2+ counterions. Cyclic voltammetry indicates that electron transfer from 2 to 1 is favored by 0.51 eV. The powder X-ray diffraction patterns of pure 1 and 1 doped with 2 are very similar, indicating substitutional cocrystallization. The electrical conductivity of doped 1 increases with increasing concentration of 2, and the conductivity is constant over time. Variable-temperature conductivity measurements of 1 doped with 2% and 5% 2 indicate that the activation energy of conduction is 0.32 eV at both dopant concentrations. The Royal Society of Chemistry 2007.

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