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N,2,4,6-tetranitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4591-46-2

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4591-46-2 Usage

Safety Profile

The impure material deflagrates (burns explosively) when heated to 50°C. When heated to decomposition it emits toxic fumes of NOx. See also NITRO COMPOUNDS of AROMATIC HYDROCARBONS.

Check Digit Verification of cas no

The CAS Registry Mumber 4591-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4591-46:
(6*4)+(5*5)+(4*9)+(3*1)+(2*4)+(1*6)=102
102 % 10 = 2
So 4591-46-2 is a valid CAS Registry Number.

4591-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4,6-trinitrophenyl)nitramide

1.2 Other means of identification

Product number -
Other names 2.4.6-Trinitro-diazobenzolsaeure

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:4591-46-2 SDS

4591-46-2Downstream Products

4591-46-2Relevant academic research and scientific papers

A Stable Hexakis(guanidino)benzene: Realization of the Strongest Neutral Organic Four-Electron Donor

Eberle, Benjamin,Kaifer, Elisabeth,Himmel, Hans-J?rg

supporting information, p. 3360 - 3363 (2017/03/17)

The growing demand for efficient batteries has stimulated the search for redox-active organic compounds with multistage redox behavior, as materials with large charge capacity. Herein we report the synthesis and properties of the first hexakis(guanidino)benzene derivative: a strong neutral organic electron donor with reversible multistage redox behavior and a record low redox potential for donation of four electrons. Detailed structural and spectroscopic characterization of three redox states (0, +2, and +4) reveal its unique electronic features. Despite its nitrogen richness, the compound is thermally robust and can be readily purified by sublimation.

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