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Bis(2,2,2-trinitroethyl)-phtalate, also known as dinitroethyl phthalate, is a chemical compound with the formula C16H16N2O12. It is derived from phthalic acid, an organic compound commonly used in the production of plasticizers. In Bis(2,2,2-trinitroethyl)-phtalate, two 2,2,2-trinitroethyl groups are attached to the phthalate molecule, resulting in a highly energetic and potentially explosive substance. Due to its chemical structure, it exhibits properties such as high density, low melting point, and high sensitivity to impact and friction. This makes it a potential candidate for use in military applications, such as explosives and propellants. However, its handling and storage require extreme caution due to its hazardous nature and potential for accidental detonation.

6093-30-7

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6093-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6093-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6093-30:
(6*6)+(5*0)+(4*9)+(3*3)+(2*3)+(1*0)=87
87 % 10 = 7
So 6093-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N6O16/c19-9(33-5-11(13(21)22,14(23)24)15(25)26)7-3-1-2-4-8(7)10(20)34-6-12(16(27)28,17(29)30)18(31)32/h1-4H,5-6H2

6093-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(2,2,2-trinitroethyl) phthalate

1.2 Other means of identification

Product number -
Other names Phthalsaeure-bis-(2,2,2-trinitro-aethylester)

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:6093-30-7 SDS

6093-30-7Downstream Products

6093-30-7Relevant academic research and scientific papers

Sterically Hindered Carboxylic Acid Esters

Bagal,Ishchenko,Nikolaev

, p. 1731 - 1738 (2007/10/03)

Methods have been developed for preparation of esters formed by sterically hindered benzoic acids and various alcohols, which were difficult to obtain previously. The methods are based on the reaction of carbenium ions, generated from primary aliphatic N-nitroamines by the action of nitrous acid or Lewis acids, with carboxylic acid at the sterically accessible oxygen atom of the carboxy group. Reactions of nitrobenzoic acids and benzenepolycarboxylic acids with 2,2,2-trinitroethyl hydrogen sulfate provide an effective method for preparation of corresponding trinitroethyl esters.

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