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63556-80-9

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63556-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63556-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63556-80:
(7*6)+(6*3)+(5*5)+(4*5)+(3*6)+(2*8)+(1*0)=139
139 % 10 = 9
So 63556-80-9 is a valid CAS Registry Number.

63556-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,3,5-tricarboperoxoic acid

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetricarboperoxoic acid

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:63556-80-9 SDS

63556-80-9Downstream Products

63556-80-9Relevant articles and documents

Highly Energetic, Low Sensitivity Aromatic Peroxy Acids

Gamage, Nipuni-Dhanesha H.,Stiasny, Benedikt,Stierstorfer, J?rg,Martin, Philip D.,Klap?tke, Thomas M.,Winter, Charles H.

, p. 2582 - 2585 (2016)

The synthesis, structure, and energetic materials properties of a series of aromatic peroxy acid compounds are described. Benzene-1,3,5-tris(carboperoxoic) acid is a highly sensitive primary energetic material, with impact and friction sensitivities similar to those of triacetone triperoxide. By contrast, benzene-1,4-bis(carboperoxoic) acid, 4-nitrobenzoperoxoic acid, and 3,5-dinitrobenzoperoxoic acid are much less sensitive, with impact and friction sensitivities close to those of the secondary energetic material 2,4,6-trinitrotoluene. Additionally, the calculated detonation velocities of 3,5-dinitrobenzoperoxoic acid and 2,4,6-trinitrobenzoperoxoic acid exceed that of 2,4,6-trinitrotoluene. The solid-state structure of 3,5-dinitrobenzoperoxoic acid contains intermolecular O-H?O hydrogen bonds and numerous N?O, C?O, and O?O close contacts. These attractive lattice interactions may account for the less sensitive nature of 3,5-dinitrobenzoperoxoic acid.

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