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16536-30-4

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16536-30-4 Usage

Chemical Properties

light yellow powder

Uses

Bis(2,4-dinitrophenyl) oxalate was used in detection of fluorescent compound dansylalanine in buffer solution by flow injection analysis.

General Description

Bis(2,4-dinitrophenyl) oxalate (DNPO) is a chemiluminescence reagent. Chemiluminescence produced in the oxidation of DNPO by hydrogen peroxide in the presence of a polycyclic aromatic hydrocarbon was monitored by spectroscopic methods. The kinetics of the imidazole-catalyzed decomposition of DNPO was investigated by the stopped-flow technique.

Check Digit Verification of cas no

The CAS Registry Mumber 16536-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,3 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16536-30:
(7*1)+(6*6)+(5*5)+(4*3)+(3*6)+(2*3)+(1*0)=104
104 % 10 = 4
So 16536-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H6N4O12/c19-13(29-11-3-1-7(15(21)22)5-9(11)17(25)26)14(20)30-12-4-2-8(16(23)24)6-10(12)18(27)28/h1-6H

16536-30-4 Well-known Company Product Price

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  • Aldrich

  • (325376)  Bis(2,4-dinitrophenyl)oxalate  98%

  • 16536-30-4

  • 325376-1G

  • 1,777.23CNY

  • Detail

16536-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name BIS(2,4-DINITROPHENYL) OXALATE

1.2 Other means of identification

Product number -
Other names bis(2,4-dinitrophenyl)oxalate

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:16536-30-4 SDS

16536-30-4Related news

Pre-Chemiluminescent biexponential degradation of bis(2,4-dinitrophenyl) oxalate in hydrogen peroxide-acetonitrile08/11/2019

The pre-chemiluminescent hydrogen peroxide-bis(2,4-dinitrophenyl) oxalate reaction has been studied in order to understand better its role in peroxyoxalate chemiluminescence. The reaction is shown to be first order in each reactant. An unusual biexponential degradation of the oxalate occurs whic...detailed

Unexpected decomposition in the reaction of bis(2,4-dinitrophenyl) oxalate with water08/10/2019

The kinetics of the hydrolysis of bis(2,4-dinitrophenyl) oxalate (DNPO) were studied by infrared spectroscopy. The changes in the carbonyl region showed that neither 2,4-dinitrophenyl hydrogen oxalate nor oxalic acid could be detected. Simultaneously, the rate of evolution of carbon dioxide was ...detailed

16536-30-4Relevant articles and documents

Hydrogen peroxide responsive compound for imaging and therapy and synthetic method thereof

-

Paragraph 0091-0093, (2020/09/16)

The invention discloses a hydrogen peroxide responsive compound for imaging and therapy and a synthetic method thereof. The chemical structure of the responsive compound is shown in the following figure defined in the specification. The invention also pro

The Hammett correlation between distyrylbenzene substituents and chemiluminescence efficiency providing various ρ-values for peroxyoxalate chemiluminescence of several oxalates

Maruyama, Takayuki,Narita, Susumu,Motoyoshiya, Jiro

, p. 222 - 231 (2013/03/13)

Peroxyoxalate chemiluminescence (PO-CL) was investigated using eight oxalates with various phenol moieties and the distyrylbenzene (DSB) fluorophores with various substituents. The ρ-values in the Hammett correlation between the substituent constants (σp+) of the DSBs and the singlet chemiexcitation yields (ΦS) for the PO-CL reactions varied from -0.50 to -1.01 depending on the oxalate structure, and the reactive oxalates tended to afford the higher absolute ρ-values but with a few exceptions. Based on the CIEEL mechanism, these experimental observations suggest that the aryloxy groups still remain in the 1,2-dioxetanones (DOTs), which are the postulated high-energy intermediates, and control the electronic properties of DOTs as electron-acceptors. The LUMO energies of the DOTs calculated by the ab initio method with a B3LYP/6-31g(d) basis set reveal that the lower the DOT-LUMO energies, the higher the absolute ρ-values were provided for the corresponding oxalates, as predicted by the frontier molecular orbital (FMO) theory. Thus, the chemical species interacting with the DSBs would be not unitary and will be DOTs.

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