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19059-14-4

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19059-14-4 Usage

Definition

ChEBI: The nitrogen oxoanion formed by loss of a proton from peroxynitrous acid.

Safety Profile

Questionable carcinogen with experimental carcinogenic data reported. Whenheated to decomposition it emits toxic vapors of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 19059-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19059-14:
(7*1)+(6*9)+(5*0)+(4*5)+(3*9)+(2*1)+(1*4)=114
114 % 10 = 4
So 19059-14-4 is a valid CAS Registry Number.
InChI:InChI=1/HNO3/c2-1-4-3/h3H/p-1

19059-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name peroxynitrite

1.2 Other means of identification

Product number -
Other names Peroxonitrite

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:19059-14-4 SDS

19059-14-4Relevant articles and documents

Cold atmospheric plasma activated water as a prospective disinfectant: The crucial role of peroxynitrite

Zhou, Renwu,Zhou, Rusen,Prasad, Karthika,Fang, Zhi,Speight, Robert,Bazaka, Kateryna,Ostrikov, Kostya

supporting information, p. 5276 - 5284 (2018/12/05)

The socio-economic, environmental, and health implications of diseases caused by pathogenic microorganisms and their treatment using conventional antimicrobials are significant. The increasing resistance to antibiotics and detrimental biological side effects of many common antibiotics on human health and on the ecosystem have driven the search for new cost-effective and highly-efficient sterilization treatments and agents that are more environmentally benign. Plasma activated water (PAW), a product of cold atmospheric plasma reacting with water, is a promising broad-spectrum biocidal agent whose biochemical activity is attributed to the presence of a rich diversity of highly reactive oxygen and nitrogen species (RONS). The transient activity of PAW, where PAW reverts to water within days of storage and application, suggests that it can become a green alternative to conventional chemical treatment methods, yet the issues of scale up and the not fully understood mechanism of activity remain. In this study, we sought to explore the antibiotic potential of PAW generated from a plasma jet in a continuous flow reactor and determine the individual and combined contribution of thus-generated reactive chemistries in PAW for organism inactivation. Treatment of Escherichia coli with PAW led to more than a 4-log reduction, while exposure to an equivalent single dose of hydrogen peroxide (H2O2), nitrate (NO3-) or nitrite (NO2-) to that found in PAW failed to attain the same level of reduction. Peroxynitrite was identified as a critical bioactive species, particularly under acidic conditions, originating from the synergistic plasma effects (like the reactions of H2O2, NO3-, NO2- and other existing short-lived species like OH radicals in PAW). This research successfully demonstrated the possibility of PAW being an effective environmentally benign disinfectant, the activity of which is closely linked to the generation of peroxynitrite, providing much needed insights into the fundamental aspects of PAW chemistry required for optimisation of the biochemical activity of PAW and translation of this decontamination strategy into real life applications.

The Primary Photodynamics of Aqueous Nitrate: Formation of Peroxynitrite

Madsen, Dorte,Larsen, Jane,Jensen, Svend Knak,Keiding, Soren R.,Thogersen, Jan

, p. 15571 - 15576 (2007/10/03)

We have examined the photochemical reactions occurring after irradiation at 200 nm of the aqueous nitrate ion, NO3-(aq). Using femtosecond transient absorption spectroscopy over the range 194-388 nm, we have characterized the formation and subsequent relaxation of the primary photoproducts of nitrate photolysis. The dominant photoproduct is the cis-isomer of peroxynitrite, which accounts for 48% of the excited state molecules initially produced. A slightly smaller fraction, 44%, of the excited molecules return to the electronic ground state of NO3- and relax to the vibrational ground state in 2 ps. The remaining 8% of the molecules initially excited react via the ?NO + ?O2 - or the NO- + O2 dissociation channels. Formation of NO2- and ?NO2 is not observed, suggesting that the previous observations of these species in steady-state photolysis are caused by reactions occurring on a longer time scale.

Photolysis of the N=N bond in trioxodinitrate: Reaction between triplet NO- and O2 to form peroxonitrite [4]

Donald, Caroline E.,Hughes, Martin N.,Thompson, Janet M.,Bonner, Francis T.

, p. 2676 - 2677 (2008/10/08)

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