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Merck

N24609

Nitrosobenzene

greener alternative

≥97%

Sinónimos:

NOB

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About This Item

Fórmula empírica (notación de Hill):
C6H5NO
Número CAS:
586-96-9
Peso molecular:
107.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24897573
EC Number:
209-591-1
Beilstein/REAXYS Number:
605688
MDL number:
MFCD00002059

Nombre del producto

Nitrosobenzene, ≥97%

InChI key

NLRKCXQQSUWLCH-UHFFFAOYSA-N

InChI

1S/C6H5NO/c8-7-6-4-2-1-3-5-6/h1-5H

SMILES string

O=Nc1ccccc1

assay

≥97%

form

solid

greener alternative product score

old score: 51
new score: 16
Find out more about DOZN™ Scoring

greener alternative product characteristics

Safer Solvents and Auxiliaries
Design for Energy Efficiency
Inherently Safer Chemistry for Accident Prevention
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

bp

59 °C/18 mmHg (lit.)

mp

65-69 °C (lit.)

greener alternative category

, Re-engineered

storage temp.

2-8°C

Quality Level

100

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Application

Spin trap reagent. Has been used in the study of oxidative DNA damage and nitroso-compound-induced respiratory burst in neutrophils.
Spin trap. Undergoes various addition, reduction, and oxidation reactions.

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Safer Solvents and Auxiliaries”, “Enhanced Energy Efficiency” and “Inherently Safer Chemistry for Accident Prevention”. Click here to view its DOZN scorecard.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
STBK5165
STBH9196
STBF8537V
STBD9891V
STBC8555V

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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

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Karol Trojanowicz et al.
Environmental technology, 42(7), 1023-1037 (2019-09-03)
An explanation of possible mechanism of efficient PN/A in hybrid bioreactors was presented. The bottleneck process is nitritation. Surplus nitrite production by ammonium oxidizing bacteria (AOB) is required for assuring the activity of anammox bacteria and eliminating nitrite oxidizing bacteria
Zachary J Buras et al.
Physical chemistry chemical physics : PCCP, 20(19), 13191-13214 (2018-05-04)
The C9H11 potential energy surface (PES) was experimentally and theoretically explored because it is a relatively simple, prototypical alkylaromatic radical system. Although the C9H11 PES has already been extensively studied both experimentally (under single-collision and thermal conditions) and theoretically, new
Xiuzhen Shi et al.
Environmental microbiology, 19(12), 4851-4865 (2017-07-29)
Soil ecosystem represents the largest contributor to global nitrous oxide (N
Eva Spieck et al.
Frontiers in microbiology, 11, 1522-1522 (2020-08-28)
Nitrification is a key process for N-removal in engineered and natural environments, but recent findings of novel nitrifying microorganisms with surprising features revealed that our knowledge of this functional guild is still incomplete. Especially nitrite oxidation - the second step
Alexandre Lemire et al.
The Journal of organic chemistry, 70(6), 2368-2371 (2005-03-12)
[reaction: see text] A new methodology for the stereoselective synthesis of trans-2-substituted 3-amino-1,2,3,6-tetrahydropyridines is reported. The preparation of these 3-aminopiperidines is achieved by cycloaddition of nitrosobenzene with 2-substituted 1,2-dihydropyridines followed by chemoselective reduction of the cycloadducts. Enantioenriched 1,2-dihydropyridine derivatives are
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