All Photos(4)

N24609

Sigma-Aldrich

Nitrosobenzene

greener alternative

≥97%

Synonym(s):
NOB
Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
Molecular Weight:
107.11
Beilstein:
605688
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥97%

form

solid

greener alternative product score

old score: 8
new score: 5
Find out more about DOZN™ Scoring

greener alternative product characteristics

Waste Prevention
Atom Economy
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

bp

59 °C/18 mmHg (lit.)

mp

65-69 °C (lit.)

greener alternative category

Re-engineered

storage temp.

2-8°C

SMILES string

O=Nc1ccccc1

InChI

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

InChI key

NLRKCXQQSUWLCH-UHFFFAOYSA-N

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Application

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

Packaging

10, 25 g in glass bottle

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Certificate of Origin

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
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
Xiuzhen Shi et al.
Environmental microbiology, 19(12), 4851-4865 (2017-07-29)
Soil ecosystem represents the largest contributor to global nitrous oxide (N
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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