Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

N24609

Sigma-Aldrich

Nitrosobenzene

greener alternative

≥97%

Synonym(s):

NOB

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
586-96-9
Molecular Weight:
107.11
Beilstein:
605688
EC Number:
209-591-1
MDL number:
MFCD00002059
UNSPSC Code:
12352100
PubChem Substance ID:
24897573
NACRES:
NA.22

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

SMILES string

O=Nc1ccccc1

InChI

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

InChI key

NLRKCXQQSUWLCH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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.

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.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H312 + H332

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service