Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

C61208

Sigma-Aldrich

2-Chloro-4-nitrophenol

97%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
ClC6H3(NO2)OH
CAS Number:
619-08-9
Molecular Weight:
173.55
EC Number:
210-578-8
MDL number:
MFCD00043910
UNSPSC Code:
12352100
PubChem Substance ID:
24892836
NACRES:
NA.22

Assay

97%

form

powder

mp

105-106 °C (lit.)

SMILES string

Oc1ccc(cc1Cl)[N+]([O-])=O

InChI

1S/C6H4ClNO3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H

InChI key

BOFRXDMCQRTGII-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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

Hassan Sakhtah et al.
Applied and environmental microbiology, 85(14) (2019-05-06)
The yeast Kluyveromyces lactis has been a successful host for the production of heterologous proteins for over 30 years. Currently, the galactose-/lactose-inducible and glucose-repressible LAC4 promoter (P
Tangrong Liu et al.
Analytical and bioanalytical chemistry, 411(7), 1467-1477 (2019-02-02)
α-L-Fucosidase (AFU) is a promising therapeutic target for the treatment of inflammation, cancer, cystic fibrosis, and fucosidosis. Some of the existing analytical methods for the assessment of AFU activity are lacking in sensitivity and selectivity, since most of them are
G I Konoshenko et al.
Antibiotiki, 27(9), 687-693 (1982-01-01)
When used in concentrations of 10-15 micrograms per 10(8) cells, flavofungin and nigrofungin, carbonyl-conjugated pentaenes lowered the rate of oxygen absorption by thymocyte suspensions in the presence of glucose. Flavopentin inhibited glucose oxidation in higher concentrations. ADP and succinate did
Y A Soushko et al.
Revue de laryngologie - otologie - rhinologie, 114(1), 59-61 (1993-01-01)
In vitro experiments, Terrilytinum* increases the antimycotic activity of Clotrimazolum* and Nitrofungin*, and cancels out the inhibitory effect of Contrycal*. The combined application of Clotrimazolum and Nitrofungin with Terrilytinum and Contrycal as treatment of otomycosis of the middle ear has
V G Arzumanyan et al.
Bulletin of experimental biology and medicine, 131(4), 346-349 (2001-09-11)
Viability of 40 Candida spp. cultures was studied after long-term exposure to antifungal drugs in minimum inhibitory concentrations. The fungicidal effect decreased in the series: pimafucin-nitrofungin-diflucan-orungal-levorine-clotrimazole-exoderil. Nizoral in a concentration of 4 microg/ml was ineffective; in the rest cultures the
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