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Merck

35836

4-Nitrophenol

PESTANAL®, analytical standard

Synonym(s):

p-Nitrophenol

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About This Item

Linear Formula:
O2NC6H4OH
CAS Number:
100-02-7
Molecular Weight:
139.11
NACRES:
NA.24
PubChem Substance ID:
329755228
eCl@ss:
39032018
UNSPSC Code:
41116107
EC Number:
202-811-7
MDL number:
MFCD00007331
Beilstein/REAXYS Number:
1281877

Product Name

4-Nitrophenol, PESTANAL®, analytical standard

InChI key

BTJIUGUIPKRLHP-UHFFFAOYSA-N

InChI

1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H

SMILES string

O=N(C1=CC=C(O)C=C1)=O

grade

analytical standard

vapor pressure

0.6 mmHg ( 120 °C)

product line

PESTANAL®

assay

100% (HPLC)

autoignition temp.

541 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

279 °C (lit.)

mp

110-115 °C (lit.)

application(s)

agriculture
environmental

format

neat

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - STOT RE 2 Oral

target_organs

Kidney,Liver

Storage Class

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

wgk

WGK 2

flash_point_f

336.2 °F - closed cup

flash_point_c

169.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9145
BCCL8712
BCCK5231
BCCH2129
BCCG6799

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Alex V Birk et al.
The Journal of laboratory and clinical medicine, 140(3), 166-175 (2002-09-25)
Extracellular adenosine triphosphate (ATP) regulates platelet reactivity by way of direct action on platelet purinergic receptors or by hydrolysis to adenosine diphosphate (ADP). Subsequent metabolism of ATP and ADP to adenosine monophosphate (AMP) and adenosine inhibits platelet aggregation. Endothelial cell
Ali Mehdinia et al.
Journal of chromatography. A, 1283, 82-88 (2013-03-08)
In this study, an analytical procedure for the selective extraction and detection of 4-nitrophenol (4-NP) was investigated by using of molecularly imprinted polymer on the surface of magnetic nanoparticles (MNPs). The magnetic nanoparticles were modified by tetraethyl orthosilicate (TEOS) and
Ipsita K Sen et al.
Carbohydrate polymers, 91(2), 518-528 (2012-11-06)
Gold nanoparticles were synthesized by reducing chloroauric acid with a glucan, isolated from an edible mushroom Pleurotus florida, cultivar Assam Florida. Here, glucan acts as reducing as well as stabilizing agent. The synthesized gold nanoparticles were characterized by UV-visible spectroscopy
Jau-Rung Chiou et al.
Journal of hazardous materials, 248-249, 394-400 (2013-02-19)
Silver/iron oxide composite nanoparticles have been synthesized successfully via a facile one-pot green route by the use of l-arginine, which created an aqueous solution of about pH 10 and acted as a reducing agent for the successive formation of iron
Simon De Corte et al.
Colloids and surfaces. B, Biointerfaces, 102, 898-904 (2012-10-31)
An increasing demand for catalytic Pd nanoparticles has motivated the search for sustainable production methods. An innovative approach uses bacterial cells as support material for synthesizing Pd nanoparticles by reduction of Pd(II) with e.g. hydrogen or formate. Nevertheless, drawbacks of
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