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PHR1150

Supelco

Acetaminophen Related Compound F

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

4-Nitrophenol, Paracetamol Impurity F, p-Nitrophenol

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About This Item

Linear Formula:
O2NC6H4OH
CAS Number:
Molecular Weight:
139.11
Beilstein:
1281877
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

Agency

traceable to USP 1003064

vapor pressure

0.6 mmHg ( 120 °C)

API family

acetaminophen, paracetamol

CofA

current certificate can be downloaded

autoignition temp.

541 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

279 °C (lit.)

mp

110-115 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

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

InChI

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

InChI key

BTJIUGUIPKRLHP-UHFFFAOYSA-N

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General description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Values of analytes vary lot to lot.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAA8987 in the slot below. This is an example certificate only and may not be the lot that you receive.

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Description
Pricing

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Kidney,Liver

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

336.2 °F

Flash Point(C)

169 °C


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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
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
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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