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Documenti fondamentali

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48549

Supelco

4-Nitrophenol

Sinonimo/i:

p-Nitrophenol

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About This Item

Formula condensata:
O2NC6H4OH
Numero CAS:
100-02-7
Peso molecolare:
139.11
Beilstein:
1281877
Numero CE:
202-811-7
Numero MDL:
MFCD00007331
Codice UNSPSC:
12000000
ID PubChem:
24872083

Grado

analytical standard

Tensione di vapore

0.6 mmHg ( 120 °C)

CdA

current certificate can be downloaded

Temp. autoaccensione

541 °F

Confezionamento

ampule of 5000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

279 °C (lit.)

Punto di fusione

110-115 °C (lit.)

Solubilità

H2O: soluble 15 g/L

applicazioni

environmental

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

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
BTJIUGUIPKRLHP-UHFFFAOYSA-N

Informazioni sul gene

human ... UGT1A4(54657)

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Applicazioni

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

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302 + H312 + H332,H373

Classi di pericolo

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

Organi bersaglio

Kidney,Liver

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

336.2 °F - closed cup

Punto d’infiammabilità (°C)

169.0 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
LRAD1441
LRAC4232
LRAB7599
LC26017V
LC24719V

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Fenolo unstabilized, ReagentPlus®, ≥99%

Sigma-Aldrich

185450

Fenolo

Acetaminophen Related Compound F Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1150

Acetaminophen Related Compound F

4-Nitrophenol sodium salt hydrate

Sigma-Aldrich

443662

4-Nitrophenol sodium salt hydrate

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
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
Siew Hong Lam et al.
Biochimica et biophysica acta, 1830(10), 4778-4789 (2013-06-25)
4-Nitrophenol (4-NP) is a prioritized environmental pollutant and its toxicity has been investigated using zebrafish, advocated as an alternative toxicological model. However, molecular information of 4-NP induced hepatotoxicity is still limited. This study aimed to obtain molecular insights into 4-NP-induced
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
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