Fenol solution

Name: Fenol solution
Brand: SUPELCO

certified reference material, 500 μg/mL in methanol

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Fórmula empírica (notación de Hill):

C₆H₆O

Número CAS:

108-95-2

Peso molecular:

94.11

UNSPSC Code:

12352200

PubChem Substance ID:

24872221

eCl@ss:

39023301

EC Number:

200-659-6

Beilstein/REAXYS Number:

6428463

MDL number:

MFCD00002143

NACRES:

NA.24

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Nombre del producto

Fenol solution, certified reference material, 500 μg/mL in methanol

InChI key

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

InChI

1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H

SMILES string

Oc1ccccc1

grade

certified reference material
TraceCERT^®

agency

EPA TO-8
NIOSH 2001
OSHA 32

product line

TraceCERT^®

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

500 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-30°C

Quality Level

300

Gene Information

human ... GABRA1(2554)

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Este artículo	16018	46344	PHR1047
Supelco 48688 Fenol solution	Sigma-Aldrich 16018 Fenol	Supelco 46344 Fenol solution	Supelco PHR1047 Fenol
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) -	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable
format single component solution	format -	format single component solution	format neat
Quality Level 300	Quality Level 200	Quality Level 100	Quality Level 300
grade certified reference material, TraceCERT^®	grade -	grade analytical standard	grade certified reference material, pharmaceutical secondary standard
storage temp. 2-30°C	storage temp. -	storage temp. 2-8°C	storage temp. 2-8°C
concentration 500 μg/mL in methanol	concentration -	concentration 100 μg/mL in acetonitrile	concentration -

Application

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

General description

Phenol can be obtained via a two-step process involving the oxidation of toluene by atmospheric oxygen, in the presence of cobalt catalyst to form benzoic acid as the major product, which is followed by the decarboxylation of benzoic acid in the presence of air and copper catalyst.[1] It mostly serves as an important chemical intermediate in the manufacture of synthetic organic materials.[2]

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.

Legal Information

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

pictograms

GHS02,GHS06,GHS08

signalword

Danger

hcodes

H225,H301 + H311 + H331,H370

pcodes

P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Phenolic Resins: Chemistry, Applications, Standardization, Safety and Ecology (2000)

Neff.M.J

Bioaccumulation in Marine Organisms: Effect of Contaminants from Oil Well Produced Water (2002)

Development of silicon-containing bis-phenol derivatives as androgen receptor antagonists: selectivity switching by C/Si exchange.

Masaharu Nakamura et al.

Bioorganic & medicinal chemistry, 21(7), 1643-1651 (2013-03-07)

We previously reported that bis-phenol derivatives, including LG190178 (3a), possess not only vitamin D receptor (VDR) agonistic activity, but also androgen receptor (AR) antagonistic activity. Here, we describe the design, synthesis and evaluation of silicon-containing bis-phenol derivatives, with the objective

Fpk1/2 kinases regulate cellular sphingoid long-chain base abundance and alter cellular resistance to LCB elevation or depletion.

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MicrobiologyOpen, 3(2), 196-212 (2014-02-11)

Sphingolipids are a family of eukaryotic lipids biosynthesized from sphingoid long-chain bases (LCBs). Sphingolipids are an essential class of lipids, as their depletion results in cell death. However, acute LCB supplementation is also toxic; thus, proper cellular LCB levels should

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Clinical cancer research : an official journal of the American Association for Cancer Research, 20(10), 2761-2772 (2014-03-25)

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Protocolos

GC Analysis of Phenols in Water

Analytical standard separation of various phenols for research and industrial applications.

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