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Merck

48688

Phénol solution

certified reference material, 500 μg/mL in methanol

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A propos de cet article

Formule empirique (notation de Hill) :
C6H6O
Numéro CAS:
108-95-2
Poids moléculaire :
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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Nom du produit

Phénol 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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Catégories apparentées

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. It mostly serves as an important chemical intermediate in the manufacture of synthetic organic materials.

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

signalword

Danger

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

Classe de stockage

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Neff.M.J
Bioaccumulation in Marine Organisms: Effect of Contaminants from Oil Well Produced Water (2002)
Gardziella.A, et al.
Phenolic Resins: Chemistry, Applications, Standardization, Safety and Ecology (2000)
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
Mark J Lee et al.
PLoS pathogens, 11(10), e1005187-e1005187 (2015-10-23)
Of the over 250 Aspergillus species, Aspergillus fumigatus accounts for up to 80% of invasive human infections. A. fumigatus produces galactosaminogalactan (GAG), an exopolysaccharide composed of galactose and N-acetyl-galactosamine (GalNAc) that mediates adherence and is required for full virulence. Less
Yukari Yamane-Sando et al.
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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