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40063

Supelco

Phénol solution

5000 μg/mL in methanol, certified reference material

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About This Item

Formule empirique (notation de Hill):
C6H6O
Numéro CAS:
108-95-2
Poids moléculaire :
94.11
Numéro Beilstein :
6428463
Numéro MDL:
MFCD00002143
Code UNSPSC :
41116105
ID de substance PubChem :
24864936

Qualité

certified reference material
TraceCERT®

Niveau de qualité

300

Agence

EPA TO-8
NIOSH 2001
OSHA 32

Gamme de produits

TraceCERT®

CofA (certificat d'analyse)

current certificate can be downloaded

Caractéristiques

standard type calibration

Conditionnement

ampule of 1 mL

Concentration

5000 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

Température de stockage

2-8°C

Chaîne SMILES 

Oc1ccccc1

InChI

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

Clé InChI

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Informations sur le gène

human ... GABRA1(2554)

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Catégories apparentées

Description générale

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Application

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

Autres remarques

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.

Informations légales

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

Pictogrammes

FlameSkull and crossbonesHealth hazard
GHS02,GHS06,GHS08

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Eyes,Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

49.5 °F - closed cup

Point d'éclair (°C)

9.7 °C - closed cup

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
LRAD5364
LRAD1538
LRAC4235
LRAB8628
XA23448V

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

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Les clients ont également consulté

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Phénol solution ≥89.0%

Sigma-Aldrich

P9346

Phénol solution

Phénol solution for synthesis

Sigma-Aldrich

8.43984

Phénol solution

Phénol GR for analysis ACS,Reag. Ph Eur

Supelco

1.00206

Phénol

Serdar Durdagi et al.
Bioorganic & medicinal chemistry, 19(4), 1381-1389 (2011-02-02)
Carbonic anhydrases (CAs, EC 4.2.1.1) are inhibited by sulfonamides, inorganic anions, phenols, coumarins (acting as prodrugs) and polyamines. A novel class of CA inhibitors (CAIs), interacting with the CA isozymes I, II (cytosolic) and IX, XII (transmembrane, tumor-associated) in a
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
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
Rita A Busuttil et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 20(10), 2761-2772 (2014-03-25)
Gene-expression profiling has revolutionized the way we think about cancer and confers the ability to observe the synchronous expression of thousands of genes. The use of putative genome-level expression profiles has allowed biologists to observe the complex interactions of genes
Kyoko Matsumoto et al.
Nucleic acids research, 42(16), e125-e125 (2014-07-19)
To identify and characterize transcript structures ranging from transcriptional start sites (TSSs) to poly(A)-addition sites (PASs), we constructed and analyzed human TSS/PAS mate pair full-length cDNA libraries from 14 tissue types and four cell lines. The collected information enabled us
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