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Key Documents

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35952

Supelco

Fenol

PESTANAL®, analytical standard

Sinónimos:

Hidroxibenceno

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About This Item

Fórmula lineal:
C6H5OH
Número de CAS:
108-95-2
Peso molecular:
94.11
Beilstein:
969616
Número CE:
203-632-7
Número MDL:
MFCD00002143
Código UNSPSC:
12352104
ID de la sustancia en PubChem:
329755237
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

densidad de vapor

3.24 (vs air)

presión de vapor

0.09 psi ( 55 °C)
0.36 mmHg ( 20 °C)

Línea del producto

PESTANAL®

temp. de autoignición

1319 °F

caducidad

limited shelf life, expiry date on the label

lim. expl.

8.6 %

técnicas

HPLC: suitable
gas chromatography (GC): suitable

bp

182 °C (lit.)

mp

40-42 °C (lit.)

densidad

1.071 g/mL at 25 °C (lit.)

aplicaciones

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

formato

neat

cadena SMILES

Oc1ccccc1

InChI

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

Clave InChI

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

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Descripción general

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

Aplicación

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

Productos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Información legal

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

Producto relacionado

Referencia del producto
Descripción
Precios

901590

Fenol solution, 1.0 M in THF

901604

Fenol solution, 1 M in dichloromethane

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - STOT RE 2

Órganos de actuación

Nervous system,Kidney,Liver,Skin

Código de clase de almacenamiento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

177.8 °F - closed cup

Punto de inflamabilidad (°C)

81 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
BCCG0109
BCCB8537
BCBW5491
BCBS3637V
SZBD127XV

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Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

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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
Britta T Eklund et al.
Marine pollution bulletin, 46(2), 171-181 (2003-02-15)
Toxic effects on macroalgae have been compiled. Eighty-two articles have been found in literature during 1959-2000. A total of 120 substances were investigated using 65 different macroalgae species. About one-third of the tested compounds were organic substances (33%), another third
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
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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