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Documentos

W322318

Sigma-Aldrich

Fenol

≥99%

Sinónimos:

Hidroxibenceno

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About This Item

Fórmula lineal:
C6H5OH
Número de CAS:
108-95-2
Peso molecular:
94.11
FEMA Number:
3223
Beilstein/REAXYS Number:
969616
EC Number:
203-632-7
Council of Europe no.:
11811
MDL number:
MFCD00002143
UNSPSC Code:
12164502
PubChem Substance ID:
24901564
Flavis number:
4.041
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

Halal
Kosher

agency

meets purity specifications of JECFA

vapor density

3.24 (vs air)

vapor pressure

0.09 psi ( 55 °C)
0.36 mmHg ( 20 °C)

assay

≥99%

form

crystalline powder

autoignition temp.

1319 °F

may contain

≤0.15% hypophosphorous acid as additive

expl. lim.

8.6 %

bp

182 °C (lit.)

mp

40-42 °C (lit.)

density

1.071 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

phenolic

SMILES string

Oc1ccccc1

InChI

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

InChI key

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

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Categorías relacionadas

Application


  • Revealing mechanism of phenolic-amine reaction to form humus in compost based on high-resolution liquid chromatography mass spectrometry and spectroscopy.: This study delves into the complex reactions between phenolic compounds and amines during compost formation, shedding light on the molecular pathways that lead to humus production, crucial for soil fertility and carbon sequestration (Zhou et al., 2024).

  • Unlocking the potential of phenolated kraft lignin as a versatile feed additive.: This paper explores the utilization of phenolated kraft lignin as a feed additive, examining its benefits in animal nutrition and its role in sustainable agricultural practices (Li et al., 2024).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

related product

Referencia del producto
Descripción
Precios

901590

Fenol solution, 1.0 M in THF

901604

Fenol solution, 1 M in dichloromethane

signalword

Danger

Hazard Classifications

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

target_organs

Nervous system,Kidney,Liver,Skin

Storage Class

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

wgk_germany

WGK 2

flash_point_f

177.8 °F - closed cup

flash_point_c

81 °C - closed cup

ppe

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

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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Fenol contains hypophosphorous as stabilizer, loose crystals, ACS reagent, ≥99.0%

Sigma-Aldrich

242322

Fenol

Fenol puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)

Sigma-Aldrich

16017

Fenol

Fenol solution ≥89.0%

Sigma-Aldrich

P9346

Fenol solution

Fenol BioUltra, for molecular biology, TE-saturated, ~73% (T)

Sigma-Aldrich

77607

Fenol

Fenol PESTANAL®, analytical standard

Supelco

35952

Fenol

Fenol United States Pharmacopeia (USP) Reference Standard

USP

1524806

Fenol

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
Thitiporn Anunthawan et al.
Biochimica et biophysica acta, 1848(6), 1352-1358 (2015-03-15)
We investigated the mechanisms of two tryptophan-rich antibacterial peptides (KT2 and RT2) obtained in a previous optimization screen for increased killing of both Gram-negative and Gram-positive bacteria pathogens. At their minimal inhibitory concentrations (MICs), these peptides completely killed cells of
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
Saori Tomita et al.
Nature communications, 6, 6966-6966 (2015-04-30)
Estrogen receptor-α (ER)-positive breast cancer cells undergo hormone-independent proliferation after deprivation of oestrogen, leading to endocrine therapy resistance. Up-regulation of the ER gene (ESR1) is critical for this process, but the underlying mechanisms remain unclear. Here we show that the
Souhaila Bouatra et al.
PloS one, 8(9), e73076-e73076 (2013-09-12)
Urine has long been a "favored" biofluid among metabolomics researchers. It is sterile, easy-to-obtain in large volumes, largely free from interfering proteins or lipids and chemically complex. However, this chemical complexity has also made urine a particularly difficult substrate to
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