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W322318

Sigma-Aldrich

Fenolo

≥99%

Sinonimo/i:

Idrossibenzene

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About This Item

Formula condensata:
C6H5OH
Numero CAS:
108-95-2
Peso molecolare:
94.11
Numero FEMA:
3223
Beilstein:
969616
Numero CE:
203-632-7
N° CoE:
11811
Numero MDL:
MFCD00002143
Codice UNSPSC:
12164502
ID PubChem:
24901564
Numero Flavis:
4.041
NACRES:
NA.21
Organolettico:
phenolic
Grado:
Halal
Kosher
Origine biologica:
synthetic
agenzia:
meets purity specifications of JECFA
Allergene alimentare:
no known allergens

Origine biologica

synthetic

Livello qualitativo

400

Grado

Halal
Kosher

agenzia

meets purity specifications of JECFA

Densità del vapore

3.24 (vs air)

Tensione di vapore

0.09 psi ( 55 °C)
0.36 mmHg ( 20 °C)

Saggio

≥99%

Stato

crystalline powder

Temp. autoaccensione

1319 °F

può contenere

≤0.15% hypophosphorous acid as additive

Limite di esplosione

8.6 %

P. ebollizione

182 °C (lit.)

Punto di fusione

40-42 °C (lit.)

Densità

1.071 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

phenolic

Stringa SMILE

Oc1ccccc1

InChI

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

Informazioni sul gene

human ... GABRA1(2554)

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Applicazioni


  • 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).

Esclusione di responsabilità

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

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

901590

Fenolo, 1.0 M in THF

901604

Fenolo, 1 M in dichloromethane

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Nervous system,Kidney,Liver,Skin

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

177.8 °F - closed cup

Punto d’infiammabilità (°C)

81 °C - closed cup

Dispositivi di protezione individuale

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
SHBQ0230
SHBQ1969
SHBQ1968
SHBP5219
SHBN4027

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Fenolo Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1047

Fenolo

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

Sigma-Aldrich

242322

Fenolo

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

Sigma-Aldrich

16017

Fenolo

Fenolo GR for analysis ACS,Reag. Ph Eur

Supelco

1.00206

Fenolo

Fenolo ≥89.0%

Sigma-Aldrich

P9346

Fenolo

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

Sigma-Aldrich

77607

Fenolo

Fenolo PESTANAL®, analytical standard

Supelco

35952

Fenolo

Fenolo United States Pharmacopeia (USP) Reference Standard

USP

1524806

Fenolo

Fenolo EMPROVE® ESSENTIAL, Ph. Eur., ChP, JP, USP

SAFC

1.00201

Fenolo

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
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
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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