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16017

Sigma-Aldrich

Phenol

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

Synonym(s):

Hydroxybenzene

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About This Item

Linear Formula:
C6H5OH
CAS Number:
Molecular Weight:
94.11
Beilstein:
969616
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.24 (vs air)

Quality Level

vapor pressure

0.09 psi ( 55 °C)
0.36 mmHg ( 20 °C)

grade

puriss.

Assay

99.5-100.5% (GC)

form

solid

autoignition temp.

1319 °F

quality

meets analytical specification of Ph. Eur., BP, USP

expl. lim.

8.6 %

impurities

acidic reac. Impurities, in accordance
organic volatile impurities, in accordance (GC)
≤0.05% non-volatile matter
≤0.3% water (Karl Fischer)

bp

182 °C (lit.)

mp

40-42 °C (lit.)

transition temp

solidification point ≥40 °C

density

1.071 g/mL at 25 °C (lit.)

suitability

in accordance for appearance of solution

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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General description

Phenol is an aromatic alcohol. Various industrial processes for the synthesis of phenol have been proposed.

Application

Phenol may be employed for the isolation of deoxyribonucleic acid from Bacillus subtilis. It may be used in the Berthelot color reaction for the quantitative estimation of ammonia.

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Description
Pricing

Signal Word

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

WGK

WGK 2

Flash Point(F)

177.8 °F

Flash Point(C)

81 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT.
H SAITO et al.
Biochimica et biophysica acta, 72, 619-629 (1963-08-20)
Tyman JHP.
Synthetic and Natural Phenols., 1-1 (1996)
Phenol-hypochlorite reaction for determination of ammonia.
Weatherburn M W.
Analytical Chemistry, 39(8), 971-974 (1967)
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
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

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