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E44000

Sigma-Aldrich

2-Ethylphenol

99%

Sinónimos:

1-Ethyl-2-hydroxybenzene, 2-Ethylphenol, Phlorol, o-Ethylphenol, o-Hydroxyethylbenzene

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About This Item

Fórmula lineal:
C2H5C6H4OH
Número de CAS:
90-00-6
Peso molecular:
122.16
Beilstein/REAXYS Number:
1099397
EC Number:
201-958-4
MDL number:
MFCD00002249
UNSPSC Code:
12352100
PubChem Substance ID:
24894553
NACRES:
NA.22

assay

99%

refractive index

n20/D 1.536 (lit.)

bp

195-197 °C (lit.)

mp

−18 °C (lit.)

density

1.037 g/mL at 25 °C (lit.)

SMILES string

CCc1ccccc1O

InChI

1S/C8H10O/c1-2-7-5-3-4-6-8(7)9/h3-6,9H,2H2,1H3

InChI key

IXQGCWUGDFDQMF-UHFFFAOYSA-N

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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

172.4 °F - closed cup

flash_point_c

78 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Jan Lopatář et al.
Neuropharmacology, 93, 219-228 (2015-02-04)
The activation of Group I metabotropic glutamate receptors (GI mGluRs) in the hippocampus results in the appearance of persistent bursts of synchronised neuronal activity. In response to other stimuli, such activity is known to cause the release of the purines
Pasquale Filannino et al.
Applied and environmental microbiology, 80(24), 7574-7582 (2014-09-28)
The metabolism of hydroxycinnamic acids by strictly heterofermentative lactic acid bacteria (19 strains) was investigated as a potential alternative energy route. Lactobacillus curvatus PE5 was the most tolerant to hydroxycinnamic acids, followed by strains of Weissella spp., Lactobacillus brevis, Lactobacillus
T Schettgen et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 995-996, 93-100 (2015-06-06)
We have developed and validated a simple and sensitive method for the determination of urinary phenol as well as the urinary metabolites of toluene and ethylbenzene in one analytical run. After enzymatic hydrolysis for the cleavage of conjugates overnight, the
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following

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