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E49606

Sigma-Aldrich

3-Ethyltoluene

99%

Synonym(s):

1-Ethyl-3-methylbenzene

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About This Item

Linear Formula:
C2H5C6H4CH3
CAS Number:
620-14-4
Molecular Weight:
120.19
Beilstein/REAXYS Number:
1850821
EC Number:
210-626-8
MDL number:
MFCD00009259
UNSPSC Code:
12352100
PubChem Substance ID:
24894592
NACRES:
NA.22

Quality Level

100

assay

99%

form

liquid

autoignition temp.

896 °F

refractive index

n20/D 1.496 (lit.)

bp

158-159 °C (lit.)

density

0.865 g/mL at 25 °C (lit.)

SMILES string

CCc1cccc(C)c1

InChI

1S/C9H12/c1-3-9-6-4-5-8(2)7-9/h4-7H,3H2,1-2H3

InChI key

ZLCSFXXPPANWQY-UHFFFAOYSA-N

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Application

3-Ethyltoluene is generally used as a model alkylbenzene derivative for bond activation and C(sp3)-H functionalization studies.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

wgk_germany

WGK 3

flash_point_f

100.4 °F

flash_point_c

38 °C

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A Metal?Free Oxidative Dehydrogenative Diels?Alder Reaction for Selective Functionalization of Alkylbenzenes.
Manna S and Antonchick A P
Chemistry?A European Journal, 23(32), 7825-7829 (2017)
Cu-Facilitated C? O Bond Formation Using N-Hydroxyphthalimide: Efficient and Selective Functionalization of Benzyl and Allylic C? H Bonds.
Lee J M, et al.
Journal of the American Chemical Society, 130(25), 7824-7825 (2008)
Mechanism of C? H Bond Activation of Alkyl-Substituted Benzenes by Cationic Platinum (II) Complexes.
Driver T G, et al.
Organometallics, 24(15), 3644-3654 (2005)
Laura Vallecillos et al.
The Science of the total environment, 666, 235-244 (2019-02-25)
This study describes the implementation of a passive sampling-based method followed by thermal desorption gas-chromatography-mass spectrometry (TD-GC-MS) for the monitoring of volatile organic compounds (VOCs) in industrial atmospheres. However, in order to employ passive sampling as a reliable sampling technique
G M Whited et al.
Journal of bacteriology, 166(3), 1028-1039 (1986-06-01)
Pseudomonas putida BG1 was isolated from soil by enrichment with p-toluate and selection for growth with p-xylene. Other hydrocarbons that served as growth substrates were toluene, m-xylene, 3-ethyltoluene, and 1,2,4-trimethylbenzene. The enzymes responsible for growth on these substrates are encoded
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