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140864

Sigma-Aldrich

Mesitylene

reagent grade, 97%

Synonym(s):

1,3,5-Trimethylbenzene

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About This Item

Linear Formula:
C6H3(CH3)3
CAS Number:
108-67-8
Molecular Weight:
120.19
Beilstein:
906806
EC Number:
203-604-4
MDL number:
MFCD00008538
UNSPSC Code:
12352100
PubChem Substance ID:
329750394
NACRES:
NA.21

grade

reagent grade

Quality Level

200

vapor density

4.1 (vs air)

vapor pressure

14 mmHg ( 55 °C)
2.49 mmHg ( 25 °C)

Assay

97%

form

liquid

autoignition temp.

1022 °F

expl. lim.

0.88-6.1 %, 100 °F

refractive index

n20/D 1.499 (lit.)

bp

163-166 °C (lit.)

mp

−45 °C (lit.)

density

0.864 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(C)cc(C)c1

InChI

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

InChI key

AUHZEENZYGFFBQ-UHFFFAOYSA-N

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Application

  • Binders for metals in industrial processes: A study explored the use of hydroxyl-terminated dendrimers with sulfonimide linkers, where mesitylene was employed as a critical solvent in the synthesis process, offering potential in industrial metal binding applications (Abu Sbeih and Al Harahsheh, 2024).
  • Permeation networks for selective solvent filtration: Research demonstrated the use of mesitylene in creating superoleophilic, chemically and mechanically resistant percolation networks of ZIF-7 and ZIF-11 for the selective permeation of oils and chlorinated solvents, indicating its utility in industrial chemical processes (Prasanthi and Datta, 2023).
  • Green synthesis of covalent organic frameworks: A review highlighted the role of mesitylene in the green and facile preparation of covalent organic frameworks, emphasizing its significance in sustainable and advanced applications in chemical engineering (Azadi and Dinari, 2023).

Packaging

Packaged in glass bottles

replaced by

Product No.
Description
Pricing

M7200

Mesitylene, 98%

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

122.0 °F

Flash Point(C)

50 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Alessandro Scarso et al.
Journal of the American Chemical Society, 126(41), 13512-13518 (2004-10-14)
The reversible encapsulation of a series of normal alkane guests in a cylindrical host was studied by NMR methods. For small hydrocarbons such as n-pentane or n-hexane, two guests enter the host, and they move freely within. With n-heptane no
Soon Bang Kang et al.
The Journal of organic chemistry, 72(15), 5724-5730 (2007-06-28)
Facile synthesis of C-4 aryl pyrimidinone nucleoside analogues from an easily prepared O4-arylsulfonate derivative of thymidine is reported. Two O4-arylsulfonylthymidine precursors, (4-methylphenyl)sulfonyl and (2,4,6-trimethylphenyl)sulfonyl, were prepared and analyzed for their stabilities. Of the two, the latter possessed suitable stability as
Christoph Sprung et al.
Journal of the American Chemical Society, 137(5), 1916-1928 (2015-01-16)
A detailed and systematic polarized confocal fluorescence microscopy investigation is presented on three batches of large coffin-shaped ZSM-5 crystals (i.e., parent, steamed at 500 °C, and steamed at 700 °C). In total, six laser lines of different wavelength in the
Natalie D Coombs et al.
Dalton transactions (Cambridge, England : 2003), (3)(3), 332-337 (2008-04-17)
Sterically encumbered amido ligands based on a 1,8-diarylcarbazol-9-yl backbone have been investigated as electronically distinct alternatives to the widely-used terphenyl ligand class in the stabilization of low-coordinate metal complexes, and structurally characterized for the first time. While 1,8-diphenylcarbazol-9-yl derivatives are
Dalit Rechavi et al.
Journal of the American Chemical Society, 126(25), 7738-7739 (2004-06-24)
Isotope effects for the encapsulation of deuterated versus nondeuterated guests are determined. This system involves the use of social isomers, and the origin of the isotope effect is localized to methyl groups interacting with aromatic rings.
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