140864
Mesitylene
reagent grade, 97%
Synonym(s):
1,3,5-Trimethylbenzene
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About This Item
Linear Formula:
C6H3(CH3)3
CAS Number:
Molecular Weight:
120.19
Beilstein:
906806
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
grade
reagent grade
Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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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
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.
Sanyog Sharma et al.
Organic & biomolecular chemistry, 11(4), 654-661 (2012-12-12)
Two mesitylene based probes, having catechol/phenol units in conjunction to the Schiff base have been synthesized. The probe with a catechol unit can be used to sense and discriminate between F(-) and CN(-) through different colorimetric and fluorimetric responses using
Jacqueline M Veauthier et al.
Inorganic chemistry, 43(4), 1220-1228 (2004-02-18)
New bimetallic mu-oxo diferric complexes of several previously reported calix[4]pyrrole Schiff base macrocycles are described. The synthesis of a new member of this class of macrocycles is also reported; it was prepared via an acid-catalyzed condensation between 1,9-bisformyl-5,5-dipropyldipyrromethane and o-phenylenediamine.
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
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