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140864

Sigma-Aldrich

Mesitylene

reagent grade, 97%

Synonyme(s) :

1,3,5-Trimethylbenzene

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About This Item

Formule linéaire :
C6H3(CH3)3
Numéro CAS:
Poids moléculaire :
120.19
Numéro Beilstein :
906806
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Qualité

reagent grade

Niveau de qualité

Densité de vapeur

4.1 (vs air)

Pression de vapeur

14 mmHg ( 55 °C)
2.49 mmHg ( 25 °C)

Pureté

97%

Forme

liquid

Température d'inflammation spontanée

1022 °F

Limite d'explosivité

0.88-6.1 %, 100 °F

Indice de réfraction

n20/D 1.499 (lit.)

Point d'ébullition

163-166 °C (lit.)

Pf

−45 °C (lit.)

Densité

0.864 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cc1cc(C)cc(C)c1

InChI

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

Clé InChI

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).

Conditionnement

Packaged in glass bottles

Remplacé(e)(s) par

Réf. du produit
Description
Tarif

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

122.0 °F

Point d'éclair (°C)

50 °C

Équipement de protection individuelle

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


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

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.
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.
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
Beata Janasik et al.
International archives of occupational and environmental health, 81(4), 443-449 (2007-08-08)
To investigate elimination of unchanged volatile organic compounds (VOC's) through urine and the use of respective data for occupational exposure assessment, six volunteers were exposed under controlled conditions to toluene (TOL), ethylbenzene (EB), xylene (XYL) and mesitylene (MES) at concentrations
Toshifumi Dohi et al.
Chemical communications (Cambridge, England), (40)(40), 4152-4154 (2007-10-11)
We have found that the use of fluoroalcohol media greatly enhanced the efficiency and scope of the direct dehydrative condensation of arenes and hypervalent iodine(III) compounds; the present clean method has a broad range of applicability as well as unique

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