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Merck
CN

8.05890

均三甲苯

Technipur®

别名:

1,3,5-三甲基苯

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线性分子式:
C6H3(CH3)3
化学文摘社编号:
108-67-8
分子量:
120.19
NACRES:
NA.22
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
906806
MDL number:
MFCD00008538
Grade:
synthesis grade
Bp:
163-166 °C (lit.)
Vapor pressure:
14 mmHg ( 55 °C)
2.49 mmHg ( 25 °C)
2.8 hPa ( 20 °C)

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产品名称

均三甲苯, Technipur®

SMILES string

Cc1cc(C)cc(C)c1

InChI key

AUHZEENZYGFFBQ-UHFFFAOYSA-N

InChI

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

grade

synthesis grade

vapor density

4.1 (vs air)

vapor pressure

14 mmHg ( 55 °C)
2.49 mmHg ( 25 °C)
2.8 hPa ( 20 °C)

autoignition temp.

1022 °F

expl. lim.

0.88-6.1 %, 100 °F

dilution

(for synthesis)

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.)

Quality Level

200

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Application

  • Mesitylene is used as a:
  • building block to manufacture antioxidants, plasticizers, rubber, adhesives, etc.
  • ligand in organometallic reactions
  • developer for photo patternable silicones
  • precursor to prepare a variety of fine chemicals

General description

Mesitylene is a methyl-substituted benzene hydrocarbon, a specialty solvent used for research and industrial applications. Derivatives of mesitylene are used as colorant precursors to prepare organic dye intermediates such as 2,4,6-trimethylaniline.

Legal Information

Technipur is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

122.0 °F

flash_point_c

50 °C

法规信息

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Comparative study of theoretical ultrasonic velocities of binary liquid mixtures containing quinoline and mesitylene at temperatures T = (303.15,308.15,313.15 and 318.15) K
Babavali SKF, et al.
Karbala International Journal of Modern Science, 1(3), 172-177 (2015)
Effect of catalyst morphology and hydrogen co-feeding on the acid-catalysed transformation of acetone into mesitylene
Quesada J, et al
Catalysis Science & Technology, 10, 1356-1367 (2020)
Nitro Compounds, Aromatic
Ullmann's Encyclopedia of Industrial Chemistry (2000)
Using Diamagnetic Yttrium and Lanthanum Complexes to Explore Ligand Reduction and C?H Bond Activation in a Tris(aryloxide)mesitylene Ligand System
Palumbo CT, et al.
Inorganic Chemistry, 57(20), 12876?12884-12876?12884 (2018)
Metal versus Ligand Reduction in Ln3+ Complexes of a Mesitylene-Anchored Tris(Aryloxide) Ligand
Palumbo CT, et al
Inorganic Chemistry, 57(5), 2823-2833 (2018)

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