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| Product Name: | Mesitylene | | Synonyms: | Mesitylene reagent grade, 97%;Mcsitylene(1,3,5-Trimethy1benzenc);1,3,5-trimethyl-benzen;1,3,5-trimethylbenzene(1,3,5-tmb);3,5-dimethyltoluene;Benzene,1,3,5-trimethyl-;I,3,5-TrimethylbenzolG%305;1,3,5-trimethylbenzene solution | | CAS: | 108-67-8 | | MF: | C9H12 | | MW: | 120.19 | | EINECS: | 203-604-4 | | Product Categories: | Arenes;Building Blocks;Chemical Synthesis;Organic Building Blocks;Benzene derivates;Analytical Chemistry;Standard Solution of Volatile Organic Compounds for Water & Soil Analysis;Standard Solutions (VOC);K00001 | | Mol File: | 108-67-8.mol |  |
| | Mesitylene Chemical Properties |
| Melting point | -45 °C | | Boiling point | 163-166 °C(lit.) | | density | 0.864 g/mL at 25 °C(lit.) | | vapor density | 4.1 (vs air) | | vapor pressure | 14 mm Hg ( 55 °C) | | refractive index | n20/D 1.499(lit.) | | Fp | 112 °F | | storage temp. | 2-8°C | | solubility | Miscible with alcohol, benzene, ether (Windholz et al., 1983), and trimethylbenzene isomers. | | form | Liquid | | pka | >14 (Schwarzenbach et al., 1993) | | color | Clear colorless | | explosive limit | 0.88-6.1%, 100°F | | Odor Threshold | 0.17ppm | | Water Solubility | 2.9 g/L (20 ºC) | | Merck | 14,5907 | | BRN | 906806 | | Henry's Law Constant | 4.03, 4.60, 5.71, 6.73, and 9.63 at 10, 15, 20, 25, and 30 °C, respectively (EPICS, Ashworth et al.,1988) | | Exposure limits | NIOSH REL: TWA 25 ppm (125 mg/m3); ACGIH TLV: TWA for mixed
isomers 25 ppm (adopted). | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents. | | InChIKey | AUHZEENZYGFFBQ-UHFFFAOYSA-N | | LogP | 3.42 at 20℃ | | CAS DataBase Reference | 108-67-8(CAS DataBase Reference) | | NIST Chemistry Reference | Benzene, 1,3,5-trimethyl-(108-67-8) | | EPA Substance Registry System | 1,3,5-Trimethylbenzene (108-67-8) |
| | Mesitylene Usage And Synthesis |
| Outline | The molecular structure of mesitylene (also known as mesitylene, molecular formula is C9H12) is σ bond which formed by benzene ring C atoms by means of sp2 hybrid orbital, other C atoms form σ bond by means of sp3 hybrid orbital, it is functional group in the presence of many multi organic compounds. It is aromatic hydrocarbon which obtained by three hydrogens symmetrically-substituted by three methyl in benzene ring.It is widespread in coal tar and certain petroleum. It is colorless liquid, toxic, flammable and explosive. The freezing point is-44.72 ℃, melting point is-44.7 ℃, boiling point is 164.7 ℃, the relative density is 0.8652 (20/4℃). Mesitylene can generate trimesic acid with the oxidation of dilute nitric acid. Pure mesitylene is made by acetone in vapor phase catalytic dehydrationthe at 300~500℃.
Mesitylene is important organic chemical raw material, the use of mesitylene can develop three toluene, trimesic acid, benzoic anhydride and other dye intermediates, it can also be used for the production of antioxidants, polyester resin curing agent, stabilizer, alkyd resins and plasticizers. Since mesitylene is a good solvent, and it is flammable, irritant, and it has low freezing point. In the electronics industry, it is used as developer of photosensitive sheet silicone.
Mesitylene is also common volatile organic compound (VOC) in city, this is mainly generated by the combustion. It plays an important role (including aerosol and tropospheric ozone generation) in many chemical reactions in the atmosphere. Since the three hydrogens on the aromatic ring have the same chemical environment, in the mesitylene magnetic resonance spectrum hydrogen spectrum only has a single peak which peak area is corresponding to three hydrogen in the vicinity of 6.8ppm. Therefore, mesitylene is sometimes used as internal standard substance in proton nuclear magnetic resonance method which comprises aromatic organic samples.
The annual demand of mesitylene is about 100,000 tons in current domestic market.
The above information is edited by the chemicalbook of Wang Xiaodong.
| | Chemical Properties | It is colorless transparent liquid. It is insoluble in water, soluble in ethanol, it can dissolve in benzene, ether, acetone in any proportion.
| | Uses | It can be used for the production of trimesic acid and antioxidants, epoxy curing agents, stabilizers polyester resin, alkyd resin, plasticizers and dyes etc.
It can be used as raw material of organic synthesis, it can be used in the preparation of trimesic acid, and antioxidants, epoxy curing agents, stabilizers polyester resin, alkyd resin, plasticizer, 2,4,6-trimethyl aniline reactive brilliant blue, K-3R and other dye.
It can be used as analytical reagents, solvents, it can be also used in organic synthesis, etc.
| | Production method | 1. It is derived by the separation of C9 aromatic hydrocarbon. 2. In the reforming of heavy aromatics the amount of mesitylene is about 11.8%. However, due to its boiling point (164.7 ℃) is extremely close to the boiling point of O-methyl benzene (165.15 ℃), it is difficult to separate for using distillation method. 3.The isomerization method with partial three toluene as raw material can fractionate, and can get mesitylene which the one way yield is 21.6%, the purity is more than 95%, while 4%-7% of by-product is durene, xylene is 9%. The average temperature of reactor bed is 260℃, pressure is 2.35MPa, empty the entire is 1.0h-1, molar ratio of reforming hydrogen and oil is 10: 1, the catalyst is mordenite which lack of aluminum hydrogen form: Cu: Ni: binder = 85.2: 0.5: 15. Under these conditions, the conversion rate of partial three toluene is 46%, selectivity is 47% , one way yield of mesitylene is 21.6%. HF-BF3 is xylene separated and through the method of isomerization by Japanese Mitsubishi Gas Company, by-products contain high concentration of mesitylene of high boiling, the goods can be get by distilled and refined. 4. Acetone in sulfuric acid-catalyzed goes through dehydration synthesis can obtain this goods with the yield of 13%-15%. 4600g (79mol) of industrial acetone is cooled to 0-5℃, and 4160ml concentrated sulfuric acid is added with stirring, the temperature can not exceed 10℃. After addition is completed, cntinue stirring 3-4h, place at room temperature for 18-24h. The product is subjected to steam distillation, mesitylene is separated, then it is washed with alkali, water, and then collect distillation fraction of 210℃, 15g sodium metal is added into this fraction, it is heated to near the boiling point, 2/3 liquid is evaporated. the residue is distilled to 210℃, efficient fractionation collection is done for the 163-167℃ distillate, 430-470g1,3,5-mesitylene can be obtained.
| | Category | It is flammable liquid.
| | Toxicity grading | Low toxicity.
| | Acute toxicity | Inhalation-rat LC50: 24000 mg/m/4 hours. | | Stimulus data | Skin-Rabbit 20 mg/24 hours of moderate; Eyes-rabbit 500 mg/24 hr mild. | | Flammability hazard characteristics | It is inflammable in case of fire, heat, oxidants; when burning stimulated smoke can generate.
| | Storage characteristics | Treasury should have ventilation and be low-temperature drying; and it should stored separately with oxidants.
| | Extinguishing agent | Dry powder, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent.
| | Professional standards | TWA 120 mg/m³; STEL 170 mg/m. | | Chemical Properties | colourless liquid with an aromatic odour | | Chemical Properties | Mesitylene is a clear, colorless liquid.
Distinctive, aromatic odor. | | Physical properties | Colorless liquid with a peculiar odor. An odor threshold concentration of 170 ppbv was reported
by Nagata and Takeuchi (1990). | | Uses | Intermediate, including anthraquinone vat dyes,
UV oxidation stabilizers for plastics. | | Uses | Mesitylene is used to make plastics and dyes. It acts as a solvent, ligand in organometallic chemistry and precursor to 2,4,6-trimethylaniline. It is also used as a developer for photopatternable silicones due to its solvent properties in the electronics industry. It is used as an internal standard in nuclear magnetic resonance (NMR) samples due to the presence of three equivalent protons in it. It is involved in the production of trimesic acid and antioxygen, epoxy firming agent and polyester resin stabilizers. Further, it is used as an additive and component in aviation gasoline blends. | | Definition | ChEBI: A trimethylbenzene carrying methyl substituents at positions 1, 3 and 5. | | Synthesis Reference(s) | Journal of the American Chemical Society, 92, p. 3232, 1970 DOI: 10.1021/ja00713a078
The Journal of Organic Chemistry, 19, p. 923, 1954 DOI: 10.1021/jo01371a008 | | General Description | A colorless liquid with a peculiar odor. Insoluble in water and less dense than water. Flash point near 123°F. May be toxic by ingestion and inhalation. Used to make plastics and dyes. | | Air & Water Reactions | Flammable. Insoluble in water. | | Reactivity Profile | TRIMETHYLBENZENE is incompatible with the following: Oxidizers, nitric acid . | | Hazard | Moderate fire hazard. Toxic by inhalation.
Central nervous system impairment, asthma, and
hematologic effects. | | Health Hazard | May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. | | Fire Hazard | HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. | | Safety Profile | Poison by inhalation.
Moderately toxic by intraperitoneal route.
Human systemic effects by inhalation:
sensory changes involving peripheral nerves,
somnolence (general depressed activity), and
structural or functional change in trachea or
bronchi. Reports of leukopenia and
thrombocytopenia in experimental animals.
A mild skin and eye irritant. A flammable
liquid when exposed to heat or flame; can
react vigorously with oxidizing materials.
Violent reaction with HNO3. To fight fire,
use water spray, fog, foam, CO2. Emitted
from modern buildmg materials (CENEAR
69,22,91). When heated to decomposition it
emits acrid smoke and irritating fumes. | | Potential Exposure | Mesitylene is used as raw material in
chemical synthesis and as ultraviolet stabilizer; as a paint
thinner, solvent, and motor fuel component; as an intermediate in organic chemical manufacture. | | Source | Detected in distilled water-soluble fractions of 87 octane gasoline (0.34 mg/L), 94 octane
gasoline (1.29 mg/L), Gasohol (0.48 mg/L), No. 2 fuel oil (0.08 mg/L), jet fuel A (0.09 mg/L),
diesel fuel (0.03 mg/L), and military jet fuel JP-4 (0.09 mg/L) (Potter, 1996). Schauer et al. (1999)
reported 1,3,5-trimethylbenzene in a diesel-powered medium-duty truck exhaust at an emission
rate of 260 μg/km.
California Phase II reformulated gasoline contained 1,3,5-trimethylbenzene at a concentration of
7.45 g/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without
catalytic converters were 1.98 and 210 mg/km, respectively (Schauer et al., 2002).
Thomas and Delfino (1991) equilibrated contaminant-free groundwater collected from
Gainesville, FL with individual fractions of three individual petroleum products at 24–25 °C for
24 h. The aqueous phase was analyzed for organic compounds via U.S. EPA approved test method
602. Average 1,3,5-trimethylbenzene concentrations reported in water-soluble fractions of
unleaded gasoline, kerosene, and diesel fuel were 333, 86, and 13 μg/L, respectively. When the
authors analyzed the aqueous-phase via U.S. EPA approved test method 610, average 1,3,5-
trimethylbenzene concentrations in water-soluble fractions of unleaded gasoline, kerosene, and
diesel fuel were greater, i.e., 441, 91, and 27 μg/L, respectively.
Drinking water standard: No MCLGs or MCLs have been proposed (U.S. EPA, 2000). | | Environmental fate | Biological. In anoxic groundwater near Bemidji, MI, 1,3,5-trimethylbenzene anaerobically
biodegraded to the intermediate tentatively identified as 3,5-dimethylbenzoic acid (Cozzarelli et
al., 1990).
Photolytic. Glyoxal, methylglyoxal, and biacetyl were produced from the photooxidation of
1,3,5-trimethylbenzene by OH radicals in air at 25 °C (Tuazon et al., 1986a). The rate constant for
the reaction of 1,3,5-trimethylbenzene and OH radicals at room temperature was 4.72 x 10-11
cm3/molecule?sec (Hansen et al., 1975). A rate constant of 2.97 x 10-8 L/molecule?sec was reported
for the reaction of 1,3,5-trimethylbenzene with OH radicals in the gas phase (Darnall et al., 1976).
Similarly, a room temperature rate constant of 6.05 x 10-11 cm3/molecule?sec was reported for the
vapor-phase reaction of 1,3,5-trimethylbenzene with OH radicals (Atkinson, 1985). At 25 °C, a
rate constant of 3.87 x 10-11 cm3/molecule?sec was reported for the same reaction (Ohta and
Ohyama, 1985).
Chemical/Physical. 1,3,5-Trimethylbenzene will not hydrolyze because it does not contain a
hydrolyzable functional group (Kollig, 1993). | | Shipping | UN1993 Flammable liquids, n.o.s., Hazard Class:
3; Labels: 3-Flammable liquid, Technical Name Required.
| | Purification Methods | Dry it with CaCl2 and distil it from Na in a glass helices-packed column. Treat it with silica gel and redistil it. Alternative purifications include vapour-phase chromatography, or fractional distillation followed by azeotropic distillation with 2-methoxyethanol (which is subsequently washed out with H2O), drying and fractional distilling. More exhaustive purification uses sulfonation by dissolving in two volumes of conc H2SO4, precipitating with four volumes of conc HCl at 0o, washing with conc HCl and recrystallising from CHCl3. The mesitylene sulfonic acid is hydrolysed with boiling 20% HCl and steam distilled. The separated mesitylene is dried (MgSO4 or CaSO4) and distilled. It can also be fractionally crystallised from the melt at low temperatures. [Beilstein 5 IV 1016.] | | Incompatibilities | Vapors forms explosive mixture with air.
Violent reaction with nitric acid. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause
fires or explosions. Keep away from alkaline materials,
strong bases, strong acids, oxoacids, epoxides | | Waste Disposal | Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal,
state, and local environmental regulations must be
observed. |
| | Mesitylene Preparation Products And Raw materials |
| Raw materials | Sodium-->PROPYLENE-->Ethylbenzene-->DOYLE DIRHODIUM CATALYST-RH2(4S-MEOX)4-->2-Amino-3-chlorobenzoic acid-->1,2,4-Trimethylbenzene-->1,2,4,5-Tetramethylbenzene-->Heavy aromatics | | Preparation Products | p-Anisaldehyde-->3-Hydroxybenzoic acid-->O-Mesitylenesulfonylhydroxylamine-->MESITYLACETIC ACID-->2,4,6-Trimethylaniline-->Levodopa-->Mesitylene-2-sulfonyl chloride-->Reactive Blue 74-->3,5-Dimethylbenzoic acid-->VANILLA EXTRACT-->2,4-MESITYLENEDISULFONYL DICHLORIDE-->Mesitaldehyde-->2,4,6-Trimethybromombenzene-->Trimesic acid-->2-NITROMESITYLENE-->2,4,6-Trimethylbenzoic acid-->3,3',5,5'-TETRAMETHYLBIBENZYL-->3,5-Dimethylbenzaldehyde |
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