CAS 98-83-9
:α-Methylstyrene
Description:
α-Methylstyrene is an organic compound characterized by its aromatic structure, featuring a vinyl group attached to a methyl-substituted benzene ring. It is a colorless to pale yellow liquid with a sweet, floral odor. The compound is known for its low solubility in water but is soluble in organic solvents such as ethanol and ether. α-Methylstyrene has a relatively low boiling point and a moderate density compared to water. It is primarily used as a monomer in the production of various polymers and copolymers, particularly in the manufacturing of plastics and resins. Additionally, it serves as an intermediate in the synthesis of other chemical compounds. The substance is flammable and should be handled with care, as it can pose health risks upon inhalation or skin contact. Its reactivity includes participation in polymerization reactions, making it valuable in industrial applications. Proper safety measures should be observed when working with α-Methylstyrene to mitigate potential hazards.
Formula:C9H10
InChI:InChI=1S/C9H10/c1-8(2)9-6-4-3-5-7-9/h3-7H,1H2,2H3
InChI key:InChIKey=XYLMUPLGERFSHI-UHFFFAOYSA-N
SMILES:C(C)(=C)C1=CC=CC=C1
Synonyms:- (1-Methylethenyl)benzene
- 1-Methyl-1-phenylethene
- 1-Methyl-1-phenylethylene
- 1-Methylvinyl benzene
- 1-Phenyl-1-methylethylene
- 1-Propene, 2-phenyl-
- 2-Fenilpropeno
- 2-Phenyl Propene
- 2-Phenyl-1-Propene
- 2-Phenyl-1-propylene
- 2-Phenyl-2-propene
- 2-Phenyl-propylene
- 2-Phenylpropen
- 2-Phenylpropene
- 2-Phenylpropylene
- Benzene, (1-methylethenyl)-
- Benzene, isopropenyl-
- Dow Corning 56
- Isopropenyl Benzene
- Isopropenylbenzene
- K 150 (styrene)
- Methylstyrene
- Nsc 9400
- Prop-1-en-2-ylbenzene
- Styrene, α-methyl-
- alpha-Methylstyrene monomer
- α-METHYL STYRENE
- α-Methylstyrene
- α-Methylstyrol
- α-Methylvinylbenzene
- See more synonyms
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Found 10 products.
α-Methylstyrene (stabilized with TBC)
CAS:Formula:C9H10Purity:>99.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:118.18α-Methylstyrene, 99%, stab. with 10-20 ppm 4-tert-butylcatechol
CAS:<p>-Methylstyrene (AMS) is used in the synthesis of (acrylonitrile-styrene-acrylic copolymer)/(-methylstyrene-acrylonitrile copolymer). It is used in the manufacture of plasticizers, resins and polymers. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfo</p>Formula:C9H10Purity:99%Color and Shape:Clear, colorless, LiquidMolecular weight:118.18α-Methylstyrene
CAS:α-MethylstyreneFormula:C9H10Purity:≥95%Color and Shape: clear. almost colourless liquidMolecular weight:118.178g/molASTM Method D7845 Check Standard 0.01-0.05 Wt% in Toluene
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Color and Shape:Mixtureα-Methylstyrene
CAS:<p>Applications α-methylstyrene (AMS) is a useful intermediate. It can be used in the manufacture of plasticizers, resins and polymerization production processes. It is a co-product formed in a variation of the cumene process. The homopolymer obtained from this monomer, poly(α-methylstyrene), is unstable, being characterized by a low ceiling temperature.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lund, A., et al.: Spectrochim. Acta A, 98, 367 (2012); Natl. Toxicol. Program tech. report series, (543), 1-210 (2007); Chen, L., et al: Drug Metab. Dispos., 39, 498 (2011)<br></p>Formula:C9H10Color and Shape:ColourlessMolecular weight:118.18(1-Methylethenyl)-benzene contains 15 ppm p-tert-butylcatechol as inhibitor
CAS:Formula:C9H10Purity:95.0%Color and Shape:LiquidMolecular weight:118.1792-Phenyl-1-propene - stabilized with TBC
CAS:<p>2-Phenyl-1-propene stabilized with TBC is a monomer that is used in the production of cationic polymers. This polymer undergoes a free radical polymerization process, which requires a catalyst to initiate the reaction. The most commonly used catalyst for this process is an organometallic compound, such as titanium tetrachloride (TTC) or zirconium tetrachloride (ZTC). The kinetic data of this reaction show that the monomer reacts with two equivalents of TTC or ZTC. The reaction mechanism involves an initial addition reaction between TTC/ZTC and the hydroxyl group on 2-phenyl-1-propene, followed by a subsequent insertion reaction between the methyl ethyl group on 2-phenyl-1-propene and the nitrogen atom on TTC/ZTC. This process produces a stable cationic polymer that can be used in clinical pathology and carcinogenesis studies.</p>Formula:C9H10Purity:Min. 95%Molecular weight:118.18 g/mol
