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Sigma-Aldrich

Methylstyrene

60% meta, 40% para and 1% ortho, 99%, contains ~50 ppm 4-tert-butylcatechol as inhibitor

Synonyme(s) :

Vinyltoluene

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About This Item

Formule linéaire :
CH3C6H4CH=CH2
Numéro CAS:
25013-15-4
Poids moléculaire :
118.18
Numéro Beilstein :
1209317
Numéro CE :
246-562-2
Numéro MDL:
MFCD00168066
Code UNSPSC :
12162002
ID de substance PubChem :
24874126
Nomenclature NACRES :
NA.23

Pureté

99%

Contient

~50 ppm 4-tert-butylcatechol as inhibitor

Indice de réfraction

n20/D 1.5425 (lit.)

Point d'ébullition

168 °C (lit.)

Densité

0.893 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

Cc1ccc(C=C)cc1.Cc2cccc(C=C)c2

InChI

1S/2C9H10/c1-3-9-6-4-8(2)5-7-9;1-3-9-6-4-5-8(2)7-9/h2*3-7H,1H2,2H3

Clé InChI

VAPKHDZBJXRVNG-UHFFFAOYSA-N

Catégories apparentées

Description générale

Methylstyrene can be used as a monomer in the synthesis of block copolymers for resins and adhesives. It is widely used as a starting material to prepare latexes for paper coating applications.

Application



  • Applications in cancer therapy: Investigation into (−)-Epicatechin incorporated in phytopharmaceuticals for cancer treatment discusses its bioactive properties and synergistic effects when combined with other therapeutic agents, providing new avenues for integrative cancer therapies (Idoudi et al., 2024).



Pictogrammes

FlameHealth hazardExclamation mark
GHS02,GHS08,GHS07

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Inhalation - 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 3

Point d'éclair (°F)

125.6 °F - closed cup

Point d'éclair (°C)

52 °C - closed cup

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Jay A Grobler et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(10), 6661-6666 (2002-05-09)
The process of integrating the reverse-transcribed HIV-1 DNA into the host chromosomal DNA is catalyzed by the virally encoded enzyme integrase (IN). Integration requires two metal-dependent reactions, 3' end processing and strand transfer. Compounds that contain a diketo acid moiety
M Groner et al.
Marine pollution bulletin, 42(10), 935-941 (2001-11-06)
The chemical identities of several organic compounds that dominate the ultraviolet (UV) fluorescence of water after exposure to gasoline, diesel fuel and crude oil are presented. A combination of high-performance liquid chromatography with UV-fluorescence detection, fluorescence spectroscopy and gas chromatography-mass
J A Cohen et al.
The journal of physical chemistry. B, 113(12), 3709-3714 (2009-03-07)
We present a phenomenological one-parameter scaling equation of state that accurately represents osmotic pressures of neutral flexible polymers in good solvents from the dilute through the semidilute regime. The equation comprises a sum of scaled van't Hoff and des Cloizeaux
Christopher P Burke et al.
The Journal of organic chemistry, 72(16), 6320-6323 (2007-07-12)
Asymmetric epoxidation of various olefins with an N-aryl-substituted oxazolidinone-containing ketone as catalyst and hydrogen peroxide as the primary oxidant has been investigated, and up to 96% ee was obtained.
Henry Dube et al.
Journal of the American Chemical Society, 132(29), 9984-9985 (2010-07-09)
The trans to cis isomerization of 4,4'-dimethylazobenzene by the nonchemical stimuli light and heat alters its guest binding properties, allowing control over encapsulation of a second guest. We show here how this remote control for reversible encapsulation can be used
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