522864
Methylstyrene
60% meta, 40% para and 1% ortho, 99%, contains ~50 ppm 4-tert-butylcatechol as inhibitor
Synonym(s):
Vinyltoluene
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
CH3C6H4CH=CH2
CAS Number:
Molecular Weight:
118.18
Beilstein:
1209317
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
Quality Level
Assay
99%
contains
~50 ppm 4-tert-butylcatechol as inhibitor
refractive index
n20/D 1.5425 (lit.)
bp
168 °C (lit.)
density
0.893 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
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
InChI key
VAPKHDZBJXRVNG-UHFFFAOYSA-N
Related Categories
General description
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).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
125.6 °F - closed cup
Flash Point(C)
52 °C - closed cup
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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.
Rainer M Vallant et al.
Journal of proteome research, 6(1), 44-53 (2007-01-06)
60]fullerene derivatives (dioctadecyl methano[60]fullerene, [60]fullerenoacetic acid, and IDA-[60]fullerene) were prepared and subjected to a comprehensive characterization study including protein binding properties and capacity. These fullerene derivatives were successfully applied as material-enhanced laser desorption/ionization (MELDI) carrier materials. It is shown that
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
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
Sandra C Greer
Annual review of physical chemistry, 53, 173-200 (2002-04-25)
The aggregation of monomers into polymers, whether by covalent or noncovalent interactions, is often reversible and frequently occurs with the entropy and enthalpy of the aggregation sharing the same sign. In such a case, the aggregation goes forward or reverses
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service