Skip to Content
Merck
All Photos(2)

Key Documents

522864

Sigma-Aldrich

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


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

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

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 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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Sequence-Controlled alpha-Methylstyrene/Styrene Copolymers: Syntheses and Sequence Distribution Resolution
Arnaud Wolf, et al.
Macromolecules, 53, 8032-8040 (2020)
Xiang Zhang et al.
Rapid communications in mass spectrometry : RCM, 20(12), 1877-1882 (2006-05-24)
The interaction of the nitroxide radical traps (Tempo and Dmpo) and radicals produced in the electrophilic fluorination of olefins (styrene and alpha-methylstyrene) and Selectfluor (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octanebis(tetrafluoroborate) (F-TEDA-BF(4)) (1)) was investigated by electrospray ionization mass spectrometry (ESI-MS). Tempo succeeded in intercepting the
Christine H Petter et al.
Journal of separation science, 31(14), 2541-2550 (2008-08-12)
The design of novel stationary phases is a permanent demanding challenge in chromatographic separation science to enable analysis with enhanced selectivity, specificity and speed. Therefore, the characterisation of chemical and physical properties is next to calculation of chromatographic parameters essential.
Jordi Benet-Buchholz et al.
Dalton transactions (Cambridge, England : 2003), (30)(30), 5910-5923 (2009-07-23)
The synthesis and the full characterization of a new ruthenium(II) complex with the pentadentate bispidine ligand L(1) is reported and shown to be a very active catalyst for olefin epoxidation. The selectivity in the epoxidation of cis- and trans-beta-methylstyrene with
Jing Huang et al.
Dalton transactions (Cambridge, England : 2003), 41(35), 10661-10669 (2012-07-31)
A series of chiral salen Mn(III) immobilized onto azole onium modified zinc poly(styrene-phenylvinyl phosphonate)-phosphate (ZnPS-PVPA) were prepared. The catalysts were characterized by FT-IR, diffusion reflection UV-vis, AAS, N(2) volumetric adsorption, SEM, TEM, XPS, XRD, TG and elemental analysis. The results

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