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522864

Sigma-Aldrich

Methylstyrene

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

Sinonimo/i:

Vinyltoluene

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250 ML
41,10 €
1 L
123,00 €

41,10 €

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250 ML
41,10 €
1 L
123,00 €

About This Item

Formula condensata:
CH3C6H4CH=CH2
Numero CAS:
25013-15-4
Peso molecolare:
118.18
Beilstein:
1209317
Numero CE:
246-562-2
Numero MDL:
MFCD00168066
Codice UNSPSC:
12162002
ID PubChem:
24874126
NACRES:
NA.23

41,10 €

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Livello qualitativo

200

Saggio

99%

contiene

~50 ppm 4-tert-butylcatechol as inhibitor

Indice di rifrazione

n20/D 1.5425 (lit.)

P. ebollizione

168 °C (lit.)

Densità

0.893 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

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
VAPKHDZBJXRVNG-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

Methylstyrene can be used as a monomer in the synthesis of block copolymers for resins and adhesives.[1] [2] It is widely used as a starting material to prepare latexes for paper coating applications.[3]

Applicazioni



  • 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).



Avvertenze

Danger

Indicazioni di pericolo

H226,H304,H315,H319,H332,H335

Classi di pericolo

Acute Tox. 4 Inhalation - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

125.6 °F - closed cup

Punto d’infiammabilità (°C)

52 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
MKCX5234
MKCW6857
MKCV0446
MKCP1055
MKCR5794

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Sigma-Aldrich

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Sigma-Aldrich

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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
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
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
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
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