S4972
Styrene
≥99%, liquid, ReagentPlus®, contains 4-tert-butylcatechol as stabilizer
동의어(들):
Phenylethylene, Vinylbenzene
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5CH=CH2
CAS 번호:
Molecular Weight:
104.15
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
202-851-5
MDL number:
Beilstein/REAXYS Number:
1071236
Assay:
≥99%
Form:
liquid
제품 이름
Styrene, ReagentPlus®, contains 4-tert-butylcatechol as stabilizer, ≥99%
InChI key
PPBRXRYQALVLMV-UHFFFAOYSA-N
InChI
1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2
SMILES string
C=Cc1ccccc1
vapor density
3.6 (vs air)
vapor pressure
12.4 mmHg ( 37.7 °C), 4.3 mmHg ( 15 °C)
product line
ReagentPlus®
assay
≥99%
form
liquid
autoignition temp.
914 °F
contains
4-tert-butylcatechol as stabilizer
expl. lim.
6.1 %
Quality Level
refractive index
n20/D 1.546 (lit.)
bp
145-146 °C (lit.)
mp
−31 °C (lit.)
density
0.906 g/mL at 25 °C
functional group
phenyl
storage temp.
2-8°C
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General description
Removal of styrene from textile dyeing wastewater treatment plants (TDWTPs) has been investigated. Catalytic potential of the Co-SBA-15 for the oxidation of styrene with hydrogen peroxide has been investigated. Screening of asymmetric epoxidation of styrene by gas chromatography-mass spectrometry (GC-MS) with selected ion monitoring (SIM) has been reported. The homogeneous atom transfer radical polymerization (ATRP) of styrene by employing solubilizing 4,4′-dialkyl substituted 2,2′-bipyridines affords well-defined polymers. The Heck reaction of chlorobenzene and substituted chlorobenzenes with styrene in water using catalytic palladium on carbon affords 1,2-diphenylethane.
Application
Styrene has been used as a test styrene sample in a study involving the effect of reversible addition-fragmentation chain transfer (RAFT) controllers on its RAFT polymerization in supercritical carbon dioxide in the presence of poly(styrene-block-dimethylsiloxane) (PSDMS) as a stabilizer.
Styrene was used in the preparation of well-defined homopolymers, diblock copolymers and triblock copolymers of tert-butyl acrylate, methyl acrylate and styrene.
Other Notes
Inhibitor depletes over time especially at higher temperatures
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Inhalation - STOT SE 3
target_organs
hearing organs, Respiratory system
저장 등급
3 - Flammable liquids
wgk
WGK 2
flash_point_f
89.6 °F - closed cup
flash_point_c
32.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Heterogeneous palladium-catalysed heck reaction of aryl chlorides and styrene in water under mild conditions.
Mukhopadhyay S, et al.
Advanced Synthesis & Catalysis, 344(3-4), 348-354 (2002)
Xun-An Ning et al.
Chemosphere, 136, 50-55 (2015-05-02)
The occurrence and removal of benzene, toluene, ethylbenzene, xylenes, styrene and isopropylbenzene (BTEXSI) from 6 textile dyeing wastewater treatment plants (TDWTPs) were investigated in this study. The practical capacities of the 6 representative plants, which used the activated sludge process
Yao Mu et al.
Se pu = Chinese journal of chromatography, 32(12), 1385-1389 (2015-04-24)
A screening method by gas chromatography-mass spectrometry (GC-MS) with selected ion monitoring (SIM) has been developed for asymmetric epoxidation of styrene. All samples were analyzed by GC-MS with the mode of SIM by using ethylbenzene as the internal standard, by
Xiaojing Jin et al.
Journal of nanoscience and nanotechnology, 14(9), 7234-7241 (2015-05-01)
The rapid preparation of SBA-15 with cobalt (Co) introduction was performed via the ultrasonic irradiation in combination with "pH-adjusting" method. The catalytic properties of the synthesized Co-SBA-15 were investigated by examining the oxidation of styrene with hydrogen peroxide. The effect
The preparation of t-butyl acrylate, methyl acrylate, and styrene block copolymers by atom transfer radical polymerization: Precursors to amphiphilic and hydrophilic block copolymers and conversion to complex nanostructured materials.
Ma Q and Wooley KL.
Journal of Polymer Science Part A: Polymer Chemistry, 38(S1), 4805-4820 (2000)
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