ChemicalBook > CAS DataBase List > 4-Acetoxystyrene

4-Acetoxystyrene

Product Name
4-Acetoxystyrene
CAS No.
2628-16-2
Chemical Name
4-Acetoxystyrene
Synonyms
4-VINYLPHENYL ACETATE;4-ETHENYLPHENOL ACETATE;P-ACETOXYSTYRENE;(4-Ethenylphenyl) acetate;Phenol, 4-ethenyl-, acetate;Phenol, 4-ethenyl-,1-acetate;VPAC;c-908;ACS/ASM;ACETOXYSTYRENE
CBNumber
CB9777268
Molecular Formula
C10H10O2
Formula Weight
162.19
MOL File
2628-16-2.mol
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4-Acetoxystyrene Property

Melting point:
7-8 °C (lit.)
Boiling point:
260 °C (lit.)
Density 
1.06 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.538(lit.)
Flash point:
190 °F
storage temp. 
2-8°C
form 
Liquid
color 
Clear colorless
BRN 
1862793
InChI
InChI=1S/C10H10O2/c1-3-9-4-6-10(7-5-9)12-8(2)11/h3-7H,1H2,2H3
InChIKey
JAMNSIXSLVPNLC-UHFFFAOYSA-N
SMILES
C1(OC(=O)C)=CC=C(C=C)C=C1
CAS DataBase Reference
2628-16-2(CAS DataBase Reference)
NIST Chemistry Reference
Phenol, 4-ethenyl-, acetate(2628-16-2)
EPA Substance Registry System
Phenol, 4-ethenyl-, acetate (2628-16-2)
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Safety

Hazard Codes 
Xn
Risk Statements 
22-38-43-36/38
Safety Statements 
36/37-26
RIDADR 
2810
WGK Germany 
3
RTECS 
SL3784000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29153900
Toxicity
LD50 orl-rat: 1503 mg/kg EPASR* 8EHQ-1190-1082
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
380547
Product name
4-Acetoxystyrene
Purity
96%, contains 200-300 ppm monomethyl ether hydroquinone as inhibitor
Packaging
25ml
Price
$142
Updated
2024/03/01
Sigma-Aldrich
Product number
380547
Product name
4-Acetoxystyrene
Purity
96%, contains 200-300 ppm monomethyl ether hydroquinone as inhibitor
Packaging
5ml
Price
$48.7
Updated
2023/06/20
TCI Chemical
Product number
A1551
Product name
4-Vinylphenyl Acetate (stabilized with TBC)
Purity
>98.0%(GC)
Packaging
5g
Price
$30
Updated
2024/03/01
TCI Chemical
Product number
A1551
Product name
4-Vinylphenyl Acetate (stabilized with TBC)
Purity
>98.0%(GC)
Packaging
25g
Price
$112
Updated
2024/03/01
Alfa Aesar
Product number
L11601
Product name
4-Acetoxystyrene, 95%, stab.
Packaging
2g
Price
$20.65
Updated
2024/03/01
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4-Acetoxystyrene Chemical Properties,Usage,Production

Description

4-Acetoxystyrene can be used to synthesize Poly(p-hydroxystyrene) as the main component of photoresist. The chemically amplified photoresist of the poly(p-hydroxystyrene) series is currently the mainstream photoresist product in the world, and it is one of the key technologies for processing photo-etched integrated circuits and manufacturing chips.

Chemical Properties

4-Acetoxystyrene is a clear and colorless liquid that is essentially the acetic acid ester of p-vinylphenol. It will homopolymerize readily in the same manner that styrene homopolymerizes and can also be copolymerized with styrene and with monomers which are copolymerizable with styrene. 4-Acetoxystyrene is homopolymerized and copolymerized in aqueous emulsion and, without isolation, the polymer is hydrolyzed to homopolymers and copolymers of p-vinylphenol with a base. Homopolymers and copolymers of p-vinylphenol are used as epoxy resin curing agents and in the preparation of epoxy resins by reaction with epichlorohydrin.

Uses

4-Acetoxystyrene is a stable Styrene monomer which can be readily polymerized and copolymerized to low, medium and high molecular weight polymers. Undergoes free radical polymerization, similar to styrene.

Preparation

The preparation of 4-Acetoxystyrene is as follows:Add p-hydroxystyrene (120g) to a 2L four-neck bottle. triethylamine(106g), phenothiazine (1.2g), Methyl tert-butyl ether (480 g), Dry ice-ethanol bath to -5 to 0 °C, acetyl chloride (86g) was added dropwise with stirring. The internal temperature is controlled at -5 to 0 °C. After the completion of the dropwise addition, the temperature was raised at 10 to 20 °C to continue the reaction for 1 hour. Sampling analysis (central control 1, raw material After completion of the reaction, the mixture was filtered, and the cake was washed with methyl t-butyl ether (50 g × 3). The filtrate was quenched by the addition of 4 g of methanol, and the reaction was stirred for 10 minutes. After completion, phenothiazine (1.2 g) was added and the reaction mixture was concentrated.Methyl tert-butyl ether (580 g) was recovered to give a crude product (160 g).The crude product was distilled under reduced pressure to give the product, p-acetoxy styrene (142 g), yield 87.7%, and sampled for analysis (main content >99%).

Application

4-Acetoxystyrene is a polymer that can be used in microlithography and is the precursor of easily derivatized p-hydroxystyrene.

Hazard

4-Acetoxystyrene is a flammable liquid and can cause skin and eye irritation upon contact.

Flammability and Explosibility

Not classified

Safety Profile

Moderately toxic by ingestion.Slightly toxic by skin contact. An eye irritant. A combustibleliquid. When heated to decomposition it emits acrid smokeand irritating vapors.

storage

4-Acetoxystyrene should be handled with proper safety precautions and stored in a cool, dry place away from sources of ignition.

Advantages

Grafting 4-Acetoxystyrene (AOS) onto Polypropylene (PP) could significantly improved PP's space charge distribution, DC resistivity, and DC breakdown strength. These improvements were related to carbonyl (polar group) and benzene ring derived from AOS. As the carbonyl in AOS is introduced onto the PP chains by the grafting reaction, the homo-charge injected from the electrodes during the voltage application is trapped by the carbonyl and neutralizes the hetero-charge, decreasing hetero-charge. With the increase of grafting degree, the concentration of carbonyl increases, the corresponding charge trapping ability rises, and thus the extent of neutralizing the hetero-charge increases. The space charge is effectively suppressed. Grafting AOS onto PP significantly increases breakdown performance since AOS possesses chemical construction similar to the benzil-type voltage stabilizer. Because of delocalized π-electrons, AOS possesses a low ionizing potential and high electron affinity, making it capable of capturing the energetic electrons by collision and dissipating the energy, and the breakdown strength is improved. On the other hand, the energy of hot electrons is consumed through Fries rearrangement of AOS, weakening the attack of hot electrons on molecular chains and resulting in enhanced breakdown strength[1].

References

[1] Yue Liang. “Preparation and electrical properties of 4-acetoxystyrene grafted polypropylene for HVDC cable insulation.” Journal of Materials Science: Materials in Electronics 31 5 (2020): 3890–3898.

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View Lastest Price from 4-Acetoxystyrene manufacturers

HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
4-Acetoxystyrene 2628-16-2
Price
US $999.00-800.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000
Release date
2024-08-21
Hebei Zhuanglai Chemical Trading Co Ltd
Product
4-Ethenylphenol acetate 2628-16-2
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 ton
Release date
2024-12-19
Shanghai Qyubiotech Co., Ltd.
Product
4-Ethenylphenol acetate 2628-16-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%+
Supply Ability
1000000kg per Month
Release date
2023-04-10

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