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Sigma-Aldrich

tert-Butyl acrylate

contains 10-20 ppm monomethyl ether hydroquinone as inhibitor, 98%

Synonyme(s) :

t-Butyl acrylate

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About This Item

Formule linéaire :
CH2=CHCOOC(CH3)3
Numéro CAS:
Poids moléculaire :
128.17
Numéro Beilstein :
1742329
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Pureté

98%

Forme

liquid

Contient

10-20 ppm monomethyl ether hydroquinone as inhibitor

Indice de réfraction

n20/D 1.410 (lit.)

Point d'ébullition

61-63 °C/60 mmHg (lit.)

Densité

0.875 g/mL at 25 °C (lit.)

Chaîne SMILES 

CC(C)(C)OC(=O)C=C

InChI

1S/C7H12O2/c1-5-6(8)9-7(2,3)4/h5H,1H2,2-4H3

Clé InChI

ISXSCDLOGDJUNJ-UHFFFAOYSA-N

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Catégories apparentées

Description générale

tert-Butyl acrylate is an organic chemical compound that can be used as a monomer for the preparation of various types of polymers with desirable characteristics. It can undergo free-radical polymerization, which is a common method used to produce polymeric materials. Additionally, tert-butyl acrylate polymers can be copolymerized with other monomers to modify their properties. The versatility of tert-butyl acrylate makes it suitable for a wide range of applications, including coatings, adhesives, sealants, elastomers, and specialty films.

Application

tert-Butyl acrylate is a monomer used to produce poly(tert-butyl acrylate) (PtBA) polymers and copolymers, and poly(acrylic acid) polyelectrolyte brushes. It undergoes radiation polymerization to form TBA-gels for radio-fluorogenic dose imaging applications. The monomer can be used to synthesize Poly(t-butyl acrylate). It may be used as a reactive diluent in a study.

tert-Butyl acrylate can also be used as:
  • A building block in the synthesis of asymmetric membranes, which are potentially useful in filtration, separation, or gas permeation processes.
  • A monomer in the preparation of a siloxane-incorporated copolymer binder for silicon anodes in lithium-ion batteries.
  • A monomer in the synthesis of poly(tert-butyl acrylate)/carbon nanofiber (CNF) materials through atom transfer radical polymerization (ATRP).

Pictogrammes

FlameSkull and crossbonesEnvironment

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

62.6 °F - closed cup

Point d'éclair (°C)

17 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Consulter la Bibliothèque de documents

Polymer-gel formation and reformation on irradiation of tertiary-butyl acrylate
Yao T, et al.
Radiation Physics and Chemistry, 97, 147-152 (2014)
Huanhuan Liu et al.
Polymers, 11(5) (2019-05-10)
Gambogenic acid (GNA) has been demonstrated with outstanding antitumor activity as a potential antitumor drug in recent years. However, the low solubility and deficient bioavailability of GNA seriously hinder its practical application in the clinic area. In this study, a
Study of the kinetics of step and flash imprint lithography photopolymerization.
Dickey MD, et al.
AIChE Journal, 51(9), 2547-2555 (2005)
Calvin A Omolo et al.
Journal of liposome research, 31(1), 45-63 (2019-10-31)
pH responsive drug delivery systems are one of the new strategies to address the spread of bacterial resistance to currently used antibiotics. The aim of this study was to formulate liposomes with 'On' and 'Off'' pH responsive switches for infection
Hongli Zhao et al.
Journal of nanoscience and nanotechnology, 18(12), 8070-8077 (2018-09-08)
In this work, a novel combination of drug therapy and cryotherapy for tumor treatment was developed. Pluronic F127 modified with poly(acrylic acid) at two terminals (denoted as PAA-PF127-PAA) was used as carriers for doxorubicin (DOX) delivery. Due to the pH-sensitive

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