What is the n-Butyl acrylate?

n-Butyl acrylate is clear colorless Liquid, while it's Molecular Formula is C7H12O2. clear colorless Liquid Used in Adhesives and Sealants Industry: n-Butyl acrylate is used as a key component in the formulation of adhesives and sealants for various applications, such as bonding and sealing materials in construction, automotive, and packaging industries. Its high reactivity and ability to form strong bonds contribute to the performance and durability of these products. Used in Coatings and Paints Industry: n-Butyl acrylate is used as a co-monomer in the production of coatings and paints, including varnishes and inks. It enhances the properties of the final material, such as adhesion, flexibility, and durability, making it suitable for a wide range of applications, from architectural coatings to industrial finishes. Used in Textile, Paper, and Leather Industry: n-Butyl acrylate is utilized in the manufacture of textiles, paper, and leather products to improve their properties, such as water resistance, durability, and flexibility. Its incorporation into these materials enhances their performance and extends their lifespan. Used in Synthesis of Copolymers: n-Butyl acrylate is used as a co-monomer in the synthesis of copolymers to modify and enhance the properties of the final material. Its reactivity allows for the creation of copolymers with improved characteristics, such as increased strength, flexibility, and resistance to environmental factors. However, it is important to note that exposure to n-Butyl acrylate can cause irritations to the skin, eyes, and respiratory system, and long-term exposure may have harmful effects on human health. Therefore, appropriate safety measures should be in place when working with this chemical to ensure the well-being of individuals and the environment.

What is the CAS number for n-Butyl acrylate?

The CAS number of n-Butyl acrylate is 141-32-2.

What is n-Butyl acrylate (141-32-2) used for?

n-Butyl acrylate is a chemical compound that belongs to the acrylate monomer family, characterized by its clear, flammable liquid form with a fruity odor. It is highly reactive and prone to polymerization if not stored and handled properly, making it a versatile component in the production of polymers and coatings.InChI:InChI=1/C7H12O2/c1-3-4-5-6(2)7(8)9/h2-5H2,1H3,(H,8,9)/p-1

What is the n-Butyl acrylate?

n-Butyl acrylate is clear colorless Liquid, while it's Molecular Formula is C7H12O2. clear colorless Liquid Used in Adhesives and Sealants Industry: n-Butyl acrylate is used as a key component in the formulation of adhesives and sealants for various applications, such as bonding and sealing materials in construction, automotive, and packaging industries. Its high reactivity and ability to form strong bonds contribute to the performance and durability of these products. Used in Coatings and Paints Industry: n-Butyl acrylate is used as a co-monomer in the production of coatings and paints, including varnishes and inks. It enhances the properties of the final material, such as adhesion, flexibility, and durability, making it suitable for a wide range of applications, from architectural coatings to industrial finishes. Used in Textile, Paper, and Leather Industry: n-Butyl acrylate is utilized in the manufacture of textiles, paper, and leather products to improve their properties, such as water resistance, durability, and flexibility. Its incorporation into these materials enhances their performance and extends their lifespan. Used in Synthesis of Copolymers: n-Butyl acrylate is used as a co-monomer in the synthesis of copolymers to modify and enhance the properties of the final material. Its reactivity allows for the creation of copolymers with improved characteristics, such as increased strength, flexibility, and resistance to environmental factors. However, it is important to note that exposure to n-Butyl acrylate can cause irritations to the skin, eyes, and respiratory system, and long-term exposure may have harmful effects on human health. Therefore, appropriate safety measures should be in place when working with this chemical to ensure the well-being of individuals and the environment.

What is the CAS number for n-Butyl acrylate?

The CAS number of n-Butyl acrylate is 141-32-2.

What is n-Butyl acrylate (141-32-2) used for?

n-Butyl acrylate is a chemical compound that belongs to the acrylate monomer family, characterized by its clear, flammable liquid form with a fruity odor. It is highly reactive and prone to polymerization if not stored and handled properly, making it a versatile component in the production of polymers and coatings.InChI:InChI=1/C7H12O2/c1-3-4-5-6(2)7(8)9/h2-5H2,1H3,(H,8,9)/p-1

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141-32-2

Product Name：Butyl Acrylate
Molecular Formula：C₇H₁₂O₂
Purity：99%
Molecular Weight：128.171

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Product Details

Bulk supply high purity Butyl Acrylate 141-32-2, Paid sample available

Molecular Formula:C7H12O2
Molecular Weight:128.171
Appearance/Colour:clear colorless Liquid
Vapor Pressure:0.039mmHg at 25°C
Melting Point:-69 °C
Refractive Index:n20/D 1.410(lit.)
Boiling Point:145.9 °C at 760 mmHg
Flash Point:39.4 °C
PSA：26.30000
Density:0.898 g/cm³
LogP:1.51570

n-Butyl acrylate(Cas 141-32-2) Usage

General Description

n-Butyl acrylate is a chemical compound belonging to the family of acrylate monomers, commonly used in the production of polymers and coatings. It is a clear, flammable liquid with a fruity odor and is highly reactive with a potential for polymerization if not properly stored and handled. n-Butyl acrylate is primarily used in the production of adhesives, sealants, and coatings for various applications such as paints, varnishes, and inks. It is also utilized in the manufacture of textiles, paper, and leather products and as a co-monomer in the synthesis of copolymers to enhance the properties of the final material. However, exposure to n-Butyl acrylate can cause irritations to the skin, eyes, and respiratory system, and long-term exposure may have harmful effects on human health. Therefore, it should be handled with care and appropriate safety measures should be in place when working with this chemical.

InChI:InChI=1/C7H12O2/c1-3-4-5-6(2)7(8)9/h2-5H2,1H3,(H,8,9)/p-1

141-32-2 Relevant articles

Kinetics of the synthesis of propyl and butyl acrylates in the presence of some heteropolyacids as catalysts

Skrzypek, Ierzy,Witczak, Teresa,Grzesik, MirosLaw,Witczak, Mariusz

, p. 12 - 17 (2009)

Esterification reactions of acrylic acid...

Electrocatalytic Oxidation of Allylic Ethers, Dihydropyran and Phenol Using a Polypyridyl Complex of Ruthenium(IV)

Campos, Jose Luiz,Giovani, Wagner F. De,Romero, Jose Ricardo

, p. 597 - 599 (1990)

An electrocatalytic procedure is describ...

Silica-Supported zirconium complexes and their polyoligosilsesquioxane analogues in the transesterification of acrylates: Part 2. activity, recycling and regeneration

Salinier, Valerie,Niccolai, Geraldp,Dufaud, Veronique,Basset, Jean-Marie

, p. 2168 - 2177 (2009)

The catalytic activity of both supported...

Acrylate Esters by Ethenolysis of Maleate Esters with Ru Metathesis Catalysts: an HTE and a Technoeconomic Study

Copéret, Christophe,De Jesus Silva, Jordan,Engl, Pascal S.,Fedorov, Alexey,Lange, Jean-Paul,Togni, Antonio,Tsygankov, Alexey

, (2020)

A high throughput experimentation (HTE) ...

SYNTHESIS OF ACRYLIC ESTERS BY LIPASE

Ikeda, Isao,Tanaka, Jun,Suzuki, Kimihiro

, p. 6865 - 6866 (1991)

Various acrylic esters were synthesized ...

Acid- And base-switched palladium-catalyzed γ-C(sp3)-H alkylation and alkenylation of neopentylamine

Zhang, Jinquan,Zhang, Shuaizhong,Zou, Hongbin

supporting information, p. 3466 - 3471 (2021/05/31)

The functionalization of remote unactiva...

Palladium-catalyzed remote C-H functionalization of 2-aminopyrimidines

Das, Animesh,Jana, Akash,Maji, Biplab

supporting information, p. 4284 - 4287 (2020/04/27)

A straightforward strategy was developed...

Synthesis of Some Aromatic and Aliphatic Esters Using WO3/ZrO2 Solid Acid Catalyst under Solvent Free Conditions

Guguloth, Vijaya Charan,Battu, Satyanarayana

, p. 2153 - 2157 (2020/09/16)

A simple method is delineated for the sy...

Second-Generation meta-Phenolsulfonic Acid-Formaldehyde Resin as a Catalyst for Continuous-Flow Esterification

Hu, Hao,Ota, Hajime,Baek, Heeyoel,Shinohara, Kenta,Mase, Toshiaki,Uozumi, Yasuhiro,Yamada, Yoichi M. A.

supporting information, p. 160 - 163 (2020/01/02)

A second-generation m-phenolsulfonic aci...

141-32-2 Process route

: 74-85-1
ethene

: 52392-64-0,52392-65-1,538-65-8
n-butyl cinnamate

: 141-32-2,9003-49-0
acrylic acid n-butyl ester

: 588-59-0
stilbene

Conditions

Conditions	Yield
With Hoveyda-Grubbs catalyst second generation; In dichloromethane; at 40 ℃; for 24h; under 750.075 Torr; Pressure; Concentration; Inert atmosphere; Green chemistry;