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N,N-DI-N-BUTYLACRYLAMIDE, a member of the acrylamide derivatives family, is a chemical compound widely recognized for its high stability and resistance to adverse environmental conditions. Its robust properties make it a valuable component in the creation of polymers and copolymers, which are integral to numerous industrial applications.

2274-13-7

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2274-13-7 Usage

Uses

Used in Polymer and Copolymer Production:
N,N-DI-N-BUTYLACRYLAMIDE is utilized as a key component in the synthesis of polymers and copolymers, contributing to their enhanced stability and performance. Its presence in these materials is crucial for achieving desired properties such as strength, flexibility, and durability.
Used in Adhesives Industry:
In the adhesives industry, N,N-DI-N-BUTYLACRYLAMIDE is employed as a critical ingredient for formulating high-performance adhesives. Its inclusion improves the adhesive's bonding strength, resistance to environmental factors, and overall durability, making it suitable for various applications, including construction, automotive, and packaging.
Used in Coatings Industry:
N,N-DI-N-BUTYLACRYLAMIDE is used as a vital additive in the coatings industry to enhance the protective and decorative qualities of coatings. Its integration into coating formulations results in improved resistance to wear, chemicals, and UV radiation, ensuring the longevity and appearance of coated surfaces.
Used in Textile Industry:
Within the textile industry, N,N-DI-N-BUTYLACRYLAMIDE serves as an essential component in the development of advanced textile materials. Its contribution to the fabric's composition endows textiles with increased resistance to abrasion, stains, and environmental stress, catering to the needs of various end-use applications, such as outdoor apparel and industrial fabrics.
It is imperative to handle N,N-DI-N-BUTYLACRYLAMIDE with caution due to its potential health and environmental risks. Proper management and disposal practices are essential to mitigate any adverse effects associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 2274-13-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2274-13:
(6*2)+(5*2)+(4*7)+(3*4)+(2*1)+(1*3)=67
67 % 10 = 7
So 2274-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO/c1-4-7-9-12(10-8-5-2)11(13)6-3/h6H,3-5,7-10H2,1-2H3

2274-13-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dibutylprop-2-enamide

1.2 Other means of identification

Product number -
Other names N,N-Dibutyl-acrylamid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2274-13-7 SDS

2274-13-7Relevant academic research and scientific papers

Translating Thermal Response of Triblock Copolymer Assemblies in Dilute Solution to Macroscopic Gelation and Phase Separation

Sun, Zhe,Tian, Ye,Hom, Wendy L.,Gang, Oleg,Bhatia, Surita R.,Grubbs, Robert B.

, p. 1491 - 1494 (2017)

The thermal response of semi-dilute solutions (5 w/w%) of two amphiphilic thermoresponsive poly(ethylene oxide)-b-poly(N,N-diethylacrylamide)-b-poly(N,N-dibutylacrylamide) (PEO45-PDEAmx-PDBAm12) triblock copolymers, which

Some unusual reactivities in the SmI2-mediated reductive coupling of acrylamides and acrylates with imides

Taaning, Rolf H.,Lindsay, Karl B.,Skrydstrup, Troels

experimental part, p. 10908 - 10916 (2010/02/27)

A serendipitous discovery of some intra-molecular enolate addition reactions following a SmI2-mediated reductive cross-coupling between imides and electron-deficient olefins leading to some novel compounds was investigated to determine the generality of the protocol and the possible mechanistic pathways involved. This provided a Z-selective synthesis of γ-ketoenediamides in good yields, albeit as of now the substrate scope remains limited. It was also shown that the seemingly similar acrylate substrates can behave differently compared to the corresponding acrylamides in their SmI2-mediated reductive cross-coupling reaction with imides, and it was argued that these diverging reactivities are dominated by the ability of the acrylates to coordinate the samarium metal centre.

Synthesis of N,N-disubstituted (meth)acrylamides

Kazakov,Kazantsev,Shirshin,Danov,Igolkin,Afon'shin

, p. 912 - 913 (2007/10/03)

N,N-Dialkyl(meth)acrylamides were prepared in 79-96% yields by reaction of N,N,N',N'-tetraalkylmethylenediamines with (meth)acryloyl chloride.

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