1191-39-5

Basic information

• Product Name: N-DODECYLMETHACRYLAMIDE
• Synonyms: N-DODECYLMETHACRYLAMIDE;N-Dodecyl-2-methyl-2-propenamide;N-Laurylmethacrylamide;N-dodecyl-2-methyl-prop-2-enamide;N-dodecyl-2-methylprop-2-enamide;N-lauryl-2-methyl-acrylamide
• CAS NO: 1191-39-5
• Molecular Formula: C₁₆H₃₁NO
• Molecular Weight: 253.42
• EINECS: 214-733-0
• Product Categories: monomer
• Mol File: 1191-39-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 145°C 0,8mm
• Flash Point: 239.5°C
• Appearance: /
• Density: 0.863g/cm³
• Vapor Pressure: 3.05E-06mmHg at 25°C
• Refractive Index: 1.453
• CAS DataBase Reference: N-DODECYLMETHACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-DODECYLMETHACRYLAMIDE(1191-39-5)
• EPA Substance Registry System: N-DODECYLMETHACRYLAMIDE(1191-39-5)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 1191-39-5(Hazardous Substances Data)

Usage

General Description

N-Dodecylmethacrylamide is a chemical compound that belongs to the class of methacrylamide monomers. It is a long-chain alkyl acrylamide with a dodecyl group attached to the nitrogen atom. This chemical is commonly used in the production of polymeric materials such as hydrogels, adhesives, and coatings. It is also used in the synthesis of polymers for various applications including drug delivery systems, tissue engineering, and controlled release formulations. N-Dodecylmethacrylamide is known for its high stability and compatibility with other monomers, making it a valuable component in the formulation of advanced polymeric materials. Additionally, it is used as a surfactant in various industrial and household products.

InChI:InChI=1/C16H31NO/c1-4-5-6-7-8-9-10-11-12-13-14-17-16(18)15(2)3/h2,4-14H2,1,3H3,(H,17,18)

Upstream product

• 124-22-1 n-Dodecylamine 
• 920-46-7 Methacryloyl chloride 

Relevant articles and documents

METHOD OF PRODUCING N-SUBSTITUTED (METH)ACRYLAMIDE

PROBLEM TO BE SOLVED: To provide a method of producing N-substituted (meth)acrylamide of high purity under mild conditions. SOLUTION: This invention relates to a method of obtaining N-substituted (meth)acrylamide [3] by the detachment of an amine compound through the liquid-phase thermal decomposition of an aminopropionic acid amide derivative [1] in the presence of a catalyst mainly composed of silica, wherein R1-R5 are represented by H, a C1-32 alkyl group, and a hydroxyalkyl group. COPYRIGHT: (C)2016,JPOandINPIT

Tuning linear copolymers into protein-specific hosts

Being picky: A new concept for selective protein recognition by artificial receptor molecules involves statistical copolymerization of simple binding monomers in defined stoichiometric ratios. As an example of its efficiency, an arginine-rich lysozyme is recognized by a bisphosphonate-rich copolymer with a remarkable Kd value of 25 nM, 100-times superior to that of cytochrome c, which is comparable in size and isoelectric point. (Chemical Equation Presented).