1506-53-2

Basic information

• Product Name: N-DODECYLACRYLAMIDE
• Synonyms: N-DODECYLACRYLAMIDE;N-Laurylacrylamide;N-dodecylprop-2-enamide;2-Propenamide,N-dodecyl-;N-Dodecylacrylamide
• CAS NO: 1506-53-2
• Molecular Formula: C₁₅H₂₉NO
• Molecular Weight: 239.4
• EINECS: 216-136-0
• Mol File: 1506-53-2.mol
• Article Data: 9

Chemical Properties

• Melting Point: 58 °C
• Boiling Point: 155 °C / 1mmHg
• Flash Point: 229.74 °C
• Appearance: /
• Density: 0.864 g/cm³
• Vapor Pressure: 8.41E-06mmHg at 25°C
• Refractive Index: 1.452
• PKA: 15.03±0.46(Predicted)
• CAS DataBase Reference: N-DODECYLACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-DODECYLACRYLAMIDE(1506-53-2)
• EPA Substance Registry System: N-DODECYLACRYLAMIDE(1506-53-2)

Safety Data

• Hazardous Substances Data: 1506-53-2(Hazardous Substances Data)

Usage

General Description

N-dodecylacrylamide is a chemical compound with the molecular formula C16H31NO and a molecular weight of 257.43 g/mol. It is an acrylamide derivative and is classified as a nonionic surfactant. N-dodecylacrylamide is commonly used in the production of polymers and as a building block for the synthesis of various polymeric materials. It is also employed in the formulation of personal care products, such as shampoos and conditioners, as well as in the manufacturing of adhesives, coatings, and lubricants. N-dodecylacrylamide is known for its ability to reduce surface tension and enhance wetting and spreading properties in various industrial and consumer applications. Additionally, it is considered to be relatively safe for use in these products, with low toxicity and minimal potential for skin irritation.

InChI:InChI=1/C15H29NO/c1-3-5-6-7-8-9-10-11-12-13-14-16-15(17)4-2/h4H,2-3,5-14H2,1H3,(H,16,17)

Upstream product

• 124-22-1 n-Dodecylamine 
• 814-68-6 acryloyl chloride 
• 112-16-3 n-dodecanoyl chloride 
• 79-06-1 2-propenamide 
• 143-15-7 1-dodecylbromide 
• 15438-67-2 (3-methoxypropyl)amide 
• 2651-43-6 3-hydroxypropionamide 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 79-10-7 acrylic acid 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 619-73-8 4-nitrobenzyl chloride 
• 62-23-7 4-nitro-benzoic acid 
• 1093682-75-7 1-benzylaziridine-2-(N-n-dodecyl)carboxamide 
• 1093682-78-0 1-(p-methoxybenzyl)aziridine-2-(N-n-dodecyl)carboxamide 
• 1018998-95-2 C₈₈H₁₆₉N₉O₅ 
• 1018998-89-4 C₈₉H₁₆₉N₉O₇ 
• 1018998-83-8 C₈₉H₁₆₉N₉O₇ 
• 1018998-77-0 C₅₂H₈₈N₆O₆ 
• 1018998-79-2 C₆₇H₁₁₇N₇O₇ 
• 1018998-81-6 C₈₂H₁₄₆N₈O₈ 
• 274904-56-2 3-(4-{4-[4-((E)-2-tert-butyloxycarbonyl-vinyl)phenyl]-5-[4-(2-dodecylcarbamoyl-vinyl)phenyl]-1H-imidazol-2-yl}phenyl)-isoxazole-5-carboxylic acid ethyl ester 
• 274904-26-6 (E)-3-(4-{2-[4-((E)-2-Dodecylcarbamoyl-vinyl)-phenyl]-2-oxo-acetyl}-phenyl)-acrylic acid tert-butyl ester 

Relevant articles and documents

Reactivity of secondary N-alkyl acrylamides in Morita–Baylis–Hillman reactions

The Morita–Baylis–Hillman (MBH) reaction of secondary N-alkyl acrylamides, discarded up to now from investigations of the scope of activated alkenes, was studied. Optimization of the reaction conditions revealed that a balance must be found between activation of the MBH coupling reaction and that of the undesired competitive aldehyde Cannizzaro reaction. Using 3-Hydroxyquinuclidine (3-HQD) in a 1:1 water-2-MeTHF mixture provides the appropriate conditions that were applicable to a wide range of diversely substituted secondary N-alkyl acrylamides and aromatic aldehydes, giving rise to novel amide-containing MBH adducts under mild and clean conditions.

Direct Deuteration of Acrylic and Methacrylic Acid Derivatives Catalyzed by Platinum on Carbon in Deuterium Oxide

The platinum on carbon (Pt/C)-catalyzed deuteration of acrylic and methacrylic acid derivatives in deuterium oxide (D2O) efficiently proceeded to give the corresponding acrylic acid-d3 and methacrylic acid-d5 derivatives. The olefinic functionality, as well as the methyl group on the unsaturated functionality of the substrate, were satisfactorily deuterated via the hydrogen (H)-deuterium (D) exchange reaction. The obtained deuterated compounds are useful building blocks and efficiently converted to the corresponding desired products including a polymer without the degradation of the original deuterium contents. (Figure presented.).

N-alkyl acrylamide intermediate and preparation method thereof and preparation method of N-alkyl acrylamide

The invention belongs to the field of acrylamide, and particularly relates to an N-alkyl acrylamide intermediate and a preparation method thereof and a preparation method of N-alkyl acrylamide.The preparation method of N-alkyl acrylamide comprises the following steps that a cracking reaction is conducted on a compound with the structure of a formula (I) in the presence of a cracking catalyst, and N-alkyl acrylamide with the structure of a formula (VII) is obtained, wherein R1 and R2 are independently selected from alkyl, and n is larger than or equal to 0 and smaller than or equal to 30.The yield of N-alkyl acrylamide prepared through the method is high.It is indicated through experimental results that the total yield of N-alkyl acrylamide prepared through the method is larger than 85%.Please see the formulas in the description.