2565-18-6

Basic information

• Product Name: N-N-BUTYLACRYLAMIDE
• Synonyms: N-N-BUTYLACRYLAMIDE;N-Butylacrylamide
• CAS NO: 2565-18-6
• Molecular Formula: C₇H₁₃NO
• Molecular Weight: 127.18
• Product Categories: monomer
• Mol File: 2565-18-6.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 83-85 °C(Press: 1 Torr)
• Appearance: /
• Density: 0.876±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 15.13±0.46(Predicted)
• CAS DataBase Reference: N-N-BUTYLACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-N-BUTYLACRYLAMIDE(2565-18-6)
• EPA Substance Registry System: N-N-BUTYLACRYLAMIDE(2565-18-6)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 2565-18-6(Hazardous Substances Data)

Usage

General Description

N-N-Butylacrylamide is an organic compound with the chemical formula C7H13NO. It is a colorless liquid that is used in the manufacturing of polymers and adhesives. N-N-BUTYLACRYLAMIDE is a type of acrylamide, which is known for its use in industrial and commercial applications. N-N-Butylacrylamide is used as a building block in the production of various polymers, including those used in water treatment, papermaking, and textiles. It is also used as a crosslinking agent in adhesives, providing increased strength and durability. Additionally, it can be used in the synthesis of pharmaceuticals and other specialty chemicals. However, it is important to handle N-N-Butylacrylamide with caution, as it is a known skin and eye irritant and can be harmful if ingested or inhaled.

Upstream product

• 105974-96-7 N,N'-dibutyl-3-aminopropanamide 
• 13108-03-7 3-chloro-propionic acid butylamide 
• 79-10-7 acrylic acid 
• 74-86-2 acetylene 
• 109-73-9 N-butylamine 
• 598-72-1 2-Bromopropionic acid 
• 590-92-1 3-Bromopropionic acid 
• 814-68-6 acryloyl chloride 
• 292638-85-8 acrylic acid methyl ester 
• 55711-80-3 N,N-Dibutyl-cis-β-jodacrylamid 
• 110-86-1 pyridine 

Downstream Products

• 101171-78-2 3,4-dimethyl-cyclohex-3-enecarboxylic acid butylamide 
• 86774-83-6 (E)-N-butyl-3-(2-hydroxyphenyl)acrylamide 
• 586-98-1 2-Hydroxymethylpyridine 
• 98-98-6 2-Picolinic acid 
• 619-25-0 3-Nitrobenzyl alcohol 
• 121-92-6 3-nitrobenzoic acid 
• 552-16-9 ortho-nitrobenzoic acid 
• 612-25-9 2-Nitrobenzyl alcohol 
• 619-73-8 4-nitrobenzyl chloride 
• 62-23-7 4-nitro-benzoic acid 

Relevant articles and documents

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Iridium-Catalyzed Asymmetric Hydroalkenylation of Norbornene Derivatives

Transition-metal-catalyzed asymmetric hydroalkenylation of alkenes provides an atom-economical method to build molecular complexity from easily available materials. Herein we report an iridium-catalyzed asymmetric hydroalkenylation of unconjugated alkenes with acrylamides and acrylates. The catalytic hydroalkenylation of norbornene derivatives occurred to form products with allylic stereocenters with high chemo-, regio-, and stereoselectivities. DFT calculations revealed that the migratory insertion is irreversible and the enantiodetermination step.

Unprecedented Sequence Control and Sequence-Driven Properties in a Series of AB-Alternating Copolymers Consisting Solely of Acrylamide Units

Herein, we report a method to synthesize a series of alternating copolymers that consist exclusively of acrylamide units. Crucial to realizing this polymer synthesis is the design of a divinyl monomer that contains acrylate and acrylamide moieties connected by two activated ester bonds. This design, which is based on the reactivity ratio of the embedded vinyl groups, allows a “selective” cyclopolymerization, wherein the intramolecular and intermolecular propagation are repeated alternately under dilute conditions. The addition of an amine to the resulting cyclopolymers afforded two different acryl amide units, i.e., an amine-substituted acryl amide and a 2-hydroxy-ethyl-substituted acryl amide in alternating sequence. Using this method, we could furnish ten types of alternating copolymers; some of these exhibit unique properties in solution and in the bulk, which are different from those of the corresponding random copolymers, and we attributed the differences to the alternating sequence.

SYSTEMS AND METHODS FOR INTRACELLULAR DELIVERY VIA NON-CHARGED SEQUENCE-DEFINED CELL-PENETRATING OLIGOMERS

The present disclosure provides oligoTEAs and methods of using the oligoTEAs. The oligoTEAs may be functionalized with one or more cargo group. The oligoTEAs may be made by iterative thiol-ene and Michael reactions. The oligoTEAs functionalized with one or more cargo group may be used to treat bacterial infections, cancers, viral infections, urinary tract infections, skin infections, cystic fibrosis, sepsis, fungal infections, or a combination thereof.