59178-93-7 Usage
Uses
Used in the Polymer Industry:
11-(Methacryloylamino)undecanoic acid is used as a monomer for the creation of polymers, leveraging its reactive methacryloyl group. This application is due to its ability to improve the flexibility and toughness of the resulting polymers, making them suitable for a wide range of uses.
Used in Chemical Modifications:
The carboxyl group present in 11-(Methacryloylamino)undecanoic acid makes it a candidate for chemical alterations, which can be employed to tailor its properties for specific applications. This versatility allows it to be used in a broad spectrum of industries and applications where customized chemical properties are required.
Used in Product Development:
Due to its ability to enhance the flexibility and toughness of products, 11-(Methacryloylamino)undecanoic acid is used in the development of materials that require these properties. This can include applications in various industries such as automotive, aerospace, and consumer goods, where materials with improved mechanical properties are essential.
Check Digit Verification of cas no
The CAS Registry Mumber 59178-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,7 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59178-93:
(7*5)+(6*9)+(5*1)+(4*7)+(3*8)+(2*9)+(1*3)=167
167 % 10 = 7
So 59178-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H27NO3/c1-13(2)15(19)16-12-10-8-6-4-3-5-7-9-11-14(17)18/h1,3-12H2,2H3,(H,16,19)(H,17,18)
59178-93-7Relevant academic research and scientific papers
FLUORIDE-RELEASING COMPOSITIONS
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Page/Page column 26-27, (2008/12/08)
Chelating monomers and fluoride-releasing compositions are disclosed that may be incorporated into dental composite restorative materials, dental bonding agents or other dental materials, to produce materials with high fluoride release rates, and high fluoride recharge capability. Such dental restorative materials may help reduce the level of dental caries in patients, particularly the level of caries occurring on the margins of the restorative materials.
Hydrophilic, hydrophobic, and thermoreversible saccharide gels and forms, and methods for producing same
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, (2008/06/13)
Polymerizable saccharide monomers are made by the reaction of a saccharose and a (meth)acrylate. Hydrophilic, hydrophobic and thermoreversible gels and foams are formed upon polymerization of the saccharide monomers. Hydrophilic sucrose monomers are synthesized by reaction of sucrose with an epoxy acrylate. Hydrophobic sucrose monomers are synthesized by reaction of sucrose with methacrylol chloride followed by acetyl chloride. Thermoreversible sucrose monomers are obtained by modifying sucrose with polymerizable substituents prepared from methacryloyl chloride and aminocarboxylic acids. The modified sucrose monomers are copolymerized with hydrophobic poly(alkyleneoxide) (meth)acrylates to produce hydrogels exhibiting inverse thermoreversible properties. The thermosensitive hydrogels are biodegradable and can be used in the area of controlled drug delivery.
