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59178-93-7

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59178-93-7 Usage

Description

11-(Methacryloylamino)undecanoic acid is a synthetic chemical compound characterized by a unique structure that features a long carbon chain and a reactive methacryloyl group. 11-(METHACRYLOYLAMINO)UNDECANOIC ACID is not naturally occurring and is primarily utilized in the polymer industry. Its carboxyl group allows for chemical modifications, making it versatile for various applications. Due to its properties, it can enhance the flexibility and toughness of products, and it requires special methods for safe and effective production, handling, and use. It is crucial to implement safety measures when working with this chemical, as its impact on human health and the environment is not completely understood.

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)

59178-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-(2-methylprop-2-enoylamino)undecanoic acid

1.2 Other means of identification

Product number -
Other names N-methacryloyl-11-aminoundecanoic acid

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:59178-93-7 SDS

59178-93-7Downstream Products

59178-93-7Relevant articles and documents

Shibayev et al.

, p. 94,95 (1978)

Hydrophilic, hydrophobic, and thermoreversible saccharide gels and forms, and methods for producing same

-

, (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.

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