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Tert-Butyl (3-MethacrylaMidopropyl)carbaMate, also known as MABC, is a white crystalline solid that is commonly used as a cross-linking agent in the production of polyurethane resins. It is soluble in organic solvents, has a relatively low volatility, and is considered to be a low-toxicity chemical.

219739-79-4

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219739-79-4 Usage

Uses

Used in Polyurethane Resin Production:
MABC is used as a cross-linking agent to improve the mechanical properties and adhesion of polyurethane resins to various substrates.
Used in Adhesives:
MABC is used as a stabilizer and tackifier in adhesives to enhance their performance and bonding capabilities.
Used in Coatings and Sealants:
MABC is used as a filler in coatings and sealants to improve their physical and chemical properties, such as durability and resistance to environmental factors.
Overall, MABC plays a crucial role in various industries, including plastics, adhesives, coatings, and sealants, by enhancing the performance and properties of the materials in which it is incorporated.

Check Digit Verification of cas no

The CAS Registry Mumber 219739-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,7,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219739-79:
(8*2)+(7*1)+(6*9)+(5*7)+(4*3)+(3*9)+(2*7)+(1*9)=174
174 % 10 = 4
So 219739-79-4 is a valid CAS Registry Number.

219739-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[3-(2-methylprop-2-enoylamino)propyl]carbamate

1.2 Other means of identification

Product number -
Other names -

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:219739-79-4 SDS

219739-79-4Relevant academic research and scientific papers

Photosensitive compound and preparation method and application thereof

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Paragraph 0071; 0089-0091, (2021/06/09)

The invention discloses a photosensitive compound and a preparation method and application thereof, and relates to the technical field of protein nucleic acid co-immobilization, the photosensitive compound is a polyacrylamide compound, and comprises a tetrazole group and a furan group; the compound is prepared from the following raw materials: N-(3-aminopropyl) tert-butyl carbamate, methacryloyl chloride furan-2-yl boric acid, [hydroxyl (phenyl)-lambda 3-iodo] 4-methyl benzene sulfonate and the like. Protein and nucleic acid co-immobilization electrophoresis gel can be prepared, and protein and nucleic acid in single cells or multiple cells can be quantitatively or semi-quantitatively detected; the compound can also be used for microchip electrophoresis mobility analysis, western blotting, nucleic acid blotting hybridization, single-cell western blotting, single-cell northern/source blotting hybridization or capillary electrophoresis western blotting. The protein and nucleic acid co-immobilization gel can be used for simultaneously immobilizing protein and nucleic acid in situ to research the interaction between the protein and DNA (Deoxyribose Nucleic Acid).

COMPOSITIONS AND ASSOCIATED METHODS FOR RADIOISOTOPE-BINDING MICROPARTICLES

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, (2014/09/29)

The present disclosure relates to polymeric materials that may be labeled with a radioisotope, to processes for producing the labeled polymeric material, and to methods of using the materials in analytical and therapeutic applications. Specifically, the disclosure relates to injectable and implantable microparticles, such as microspheres, which are associated with radioisotopes such that the microparticles are both therapeutic and detectable. The radioisotope-containing microparticles are useful for embolization and other therapeutic medical applications.

Photoactivatable nucleic acids

-

, (2008/06/13)

A photoactivatable nucleic acid derivative composition in which one or more photoreactive group(s) are bound to a natural or synthetic nucleic acid. The photoreactive groups can be bound to the nucleic acid before, during or after its formation, and can t

Medicament incorporation matrix

-

, (2008/06/13)

A coating composition, in both its uncrosslinked and crosslinked forms, for use in delivering a medicament from the surface of a medical device positioned in vivo. Once crosslinked, the coating composition provides a gel matrix adapted to contain the medi

Target molecule attachment to surfaces

-

, (2008/06/13)

Method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate. The reagent composition includes groups capable of covalently binding to the target molecule. Optionally, the composition c

PHOTOACTIVATABLE NUCLEIC ACID DERIVATIVES

-

, (2008/06/13)

A photoactivatable nucleic acid derivative composition in which one or more photoreactive group(s) are bound to a natural or synthetic nucleic acid. The photoreactive groups can be bound to the nucleic acid before, during or after its formation, and can t

TARGET MOLECULE ATTACHMENT TO SURFACES

-

, (2008/06/13)

Method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate. The reagent composition includes groups capable of covalently binding to the target molecule. Optionally, the composition c

Reagent and method for attaching target molecules to a surface

-

, (2008/06/13)

Method and reagent composition for covalent attachment of target molecules, such as nucleic acids, onto the surface of a substrate. The reagent composition includes groups capable of attracting the target molecule as well as groups capable of covalently binding to the target molecule, once attracted. Optionally, the composition can contain photoreactive groups for use in attaching the reagent composition to the surface.

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