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69644-78-6

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69644-78-6 Usage

Description

BIS-ACV, or N,N'-BIS(2-(acetyloxy)ethyl)acrylamide, is a versatile chemical compound known for its role as a crosslinking agent in the manufacturing of polymers and hydrogels. It enhances the structural integrity of materials by forming covalent bonds between polymer chains. Recognized for its biocompatibility, BIS-ACV finds applications in biomedical fields such as drug delivery systems and tissue engineering. Furthermore, it has been explored for potential uses in DNA analysis and other biological research, showcasing its broad utility across different industries.

Uses

Used in Polymer and Hydrogel Manufacturing:
BIS-ACV is used as a crosslinking agent for strengthening the structure of polymers and hydrogels by forming covalent bonds between polymer chains, which improves the material's stability and performance.
Used in Biomedical Applications:
In the biomedical industry, BIS-ACV is used as a component in drug delivery systems to enhance the controlled release of therapeutic agents, and in tissue engineering to support the growth and development of artificial tissues.
Used in DNA Analysis and Biological Research:
BIS-ACV is utilized in DNA analysis and other biological research applications, where its chemical properties contribute to advancements in understanding and manipulating biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 69644-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,4 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69644-78:
(7*6)+(6*9)+(5*6)+(4*4)+(3*4)+(2*7)+(1*8)=176
176 % 10 = 6
So 69644-78-6 is a valid CAS Registry Number.

69644-78-6Relevant articles and documents

EFFICIENT ROUTES TO THE ARNSTEINS'S TRIPEPTIDE δ-(L-α-AMINOADIPYL)-L-CYSTEINYL-D-VALINE (LLD ACV) FROM THE OXIDATION PRODUCTS OF L-LYSINE DERIVATIVES

Liberek, Bogdan,Kasprzykowska, Regina,Wisniewski, Kazimierz

, p. 2857 - 2862 (2007/10/02)

Two efficient syntheses of the linear tripeptide precursor of penam and cephem antibiotics are presented.The routes are characterised by the use of L-lysine derivatives, Z-L-Lys(Z)-OH and H-L-Lys(Z)-OH as starting materials.By the permanganate oxidation t

Synthesis of δ-(L-α-Aminoadipyl)-L-cysteinyl-D-valine and δ-(L-α-Aminoadipyl)-L-cysteinyl-D-valylglycine

Thomson, Gordon A.,Scott, A. Ian,Baxter, Robert L.

, p. 941 - 944 (2007/10/02)

An efficient synthesis of δ-(L-α-aminoadipyl)-L-cysteinyl-D-valine (ACV; 1) and δ-(L-α-aminoadipyl)-L-cysteinyl-D-valylglycine (ACVG; 2) via the protected tripeptide N-benzyloxycarbonyl-1-(p-nitrobenzyl)-δ-(L-α-aminoadipyl)-S-benzyl-L-cysteinyl-D-valine,

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