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Diacrylamide, also known as N,N’-methylenebis(acrylamide), is a white, odorless solid that is highly soluble in water and commonly used as a crosslinking agent in polymerization reactions. It is a key component in the production of polyacrylamide, a versatile polymer with applications across various industries.

20602-80-6

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20602-80-6 Usage

Uses

Used in Polymer Production:
Diacrylamide is used as a crosslinking agent for the production of polyacrylamide, a polymer with diverse applications in industrial, agricultural, and environmental sectors due to its unique properties such as high water absorption, flocculation, and gel formation capabilities.
Used in Gel Electrophoresis:
In the field of molecular biology, diacrylamide is used as a crosslinking agent in the production of gel electrophoresis gels, which are essential for the separation and analysis of proteins and DNA molecules. Its ability to form a stable and uniform gel matrix allows for accurate and reliable separation of biomolecules based on their size and charge.
Used in Water Treatment:
Diacrylamide is utilized in the water treatment industry as a flocculant to remove suspended solids and impurities from water. The high water absorption and flocculation properties of polyacrylamide, which is produced using diacrylamide, make it an effective agent for water purification processes.
Used in Oil Recovery:
In the petroleum industry, diacrylamide is used in the production of polymers that enhance oil recovery. These polymers are injected into oil reservoirs to improve the sweep efficiency and reduce the mobility of oil, thereby increasing the amount of oil that can be extracted.
Used in Paper Manufacturing:
Diacrylamide is employed in the paper manufacturing process to improve the strength and stability of paper products. The crosslinking properties of diaryrlamide help to create a stronger paper structure, making it more resistant to tearing and deformation.
However, it is important to note that diacrylamide is considered a potential human carcinogen and is toxic if ingested, inhaled, or absorbed through the skin. Therefore, proper handling, storage, and disposal measures should be taken to minimize the risk to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 20602-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20602-80:
(7*2)+(6*0)+(5*6)+(4*0)+(3*2)+(2*8)+(1*0)=66
66 % 10 = 6
So 20602-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c1-3-5(8)7-6(9)4-2/h3-4H,1-2H2,(H,7,8,9)

20602-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-prop-2-enoylprop-2-enamide

1.2 Other means of identification

Product number -
Other names acrylamide acrylester

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:20602-80-6 SDS

20602-80-6Upstream product

20602-80-6Downstream Products

20602-80-6Relevant academic research and scientific papers

Nematocide control diacylimide control diacylimide compositions

-

, (2008/06/13)

The invention provides nematocide control diacylimide compositions which include compounds having the formula: STR1 where R and R' are selected from alkyl, alkenyl, haloalkyl and haloalkenyl having from 1-5 carbon atoms, being the same or different groups. The compositions of this invention show excellent agricultural nematocidal activity, and particularly, the control of endoparasitic and ectoparasitic worms, such as the root knot nematocide, which exist in the soil at some stage of their life cycles. The diacylimide compounds generally are prepared by reacting a suitable amide with an acyl halide. The acyl halide precursor may be prepared, if necessary, from the corresponding acid by reaction with a suitable halogenating agent, such as thionyl chloride. Similarly, a given amide may be readily prepared, for example, from the corresponding acyl halide by reaction with ammonia.

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