29508-45-0 Usage
Uses
Used in Industrial Processes:
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as a disinfectant for its ability to eliminate harmful microorganisms, ensuring the safety and cleanliness of various products and environments.
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as a corrosion inhibitor to protect materials from the damaging effects of corrosion, thereby extending their lifespan and maintaining their structural integrity.
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as a catalyst for organic reactions to facilitate and accelerate the process, making it more efficient and cost-effective.
Used in Personal Care Products:
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as a component in personal care products for its surfactant properties, which help to create stable emulsions and improve the texture and performance of these products.
Used in Pesticide Production:
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as an ingredient in the production of pesticides to enhance their effectiveness in controlling pests and ensuring the protection of crops.
Used in Disinfectant Formulations:
DIMETHYLDIETHYLAMMONIUM CHLORIDE is used as a key component in disinfectants for its ability to kill or inactivate pathogens, providing a hygienic environment and preventing the spread of diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 29508-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29508-45:
(7*2)+(6*9)+(5*5)+(4*0)+(3*8)+(2*4)+(1*5)=130
130 % 10 = 0
So 29508-45-0 is a valid CAS Registry Number.
29508-45-0Relevant academic research and scientific papers
Alkylation of ammonium salts catalyzed by imidazolium-based ionic liquid catalysts
Zheng, Zhuo Qun,Wang, Jie,Wu, Ting Hua,Zhou, Xiao Ping
, p. 1095 - 1101 (2008/03/27)
Quaternary ammonium salts were synthesized from ammonium salts and dialkyl carbonates over imidazolium ionic liquid catalysts. The reaction gave almost stoichiometric amounts of the quaternary ammonium salts for halides and nitrates. It was found that the electron-donating property of the alkyl moieties of ammonium cations, the electrophilic nature of the alkyl group of the carbonate, the acidity of the acid that the anion of the ammonium salt corresponds to, and the steric hindrance of the ammonium salts and the dialkyl carbonates are the key factors that influence the yields of quaternary ammonium salts. Strong electron-donating alkyl groups on the nitrogen atom of the ammonium salt, electron-withdrawing groups on the methylene carbon of dialkyl carbonate, and weaker steric hindrance of the starting ammonium salts and dialkyl carbonates favor the alkylation reaction of ammonium salts.
