5444-06-4 Usage
Uses
Used in Personal Care Industry:
(2-(benzoyloxy)ethyl)dimethylammonium chloride is used as a conditioning agent in hair care products for its ability to improve the manageability and texture of hair, providing a smoother and shinier appearance.
Used in Cosmetics Industry:
In the cosmetics industry, (2-(benzoyloxy)ethyl)dimethylammonium chloride is used as an emulsifying agent, which helps to mix and stabilize oil and water components in cosmetic formulations, contributing to the product's stability and performance.
Used in Pharmaceutical Products:
(2-(benzoyloxy)ethyl)dimethylammonium chloride is utilized as an antimicrobial agent in some pharmaceutical products, leveraging its ability to interact with negatively charged microbial cell surfaces, thereby exhibiting antimicrobial properties.
However, it is crucial to handle this chemical with care due to its potential to cause skin and eye irritation, as well as respiratory issues if inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 5444-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5444-06:
(6*5)+(5*4)+(4*4)+(3*4)+(2*0)+(1*6)=84
84 % 10 = 4
So 5444-06-4 is a valid CAS Registry Number.
5444-06-4Relevant articles and documents
Physicochemical parameters involved in the lethal toxicity of N,N-[(dimethylamino)ethyl]-4-substituted benzoate hydrochlorides: A QSAR study
Do Amaral,Oliveira,Neidlein,Gallacci,Caprara,Miyazaki
, p. 433 - 443 (1997)
A set of sixteen para-substituted N,N-[(dimethylamino)ethyl] benzoate hydrochlorides structurally related to procaine was synthesized. The apparent partition coefficients were determined by either shake-flask or HPLC methods and were taken as hydrophobic parameters. The IR stretching frequencies of the carbonyl group were determined in chloroform and taken as one of the electronic parameters. Additional physicochemical parameters were either taken from the literature: π, a, J and R, MR4, or calculated: log P. The lethal potency was determined in the mouse via the LD50. In order to verify the nature and the relative contributions of the physicochemical parameters to lethal toxicity, QSAR equations were derived using regression analysis. A major contribution of hydrophobicity together with a smaller but still significant contribution of electronic or polar properties was found to describe the toxicity within this set of compounds.
