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(2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride is a quaternary ammonium compound with the chemical formula C11H26Cl2N2O5P. It is a phosphonium derivative that features a hydroxyl group, a diazonium group, and a trimethylammonium group within its structure. This versatile chemical is known for its surfactant and antimicrobial properties, making it a valuable ingredient in a range of industrial and commercial products.

61114-50-9

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61114-50-9 Usage

Uses

Used in Disinfectants:
(2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride is used as an antimicrobial agent for disinfectants, where its positively charged ammonium group attracts and binds with negatively charged molecules, effectively neutralizing and eliminating harmful microorganisms.
Used in Hair Care Products:
In the hair care industry, (2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride is used as a surfactant to enhance the cleaning and conditioning properties of hair care products. Its ability to bind with negatively charged molecules helps to remove dirt and oils while maintaining the hair's natural moisture balance.
Used in Fabric Softeners:
(2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride is used as a fabric softener component, providing a positive charge that helps to counteract the negative charges in fabrics, resulting in softer, smoother, and less statically charged textiles.
Used in Antifungal Applications:
The phosphorus-containing moiety of (2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride lends it antifungal properties, making it suitable for use in products designed to prevent and treat fungal infections.
Used in Household and Personal Care Products:
Due to its versatility and effectiveness, (2-[(4-diazoniophenoxy)(hydroxy)phosphoryl]oxyethyl)(trimethyl)ammonium dichloride is widely used across various household and personal care products, including cleaning agents, sanitizers, and cosmetic formulations, where it contributes to improved hygiene and product performance.

Check Digit Verification of cas no

The CAS Registry Mumber 61114-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61114-50:
(7*6)+(6*1)+(5*1)+(4*1)+(3*4)+(2*5)+(1*0)=79
79 % 10 = 9
So 61114-50-9 is a valid CAS Registry Number.

61114-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-diazoniophenoxy)-hydroxyphosphoryl]oxyethyl-trimethylazanium,dichloride

1.2 Other means of identification

Product number -
Other names p-Azophenylphosphorylcholine

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:61114-50-9 SDS

61114-50-9Downstream Products

61114-50-9Relevant academic research and scientific papers

Facile reduction in the synthesis of phosphorylcholine affinity columns

Martin, Lenore M.

, p. 7921 - 7924 (2007/10/03)

Reduction of p-nitrophenylphosphorylcholine to the amine utilizing ammonium formate and 10% Pd/C in methanol, followed by in situ generation of the diazonium salt resulted in the synthesis of p-diazophenylphosphorylcholine. This reaction was simpler than the usual approach utilizing hydrogen gas for the reduction to p-aminophenylphosphorylcholine. The diazonium salt then successfully reacted with the amino acid tyrosine, which had been previously attached to an agarose bead. Alternatively the diazonium salt was coupled to BSA and the resulting conjugate used to coat ELISA plates. Selective PC-binding antibodies recognized the antigen, and bound specifically to both the column and plates.

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