93820-37-2

Basic information

• Product Name: (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate
• Synonyms: (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate
• CAS NO: 93820-37-2
• Molecular Formula: C₆H₁₃NO₂
• Molecular Weight: 820.30082
• EINECS: 298-615-4
• Mol File: 93820-37-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate(CAS DataBase Reference)
• NIST Chemistry Reference: (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate(93820-37-2)
• EPA Substance Registry System: (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate(93820-37-2)

Safety Data

• Hazardous Substances Data: 93820-37-2(Hazardous Substances Data)

Usage

General Description

The chemical (2-hydroxyethyl)methyl[3-[(1-oxoisooctadecyl)amino]propyl][2-[(1-oxoisooctadecyl)amino]ethyl]ammonium methyl sulphate is a quaternary ammonium compound commonly used in hair care products, fabric softeners, and industrial applications as a surfactant and antistatic agent. It is a cationic surfactant that is derived from fatty acids and has the ability to neutralize static charges on surfaces. It also has antimicrobial properties and is used as a preservative in personal care products. However, it is important to note that this chemical can be toxic if ingested or inhaled in large quantities and should be handled with care.

Upstream product

• 67-63-0 isopropyl alcohol 
• 109-90-0 ethyl isocyanate 
• 75-04-7 ethylamine 
• 74305-11-6 C₅H₁₀N₂O₄ 

Relevant articles and documents

Removal of flotation collector O-isopropyl-N-ethylthionocarbamate from wastewater

Flotation collector O-isopropyl N-ethylthionocarbamate (IPETC) is widely used for separation of sulfide ores. Its removal from water by several oxidation processes was studied. Photocatalytic oxidation with air in the presence of iron salts, utilizing solar irradiation or artificial UV-A light is very efficient. Oxidation leads through the formation of O-isopropyl N-ethylcarbamate and several other reaction intermediates to total decomposition of organic compound in the final stage in 1 day. Similar results were obtained with a Fenton type oxidation with hydrogen peroxide and iron salts. Treatment with sodium hypochlorite yields mainly O-isopropyl N-ethylcarbamate. The formation of this compound in wastewaters can be of concern, since simple alkyl carbamates are cancer suspect agents.

Nucleophilic Substitutions to Carbonic Acid Derivates. XII. Kinetics and Mechanism of the Reaction of N-Nitro-N-alkyl-urethanes with Primary Aliphatic Amines

The aminolysis of N-alkyl-N-nitrourethanes takes place, as the kinetical studies demonstrate, by means of several consecutive steps.The nucleophilic attack of the amine (first step; reaction B), as well as the proton-transfere (second step; reaction C), are quick pre-equilibres, followed by the slow, rate-determining elimination of the nitramino-group (reaction D).During the deprotonation, an intermediate with two to the nitramino-group antiperiplanar orbitals is formed, providing the necessary mesomeric assistance of the elimination.