Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5442-83-1

N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine is a complex organic compound with the molecular formula C22H37NO2. It is a derivative of ethylamine, featuring a long alkyl chain and a phenoxy group. This chemical is characterized by its two methyl groups attached to the nitrogen atom, a central ethylamine structure, and a bulky 1,1,3,3-tetramethylbutyl group attached to the phenoxy moiety. The compound's structure endows it with unique properties, such as its potential use as a surfactant or in the synthesis of other chemicals. Its specific applications and effects depend on the context in which it is used, and further research may be required to fully understand its behavior and potential uses.

5442-83-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

  • Ethanamine, N,N-dimethyl-2-(2-(4-(1,1,3,3-tetramethylbutyl)phenoxy)ethoxy)-

    Cas No: 5442-83-1

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier
  • 5442-83-1 Structure

  • Basic information

    1. Product Name: N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine
    2. Synonyms: N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine
    3. CAS NO:5442-83-1
    4. Molecular Formula: C20H35NO2
    5. Molecular Weight: 321.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5442-83-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 400.9°C at 760 mmHg
    3. Flash Point: 102.3°C
    4. Appearance: /
    5. Density: 0.939g/cm3
    6. Vapor Pressure: 1.23E-06mmHg at 25°C
    7. Refractive Index: 1.486
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine(5442-83-1)
    12. EPA Substance Registry System: N,N-Dimethyl-2-[2-[p-(1,1,3,3-tetramethylbutyl)phenoxy]ethoxy]ethylamine(5442-83-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5442-83-1(Hazardous Substances Data)

5442-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5442-83-1 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 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5442-83:
(6*5)+(5*4)+(4*4)+(3*2)+(2*8)+(1*3)=91
91 % 10 = 1
So 5442-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H35NO2/c1-19(2,3)16-20(4,5)17-8-10-18(11-9-17)23-15-14-22-13-12-21(6)7/h8-11H,12-16H2,1-7H3

5442-83-1SDS

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 N,N-dimethyl-2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethanamine

1.2 Other means of identification

Product number -
Other names n,n-dimethyl-2-{2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy}ethanamine

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:5442-83-1 SDS

5442-83-1Relevant articles and documents

METHOD FOR PREPARING ARYL POLYOXY ALKYL QUATERNARY AMMONIUM COMPOUND

-

, (2014/03/25)

A method for preparation of an aryl poly(oxalkyl) quaternary ammonium compound is provided, said method comprising steps of: 1) reacting a phenol with a dihalopolyalkylene ether under the action of a phase transfer catalyst, to obtain an arylpoly(oxalkyl) halide; 2) reacting said arylpoly(oxalkyl) halide with an amination reagent under the action of a phase transfer catalyst, to obtain an arylpoly(oxalkyl) amine; 3) reacting said arylpoly(oxalkyl) amine with an alkylation reagent, to obtain an aryl poly(oxalkyl) quaternary ammonium compound; wherein R1 is H or a C1 to C16 alkyl group, located in the ortho, meta or para position; n is an integer of 2 to 6; R2 is H or a C1 to C16 alkyl group; R3 is H or a C1 to C16 alkyl group; R4 is a C1 to C16 alkyl group; X1 is Br or Cl; X is Cl, Br, or I. The preparation method according to the present invention requires low temperature and low pressure, the reaction time is short, and an overall yield can reach 75%. The operation is simple, the cost is low, and the product can be separated easily and have a purity of pharmaceutical grade, thereby facilitating the large-scale production.

METHOD FOR PREPARATION OF ARYL POLY(OXALKYL) QUATERNARY AMMONIUM COMPOUND

-

, (2014/07/08)

A method for preparation of an aryl poly(oxalkyl) quaternary ammonium compound is provided, said method comprising steps of: 1) reacting a phenol with a dihalopolyalkylene ether under the action of a phase transfer catalyst, to obtain an arylpoly(oxalkyl) halide; 2) reacting said arylpoly(oxalkyl) halide with an amination reagent under the action of a phase transfer catalyst, to obtain an arylpoly(oxalkyl) amine; 3) reacting said arylpoly(oxalkyl) amine with an alkylation reagent, to obtain an aryl poly(oxalkyl) quaternary ammonium compound; wherein R1 is H or a C1 to C16 alkyl group, located in the ortho, meta or para position; n is an integer of 2 to 6; R2 is H or a C1 to C16 alkyl group; R3 is H or a C1 to C16 alkyl group; R4 is a C1 to C16 alkyl group; X1 is Br or Cl; X is Cl, Br, or I. The preparation method according to the present invention requires low temperature and low pressure, the reaction time is short, and an overall yield can reach 75%. The operation is simple, the cost is low, and the product can be separated easily and have a purity of pharmaceutical grade, thereby facilitating the large-scale production.

Method for preparing arylpoly(oxyalkyl) amines

-

Page/Page column 4, (2010/11/30)

The invention pertains to a process for preparing an arylpoly(oxyalkyl)compound, wherein the process involves reacting a phenol with a halohydrin, and reacting the reaction product with an amino alkyl halide. The invention seeks to provide a less hazardous alternative to conventional preparation processes where arylpoly(oxyalkyl)compounds are made starting from an extremely toxic and hazardous dihalogeno-polyalkylene ether. The preferred arylpoly(oxyalkyl)compound is benzethonium chloride.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5442-83-1