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2-((2-(2-(DIMETHYLAMINO)ETHOXY)ETHYL) METHYLAMINO)ETHANOL, 97 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83016-70-0

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83016-70-0 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 83016-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,1 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83016-70:
(7*8)+(6*3)+(5*0)+(4*1)+(3*6)+(2*7)+(1*0)=110
110 % 10 = 0
So 83016-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H22N2O2/c1-10(2)5-8-13-9-6-11(3)4-7-12/h12H,4-9H2,1-3H3

83016-70-0 Well-known Company Product Price

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  • TCI America

  • (T1598)  N,N,N'-Trimethyl-N'-(2-hydroxyethyl)bis(2-aminoethyl) Ether  >98.0%(GC)(T)

  • 83016-70-0

  • 25mL

  • 290.00CNY

  • Detail
  • TCI America

  • (T1598)  N,N,N'-Trimethyl-N'-(2-hydroxyethyl)bis(2-aminoethyl) Ether  >98.0%(GC)(T)

  • 83016-70-0

  • 500mL

  • 2,450.00CNY

  • Detail

83016-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-(dimethylamino)ethoxy]ethyl-methylamino]ethanol

1.2 Other means of identification

Product number -
Other names NCUPDIHWMQEDPR-UHFFFAOYSA

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:83016-70-0 SDS

83016-70-0Downstream Products

83016-70-0Relevant academic research and scientific papers

Synthesis method of N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether

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Paragraph 0021; 0023-0024, (2021/06/12)

The invention provides a synthesis method of N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether. The synthesis of the N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether comprises the following steps of firstly adding Tos- to dimethylaminoethoxyethanol, and then carrying out substitution reaction on the dimethylaminoethoxyethanol and N-methylethanolamine. The method has the advantages of few by-products, small safety risk, simple operation, high product yield and purity, and small amount of three wastes, and has excellent economic and environmental protection benefits.

Synthesis method of N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether

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Paragraph 0035; 0054-0056; 0058; 0060; 0062; 0064; 0078, (2018/08/04)

The invention discloses a synthesis method of N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether. The synthesis method comprises the following steps of: in a solvent I, adopting dimethylaminoethoxyethanol as a raw material, and under a catalytic system of 2, 2, 6, 6-tetramethyl piperidinoxide-FeCl3-tertbutyl nitrite, utilizing oxygen gas to oxidize the dimethylaminoethoxyethanol into 2-[2-(dimethylamino)ethoxy]acetaldehyde; in a solvent II, mixing N-methylethanolamine with the 2-[2-(dimethylamino) ethoxy]acetaldehyde, adopting Raney Ni as a catalyst, adopting the above mixture as a reactionsystem to carry out hydrogenation and amination, and preparing the N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether. The N, N, N'-trimethyl-N'-hydroxyethyl diaminoethyl ether synthesized by adopting the synthesis method has the characteristics of simple process, low cost, high yield and less pollution.

Preparation method of N,N,N'-trimethyl-N'-hydroxyethyl diaminoethyl ether

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Paragraph 0067; 0068; 0070; 0072-0074; 0076; 0078-0079; 0085, (2018/07/30)

The invention discloses a preparation method of N,N,N'-trimethyl-N'-hydroxyethyl diaminoethyl ether. The preparation method comprises the following steps: 1) in a solvent I, sequentially performing nucleophilic substitution and hydrolysis on N, N-dimethylethanolamine and chloroacetaldehyde dimethyl acetal which serve as raw materials to obtain 2-[2-(dimethylamino)ethyoxyl]acetaldehyde serving as an intermediate product; and 2) in a solvent II, mixing N-methylethanolamine and the 2-[2-(dimethylamino)ethyoxyl]acetaldehyde, performing hydrogenation amination on the mixture serving as a reaction system by taking Raney Ni as a catalyst to prepare the N,N,N'-trimethyl-N'-hydroxyethyl diaminoethyl ether. The N,N,N'-trimethyl-N'-hydroxyethyl diaminoethyl ether prepared by the method has the characteristics of simple process, low cost, high yield and low pollution.

Preparation method for series of polyurethane catalysts

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Paragraph 0059; 0060; 0065, (2016/10/10)

The invention discloses a preparation method for a series of polyurethane catalysts. The preparation method comprises the following steps: SioO2 and Al2O3 with different ratios are employed as carriers, soaked in an ammonium sulfate aqueous solution, dried and roasted, and a silicon-aluminum-loaded solid acid catalyst is prepared; then a mixture of N,N-dimethyl ethanolamine and N-methyl diethanolamine is employed as a raw material, the raw materials and the silicon-aluminum-loaded solid acid catalyst accounting for 1-10% of the total weight of the raw material are added in an autoclave and a reaction is carried out; the filtrate after the reaction is subjected to rectification separation and therefore N-methyl morpholine, 2-dimethylaminoethyl ether and N,N,N'-trimethyl-N'-hydroxyethyl-bis-amino ethyl ether are obtained respectively.

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