124-21-0

Basic information

• Product Name: BIS(2-ETHOXYETHYL)AMINE
• Synonyms: 2,2'-DIETHOXYDIETHYLAMINE;BIS(2-ETHOXYETHYL)AMINE;Bisethoxyethylamine;N,N-Bis(2-ethoxyethyl)amine
• CAS NO: 124-21-0
• Molecular Formula: C₈H₁₉NO₂
• Molecular Weight: 161.24
• Mol File: 124-21-0.mol

Chemical Properties

• Melting Point: -50°C
• Boiling Point: 200 °C
• Appearance: /
• Density: 0.89
• Refractive Index: 1.4200-1.4230
• PKA: 8.62±0.19(Predicted)
• CAS DataBase Reference: BIS(2-ETHOXYETHYL)AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(2-ETHOXYETHYL)AMINE(124-21-0)
• EPA Substance Registry System: BIS(2-ETHOXYETHYL)AMINE(124-21-0)

Safety Data

• RIDADR: 2735
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 124-21-0(Hazardous Substances Data)

Usage

Uses

Used in Paint and Coatings Industry:
BIS(2-ETHOXYETHYL)AMINE is used as a solvent to facilitate the application and drying process of paints and coatings, enhancing their performance and durability.
Used in Epoxy Resin Production:
In the production of epoxy resins, BIS(2-ETHOXYETHYL)AMINE acts as a reactive diluent, improving the flow and curing properties of the resin, which is crucial for various applications such as adhesives and composite materials.
Used in Pharmaceutical Production:
BIS(2-ETHOXYETHYL)AMINE is utilized as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Surfactant Production:
As a component in the production of surfactants, BIS(2-ETHOXYETHYL)AMINE helps create products with improved solubility and emulsifying properties, which are essential in cleaning and personal care products.
Used in Agricultural Chemicals:
BIS(2-ETHOXYETHYL)AMINE is used as an intermediate in the formulation of agricultural chemicals, including pesticides and fertilizers, to enhance their effectiveness and application in crop protection and yield improvement.
It is important to adhere to safety precautions and handling guidelines when using BIS(2-ETHOXYETHYL)AMINE to minimize the risks of potential health hazards associated with its moderate hazard classification.

Upstream product

• 139474-24-1 N,N-bis-(2-ethoxy-ethyl)-aniline 
• 288852-82-4 N-benzyl-2-ethoxy-N-(2-ethoxyethyl)ethanamine 
• 13985-50-7 diethanolamine divinyl ether 
• 110-76-9 2-ethoxy-1-ethanamine 
• 628-34-2 2-chloroethyl ethyl ether 
• 110-80-5 2-ethoxy-ethanol 

Downstream Products

• 288852-83-5 3-{[bis-(2-ethoxy-ethyl)-amino]-methyl}-2-hydroxy-5-nitro-benzaldehyde 
• 879098-00-7 C₃₀H₄₄N₂O₆S₂ 
• 1224595-21-4 C₂₄H₃₁FN₂O₆ 
• 1227262-26-1 C₂₅H₃₁N₅O₆S 
• 1386979-36-7 3-({2-[bis-(2-ethoxy-ethyl)-amino]-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl}-amino)-4-chloro-benzoic acid methyl ester 
• 37750-85-9 4,4'-Bis-[N-methyl-N,N-bis-(2-aethoxy-aethyl)-ammonioacetyl]-biphenyl-dibromid 
• 57313-43-6 1.4-Bis-[N-methyl-N_.N-bis-(2-aethoxy-aethyl)-ammonioacetyl]-benzol-dibromid 
• 57313-45-8 [N-Methyl-N_.N-bis-(2-aethoxy-aethyl)-ammonioacetyl]-benzol-bromid 
• 89937-32-6 Bis-(2-ethoxy-ethyl)-(6-{N'-[1-phenyl-meth-(E)-ylidene]-hydrazino}-pyridazin-3-yl)-amine 

Relevant articles and documents

Benzothiazole derivatives with activity as adenosine receptor ligands

The present invention relates to substituted benzothiazole derivitives and to their pharmaceutically acceptable salts useful for the treatment of diseases related to the adenosine receptor.

Synthesis and Photochromism of Crowned Spirobenzothiapyran: Facilitated Photoisomerization by Cooperative Complexation of Crown Ether and Thiophenolate Moieties with Metal Ions

Spirobenzothiapyrans bearing monoaza-12-crown-4, -15-crown-5, -18-crown-6, and oligooxyethylene moieties were synthesized, and their photochromism was examined in the presence of cations in acetonitrile. The cation complexation by their crown ether moieties cannot induce thermal isomerization to their corresponding colored merocyanine form, unlike the corresponding spirobenzopyran derivatives. The UV-light-induced isomerization was, however, facilitated by the cation complexation of the crown ether moieties and the affinity of the merocyanine thiophenolate anion to metal ions, especially in the presence of Li+ and Ag+. The presence of Ag+ brought about the most remarkable effect in the facilitation of photoisomerization of the spirobenzothiapyrans and the thermal stability of the colored merocyanine form mainly due to the powerful interaction of the thiophenolate anion with the soft metal ion.