2997-01-5

Usage

Chemical Properties

Clear colorless liquid

Flammability and Explosibility

Notclassified

Upstream product

• 3386-87-6 1,2-bis-(2-cyanoethoxy)ethane 
• 7440-48-4 cobalt 
• 61515-41-1 3-(2-chloroethanesulfonyl)propionyl chloride 

Downstream Products

• 247210-59-9 C₂₂H₃₂N₂O₆S₂ 
• 247210-62-4 8-(toluene-4-sulfonyl)-1,4-dioxa-8,11-diaza-cyclotetradecane 
• 247210-60-2 8,11-bis-(toluene-4-sulfonyl)-1,4-dioxa-8,11-diaza-cyclotetradecane 
• 247210-64-6 C₄₂H₆₂N₄O₈S₂ 
• 409316-44-5 3,3'-Bis--glykoldipropylether 
• 275823-77-3 tert-butyl N-[3-[2-(3-aminopropoxy)ethoxy]propyl]carbamate 

Relevant academic research and scientific papers

Alkylated aminoether surfactants

This invention provides water-based compositions, particularly coating, ink, and agricultural compositions, manifesting reduced equilibrium and dynamic surface tension by the incorporation of a surface tension reducing amount of certain alkylated aminoether compounds of the structure R—HN(CH2)p[O(CH2)n]mO(CH2)qNH—R′ where n is 2-6, m is 0-4, and p and q are 2-6, and R and R′ independently are an alkyl group comprising 5 to 18 carbons, preferably which is branched or in which the point of attachment to nitrogen is on a nonterminal carbon.

Synthesis of phthalonitrile resins containing ether and imide linkages

Imide-containing phthalonitrile monomers are prepared from a phthalonitrile and an aromatic dianhydride. The monomer and a method for preparing the monomer is disclosed. These monomers are synthesized into heat resistant polymers and copolymers with aromatic ring structure incorporating imide and ether linkages. The synthesis of the high temperature thermosetting polymers and copolymers is also disclosed.

Poly-bis-triazinylimides, their preparation

Poly-bis-triazinylimides of the formula STR1 are prepared from bis-(2,4-dichloro-1,3,5-triazin-6-yl)imides and polyalkylpiperidylamines. They are used as light stabilizers for polymers.

Silicone containing bis-thioether aromatic amines

A silicone containing bis-thioether aromatic amine has a chemical structure wherein an aromatic nucleus at each end of the chemical radical is chemically bonded to the remainder of the chemical radical by either sulfur, sulfoxide or sulfone.

Vinylsulphone hardeners

Vinylsulphone compounds of the general formula wherein x is 1 or 2 and y is 0 or an integer of 1 to 100 are provided. These compounds are useful as cross-linking agents for hydrophilic colloids, especially for gelatin which is in the form of layers of photographic materials.