18299-54-2

Usage

Uses

Used in Chemical Reactions:
2-Aminoethylammonium chloride is used as a catalyst to facilitate and speed up chemical reactions, enhancing the efficiency and effectiveness of various industrial processes.
Used in Water Treatment:
In the water treatment industry, 2-Aminoethylammonium chloride serves as a corrosion inhibitor, helping to protect infrastructure and equipment from the damaging effects of corrosive substances in water.
Used in Pharmaceuticals and Personal Care Products:
2-Aminoethylammonium chloride is used as an ingredient in certain pharmaceuticals and personal care products, contributing to their formulation and performance.
Used in Cosmetics and Household Products:
2-Aminoethylammonium chloride is used as a surfactant and emulsifying agent in various cosmetic and household products, improving their texture, stability, and effectiveness.
Used in Dietary Supplements:
2-Aminoethylammonium chloride can be found in certain dietary supplements, where it may contribute to the overall health benefits of the product.
Used in Organic Chemical Production:
As a precursor for the production of other organic chemicals, 2-Aminoethylammonium chloride plays a crucial role in the synthesis of a variety of compounds used in different industries.
The safety and regulatory status of 2-Aminoethylammonium chloride are generally well-managed, with various government agencies overseeing its use in consumer products to ensure safety and compliance with industry standards.

InChI:InChI=1/C2H8N2/c3-1-2-4/h1-4H2

Upstream product

• 333-18-6 1,2-diaminoethane dihydrochloride 
• 72138-54-6 N,N′-ethylenebis(3-tert-butylsalicylimine) 
• 107-15-3 ethylenediamine 
• 2565-58-4 chloromethylphosphonic acid 

Downstream Products

• 159928-82-2 N,N,N',N'-tetra(antipyryl-4-methylene)-1,2-ethane-diamine 
• 1852-14-8 ethylene diurea 
• 110-85-0 piperazine 
• 4772-67-2 [(2-{[(cyano)(phenyl)methyl]amino}ethyl)amino](phenyl)acetonitrile 
• 94680-82-7 2,2'-diphenyl-2,2'-ethanediyldiamino-di-propionitrile 
• 81001-99-2 N,N'-ethylenebis(1-phenyl-1,3-propanedione 3-imine) 
• 3403-77-8 N,N'-ethanediyl-bis-propionamide 
• 127282-84-2 Cu(C₆H₄(O)CHNC₂H₄NH₂)2 
• 142-04-1 aniline hydrochloride 
• 14096-51-6 dichloro(ethylenediamine)platinum(II) 
• 3858-78-4 n-butylamine hydrochloride 
• 557-66-4 ethanamine hydrochloride 
• 5470-11-1 hydroxylamine hydrochloride 
• 504-74-5 tetrahydroimidazole 

Relevant academic research and scientific papers

Synthesis method of saccharide-containing polymeric monomer N-(2-D-glucanoamidoethyl)methacrylamide

The invention provides a synthesis method of a saccharide-containing polymeric monomer N-(2-D-glucanoamidoethyl)methacrylamide, and relates to the field of synthesis of organic high molecular materials. The synthesis method comprises the following specific steps: dissolving D-gluconolactone in anhydrous methanol to form a solution, and then sequentially adding intermediates AEMA, triethylamine andhydroquinone into the solution, the ratio of the three components is AEMA: D-glucose lactone: triethylamine = 18: 11: 36, mixing and oscillating for 5 hours to obtain a milky white solution, concentrating through rotary evaporation, repeatedly washing by using anhydrous dichloromethane, performing centrifugal filtration, and performing vacuum drying to obtain a final sample, wherein the ratio ofamounts of substance of the D-gluconolactone and the anhydrous methanol 0.0113:1, and the ratio of amounts of substance of the AEMA, the D-gluconolactone and the triethylamine is 18:11:36. By the synthesis method provided by the invention, the saccharide-containing polymeric monomer which is economical and applicable, can stably exist in a strong acid hydrolysate and can be specifically bonded with and adsorb protein is prepared.

Salen-Based Covalent Organic Framework

The Salen unit represents one of the most important ligands in coordination chemistry. We report herein the first example of a Salen-based covalent organic framework (COF), in which both the construction of the COF structure and the functionalization with Salen moieties have been realized in a single step. Due to its structural uniqueness, the obtained COF material, Salen-COF, possesses high crystallinity and excellent stability. Based on this, a series of metallo-Salen-based COFs were prepared via metalation for further applications.

ORGANOPHOSPHORUS COMPOUNDS AS POTENTIAL FUNGICIDES. PART I. N-(ω-GUANIDINOALKYL)AMINOALKANEPHOSPHONIC ACIDS AND THEIR AMINOPHOSPHONIC PRECURSORS: PREPARATION, NMR SPECTROSCOPY, AND FAST ATOM BOMBARDMENT MASS SPECTROMETRY

N-(ω-Aminoalkyl)- and N-(ω-guanidinoalkyl)-aminoalkanephosphonic acids have been prepared from α,ω-diaminoalkanes by reaction with chloromethanephosphonic acid (or an ester of a halogenoalkanephosphonic acid), followed by treatment with S-methylisothiouronium chloride.Ethylene diamine yielded 1-phosphonomethyl-2-iminoimidazolidine.A number of 1:1 salts of the α,ω-diamines and chloromethanephosphonic acid are also reported.Doubly charged zwitterionic structures are assigned to both ω-amino and ω-guanidino compounds on the basis of 31P and 13C nmr data.Thus the addition of an excess of acid (D2SO4) causes the 31P chemical shift to move to higher field, from ca. 8 to 14 ppm, whilst 1JPC increases from ca. 130 to 150 Hz.The 1H and 13C chemical shifts. of the terminal methylene groups in the polymethylene chain are unaffected by acidification.Fast atom bombardment mass spectrometry gives rise to characteristic + ions, frequently as the base peak, and to fragmentations involving the loss of phosphorous acid, or the formation of ions resulting from carbon-nitrogen or carbon-carbon cleavage.The compounds show activity against a number of fungal pathogens and other microbial organisms.Key words: Organophosphorus; fungicides; guanidinophosphonic acids; aminophosphonic acids; NMR spectroscopy; FAB mass spectrometry.

Oxime carbamates

Novel oxime-carbamates of the formula SPC1 Wherein R1 is --CH3, --CH(CH3)2, EQU1 --C(CH3)3, or --C6 H5 ; R2 is --H or --CH3 ; R3 is --CH3, --CH2 CH3, --(CH2)2 CH3, --(CH2)3 CH3, --CH2 CH2 Cl or --C6 H5 ; R4 is --H, --CH3, --CH2 CH3, --(CH2)2 CH3, --CH(CH3)2, --(CH2)3 CH3, --CH2 CH=CH2, --CH2 C CH, --C6 H5, EQU2 --CH (OH)CCl3, --CH2 CH2 X1, where X1 is --Cl, --Br, --NH2, --OH, --OCOCH3, --OCOCH2 Cl, or --OCONHCH3 ; R5 and R6 are each --H or --CH3, with the proviso that when R5 and R6 are both CH3 then both CH3 groups may be on either the same carbon atom or on different carbon atoms; R7 is H, --CH3 or --CH2 C6 H5 ; X2 is --Cl, --Br or --I; and n is O or 1, with the proviso that when n is 1 then N bears a + charge and X2 bears a - charge. These compounds are useful as insecticides and acaricides.