18299-54-2

Basic information

• Product Name: 2-Aminoethylammonium chloride
• Synonyms: RARECHEM AL BW 1341;2-aminoethylammonium chloride;1,2-ETHANEDIAMINE, MONOHYDROCHLORIDE;ETHYLENEDIAMINEHCL;Ethylenediamine monohydrochloride;Nsc263495;Ethane-1,2-diamine hydrochloride
• CAS NO: 18299-54-2
• Molecular Formula: C₂H₉N₂*Cl
• Molecular Weight: 96.56
• EINECS: 242-181-0
• Mol File: 18299-54-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 143 °C
• Boiling Point: 119.7 °C at 760 mmHg
• Flash Point: 33.9 °C
• Appearance: /
• Density: 1.159 g/cm³
• CAS DataBase Reference: 2-Aminoethylammonium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Aminoethylammonium chloride(18299-54-2)
• EPA Substance Registry System: 2-Aminoethylammonium chloride(18299-54-2)

Safety Data

• Hazardous Substances Data: 18299-54-2(Hazardous Substances Data)

Usage

General Description

2-Aminoethylammonium chloride, also known as monoethanolamine hydrochloride, is a chemical compound with the formula C2H8ClN2. It is a white, crystalline solid at room temperature and is highly soluble in water. 2-Aminoethylammonium chloride has a variety of industrial applications, including as a catalyst in chemical reactions, a corrosion inhibitor in water treatment, and an ingredient in certain pharmaceuticals and personal care products. It is also used as a surfactant and emulsifying agent in various cosmetic and household products. Additionally, it can be found in certain dietary supplements and as a precursor for the production of other organic chemicals. This chemical is generally regarded as safe for use in these applications and is regulated by various government agencies for its use in consumer products.

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

Upstream product

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

Downstream Products

• 504-74-5 tetrahydroimidazole 
• 159928-82-2 N,N,N',N'-tetra(antipyryl-4-methylene)-1,2-ethane-diamine 
• 534-26-9 lysidine 
• 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 
• 65136-87-0 N?(2?aminoethyl)?4?methoxybenzamide 
• 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 

Relevant articles and documents

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.

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.