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Ethylenediamine sulfate, with the molecular formula C2H10N2O4S, is a white crystalline powder that exhibits solubility in water. It is recognized for its chelating and catalytic properties, which make it a valuable component in a variety of industrial processes. Its ability to bind metal ions and enhance the stability and performance of chemical reactions underscores its importance in numerous applications.

22029-36-3

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22029-36-3 Usage

Uses

Used in Adhesives Production:
Ethylenediamine sulfate is used as a chelating agent in the production of adhesives, contributing to the improvement of their stability and performance.
Used in Plastics Industry:
In the plastics industry, ethylenediamine sulfate serves as a catalyst, aiding in the synthesis and processing of various types of plastics.
Used in Textile Industry:
Ethylenediamine sulfate is utilized as a chelating agent in the textile industry, enhancing the dyeing and finishing processes of fabrics.
Used in Dyes Synthesis:
ETHYLENEDIAMINE SULFATE is used as a key intermediate in the synthesis of dyes, ensuring the production of vibrant and stable colorants.
Used in Pharmaceutical Synthesis:
Ethylenediamine sulfate is employed as a reagent in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs.
Used in Agrochemicals Production:
In the agrochemicals sector, ethylenediamine sulfate is used as a catalyst and chelating agent, supporting the production of effective and stable agrochemical products.
Used in Water Treatment:
Ethylenediamine sulfate is used as a chelating agent in water treatment processes, helping to remove metal ions and improve water quality.
Used in Oil Refining:
In the oil refining industry, ethylenediamine sulfate functions as a catalyst, facilitating various chemical reactions that enhance the refining process.
Used in Personal Care Products and Cosmetics Manufacturing:
ETHYLENEDIAMINE SULFATE is used in the formulation of personal care products and cosmetics, where it acts as a chelating agent to improve product stability and performance.
Overall, ethylenediamine sulfate is a versatile chemical compound with a wide range of applications across various industries, from manufacturing to personal care, highlighting its importance in modern industrial chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 22029-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22029-36:
(7*2)+(6*2)+(5*0)+(4*2)+(3*9)+(2*3)+(1*6)=73
73 % 10 = 3
So 22029-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H8N2.H2O4S/c3-1-2-4;1-5(2,3)4/h1-4H2;(H2,1,2,3,4)/p-2

22029-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYLENEDIAMINE SULFATE

1.2 Other means of identification

Product number -
Other names ethylenediammonium sulfate

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:22029-36-3 SDS

22029-36-3Relevant academic research and scientific papers

Gyration and Permittivity of Ethylenediammonium Sulfate Crystals

Nichols, Shane,Martin, Alexander,Choi, Joshua,Kahr, Bart

, p. 460 - 465 (2016)

Ethylenediammonium sulfate (EDS) crystals were grown from aqueous solution and cleaved into thin (100-500 micron) plates. The 422 point group of EDS was confirmed by X-ray diffraction. The constitutive relations of EDS crystals were determined through generalized ellipsometry with an instrument that uses four photoelastic modulators (4PEM). The optical rotation at 500 nm, for example, was + 22.9°/mm along the optic axis and - 12.1°/mm perpendicular to the optic axis for the P41212 crystals. Enantiomorphous twins frequently form across the (001) plane. Mirrored halves must be separated by cleavage in advance of optical measurements. Chirality 28:460-465, 2016.

Onium salts of sulfur-containing oxyanions resulting from reaction of sulfur(IV) oxide with aqueous solutions of 1,2-diamines and morpholine

Khoma,Gel’mbol’dt,Ennan,Baumer,Puzan,Koksharova,Mazepa

, p. 736 - 745 (2017)

Reaction products have been isolated from SO2–L–H2O–О2 systems (L = ethylenediamine, N,N,N′,N′-tetramethylethylenediamine, piperazine, and morpholine) as onium salts [H3NCH2CH2NH3]SO4, [(CH3)2NHCH2CH2NH(CH3)2]SO4, [(CH3)2NHCH2CH2NH(CH3)2]S2O6 ? H2O, [C4H8N2H4]SO3 ? H2O, [C4H8N2H4]S2O6, [C4H8N2H4]SO4 ? H2O, [O(C2H4)2NH2]2SO4 ? H2O. The prepared compounds have been characterized by X-ray diffraction analysis, X-ray powder diffraction, IR and mass spectroscopy.

Four new CuI/AgI-based coordination compounds containing 2-mercapto-5-methyl-1,3,4-thiadiazole: Synthesis, crystal structures and fluorescence properties

Geng, Ying,Jiao, Wei-Zhou,Song, Jiang-Feng,Zhang, Wen,Zhou, Rui-Sha

, (2021)

Effectively constructing CuI/AgI-based coordination polymers containing Hmthd ligands is a challenging work, here, four new coordination compounds [Cu(Hmthd)2Cl]n (1), [Cu3(mthd)2Br]n (2), [Ag(mthd)]n (3) and [Ag2(mthd)I]n (4) have been obtained by reactions of the corresponding metal salts and 2-mercapto-5-methyl-1,3,4-thiadiazole (Hmthd) ligand under solvothermal conditions. All the compounds were fully characterized by single-crystal X-ray diffraction, elemental analysis, IR spectrum, thermalgravimetric analysis and powder X-ray diffraction. Compound 1 is a mononuclear coordination compound, in which two neutral Hmthd molecules and CuCl unit are coplanar. In compound 2, the anionic [CuBr(mthd)]22– units and one-dimensional coplanar cationic {[Cu2(mthd)]+}n chains are connected to each other to form a two-dimensional layered structure. In compound 3, two different one-dimensional puckered [Ag(mthd)]n chains are connected to each other to form a two-dimensional irregular layered structure, in which a (AgS)n chain constructed by staggered Ag3S3 rings is observed. Compound 4 is a two-dimensional double layer coordination framework containing a two-dimensional inorganic (Ag2IS)n double layer. Compound 4 shows the apparent yellow emission with the maximum at 551 nm while exciting at 333 nm, and displays sensitive luminescence quenching response to nitrobenzene with quenching constant (Ksv) of 5.07 × 103 M?1 and detection limit of 5.33 × 10?6 M. This research provides a new strategy to construct the CuI/AgI-based coordination compounds containing Hmthd ligands with extended structures through the synergistic effect of (mthd)- and halide ions.

Structural and spectral characterization of a new non-centrosymmetric organic thiosulfate

Srinivasan, Bikshandarkoil R.,Khandolkar, Savita S.,Jyai, Rita N.,Ravikumar, Krishnan,Sridhar, Balasubramanian,Natarajan, Subramanian

, p. 235 - 241 (2013)

Aqueous reaction of ammonium thiosulfate with ethylenediamine (en) results in the formation of the title compound (enH2)[S2O 3] (1) (enH2 = ethylenediammonium) in good yields. Compound 1 was characterized by analytical data, IR, Raman and NMR spectra, X-ray powder pattern and its crystal structure was determined. The structure of 1 which crystallizes in the non-centrosymmetric orthorhombic space group P2 12121, consists of two crystallographically independent (enH2)2+ dications and two unique thiosulfate anions, which are interlinked by three varieties of H-bonding interactions, namely N-H...O, N-H...S, and C-H...O. 1H and 13C NMR spectra reveal the purity of 1 while its transparent nature can be evidenced from the UV-Vis-NIR spectral data. In compound 1 which exhibits SHG property, the infrared and Raman spectra confirm the presence of the organic dication and the thiosulfate anion.

PROCESS FOR ISOLATION OF AN ORGANIC AMINE

-

Page/Page column 13, (2008/06/13)

The invention relates to a process for the isolation of an organic amine from a composition comprising the organic amine and an acid, or a salt of the organic amine and the acid, wherein the process comprises steps wherein ammonia or hydrazine is added to the composition thereby forming a multi-phase system comprising an organic amine -rich phase and an acid-rich phase, the organic amine-rich phase and the acid-rich phase obtained in step (i) are separated, and the organic amine is isolated from the organic amine -rich phase.

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