24304-84-5

Basic information

• Product Name: 2-[(2-AMINOETHYL)THIO]ETHAN-1-OL
• Synonyms: 2-[(2-AMINOETHYL)THIO]ETHAN-1-OL;2-(2-AMINOETHYLTHIO)ETHANOL;2-AMINO-2-HYDROXYDIETHYLSULFIDE;2-amino-2-hydroxydiethylsulphite;2-Aminoethyl-2-hydroxyethyl sulfide;2-Amino-2-hydroxydiethylsulfit;2-[(2-Aminoethyl)thio]ethan-1-ol, 90+%;5-Amino-3-thiapentane-1-ol
• CAS NO: 24304-84-5
• Molecular Formula: C₄H₁₁NOS
• Molecular Weight: 121.2
• EINECS: 246-142-9
• Product Categories: Aliphatics
• Mol File: 24304-84-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 3°C
• Boiling Point: 221°C
• Flash Point: 112.3 °C
• Appearance: /
• Density: 1.104 g/cm³
• Vapor Pressure: 0.00158mmHg at 25°C
• Refractive Index: 1.525
• PKA: pK1: 9.27(+1) (25°C)
• CAS DataBase Reference: 2-[(2-AMINOETHYL)THIO]ETHAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(2-AMINOETHYL)THIO]ETHAN-1-OL(24304-84-5)
• EPA Substance Registry System: 2-[(2-AMINOETHYL)THIO]ETHAN-1-OL(24304-84-5)

Safety Data

• Hazard Codes: C:Corrosive
• Statements: 34
• Safety Statements: 26-36/37/39
• RIDADR: 2735
• Hazardous Substances Data: 24304-84-5(Hazardous Substances Data)

Usage

General Description

2-[(2-Aminoethyl)thio]ethan-1-ol is an organic chemical compound that contains an amino (-NH2) and a hydroxyl (-OH) group and belongs to the class of compounds known as taurines and derivatives. This chemical structure includes a 2-aminoethylthio group that links it to the ethanol. It's noteworthy for its potential uses in various scientific and industrial processes, although specific applications may depend on additional research. As with any chemical, it should be handled with care to prevent unnecessary exposure or accidents caused by improper use. Its properties such as boiling point, molecular weight, solubility, and other characteristics could vary and are important to consider in its applications.

InChI:InChI=1/C4H11NOS/c5-1-3-7-4-2-6/h6H,1-5H2

Upstream product

• 689-98-5 chloroethylamine 
• 60-24-2 2-hydroxyethanethiol 
• 2576-47-8 2-bromoethylamine hydrobromide 
• 870-24-6 2-chloroethanamine hydrochloride 
• 75-21-8 oxirane 
• 60-23-1 Cysteamine 
• 151-56-4 ethyleneimine 

Downstream Products

• 133760-84-6 2-hydroxy-N-(2-ethanolthioethyl)-2-phenyl-ethylamine 
• 95239-79-5 1-(p-Cyanophenyl)-3-triazene 

Relevant articles and documents

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Entrapment of a Pseudo-Tetrahedral CoII Center by Thioether Sulfur Bound {Co2(μ-L)} Fragments: Synthesis, Field-Induced Single-Ion Magnetism and Catechol Oxidase Mimicking Activity

Simultaneous incorporation of both CoII and CoIII ions within a new thioether S-bearing phenol-based ligand system, H3L (2,6-bis-[{2-(2-hydroxyethylthio)ethylimino}methyl]-4-methylphenol) formed [Co5] aggregates [CoIICoIII 4L2(μ-OH)2(μ1,3-O2CCH3)2](ClO4)4?H2O (1) and [CoIICoIII 4L2(μ-OH)2(μ1,3-O2CC2H5)2](ClO4)4?H2O (2). The magnetic studies revealed axial zero-field splitting (ZFS) parameter, D/hc=?23.6 and ?24.3 cm?1, and E/D=0.03 and 0.00, respectively for 1 and 2. Dynamic magnetic data confirmed the complexes as SIMs with Ueff/kB=30 K (1) and 33 K (2), and τ0=9.1×10?8 s (1), and 4.3×10?8 s (2). The larger atomic radius of S compared to N gave rise to less variation in the distortion of tetrahedral geometry around central CoII centers, thus affecting the D and Ueff/kB values. Theoretical studies also support the experimental findings and reveal the origin of the anisotropy parameters. In solutions, both 1 and 2 which produce {CoIII 2(μ-L)} units, display solvent-dependent catechol oxidation behavior toward 3,5-di-tert-butylcatechol in air. The presence of an adjacent CoIII ion tends to assist the electron transfer from the substrate to the metal ion center, enhancing the catalytic oxidation rate.

Has high water washing fastness and bears the friction fastness reactive red dye and the preparation method

The invention discloses a reactive red dye with high washing fastness and rubbing fastness and a preparation method of the reactive red dye. Acetanilide reacts with chlorosulfonic acid and sulfoxide chloride to generate acetylsulfanilyl chloride; acetylsulfanilyl chloride is condensed with a sulfide generate by reacting a 2-chlorethamin hydrochloride with mercaptoethanol to obtain thioether; the thioether is oxidized and esterified to obtain 2-[2-(4-aminobenzenesulfonamido) ethyl sulfuryl] hydroxyethyl sulfate which is primarily condensed with cyanuric chloride and secondarily condensed with H acid to obtain a condensation compound; the condensation compound is cooled and then coupled with the diazonium salt of 1.5 acid under an alkaline condition, and the product is filtered and then the filtrate is collected and is subjected to direct spray drying to obtain a semi-finished product. The reactive red dye has the characteristics of bright color, high solubility high substantivity, high compatibility, high lifting power, high fixation rate, excellent diversified fastness and the like. The reactive red dye is suitable for dyeing, printing and pad dyeing of cellulosic fibers, protein fibers, viscose and polyarmide fibers, and higher than common types in rubbing fastness and washing fastness by 0.5 to 1 level.