ChemicalBook--->CAS DataBase List--->34730-59-1

34730-59-1

34730-59-1 Structure

34730-59-1 Structure
IdentificationBack Directory
[Name]

sodium 2-[(2-aminoethyl)amino]ethanesulphonate
[CAS]

34730-59-1
[Synonyms]

Vestamin A 95
Sodium 2-((2-aminoethyl)
ethanesulfonate(50% in H2O)
Sodium 5-amino-3-azapentane-1-sulfonate
2-[(2-aminoethyl) amino] sodium sulfonate
Sodium N-(2-aminoethyl)aminoethanesulfonate
sodium 2-[(2-aminoethyl)amino]ethanesulphote
Natrium-2-[(2-aminoethyl)amino]ethansulfonat
SodiuM 2-[(2-aMinoethyl)aMino]ethanesulphona
Sodium 2-((2-aminoethyl)amino)ethanesulfonate
sodium 2-[(2-aminoethyl)amino]ethanesulphonate
N-(2-AMINOETHYL)-3-AMINOETHANESULPHONICACID,SODIUMSALT
2-[(2-AMINOETHYL)AMINO]ETHANE SULFONIC ACID SODIUM SALT
2-[(2-Aminoethyl)amino]ethane-1-sulfonic acid sodium salt
SodiuM 2-((2-aMinoethyl)aMino)ethanesulfonate(50% in H2O)
2-[(2-aminoethyl)amino]-ethanesulfonic acid monosodium salt
Ethanesulfonic acid, 2-(2-aminoethyl)amino-, monosodium salt
sodiuM salt of N-(2-aMinoethyl)-2-aMinoethane sulphonic acid
sodiuM salt of N-(2-aMinoethyl)-2-aMinoethane sulphonic acid (50% in water ) (AAS salt)
[EINECS(EC#)]

252-173-9
[Molecular Formula]

C4H13N2NaO3S
[MDL Number]

MFCD09838703
[MOL File]

34730-59-1.mol
[Molecular Weight]

192.21
Chemical PropertiesBack Directory
[Boiling point ]

106℃[at 101 325 Pa]
[density ]

1.238[at 20℃]
[vapor pressure ]

18hPa at 20℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

5.9[at 20 ℃]
[Appearance]

Colorless to light yellow Liquid
[Water Solubility ]

500mg/L
[InChI]

InChI=1S/C4H12N2O3S.Na.H/c5-1-2-6-3-4-10(7,8)9;;/h6H,1-5H2,(H,7,8,9);;
[InChIKey]

DZMFNPQVBLXJTC-UHFFFAOYSA-N
[SMILES]

C(NCCN)CS(O)(=O)=O.[NaH]
[LogP]

-3.1
[EPA Substance Registry System]

Ethanesulfonic acid, 2-[(2-aminoethyl)amino]-, monosodium salt (34730-59-1)
Safety DataBack Directory
[Symbol(GHS) ]


GHS05
[Signal word ]

Danger
[Hazard statements ]

H318
[Precautionary statements ]

P280-P305+P351+P338-P310
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Chemical Properties]

light yellow liquid
[Uses]

Sodium 2-((2-Aminoethyl)amino)ethanesulfonate is used in the preparation and performance of waterborne polyurethane with ethylenediamine sodium sulfonate as hydrophilic group. Sodium 2-((2-Aminoethyl)amino)ethanesulfonate is also used as crosslinking agent for siloxane coating for transparent plastics.
[Synthesis]

2-(2-Aminoethylamino)ethanol

111-41-1

sodium 2-[(2-aminoethyl)amino]ethanesulphonate

34730-59-1

The general procedure for the synthesis of 2-[(2-aminoethyl)amino]ethanesulfonic acid sodium salt (50% aqueous solution) from hydroxyethyl ethylenediamine was as follows: 5.0 g of β-hydroxyethyl ethylenediamine (1 mol) was placed in a three-necked flask assembled with a stirrer, a thermometer, a dropping funnel, and an ice-salt bath. Concentrated sulfuric acid was slowly added through the dropping funnel while the reaction temperature was maintained below 10 °C using an ice-salt bath during the dropping process until the sulfuric acid addition was complete. After removing the ice-salt bath, the reaction mixture is heated for vacuum distillation until no anhydrous fraction is distilled out to give the intermediate product ethylenediamine ethanol sulfate. Toluene may be added as a water-carrying agent during this process. After the reaction product is cooled to room temperature, sodium carbonate solution is added dropwise until no more gas is produced. Subsequently, a preheated prepared saturated sodium sulfite solution (151 g solute) is added for the sulfonation reaction. The reaction was refluxed at 100 to 120°C for 30 h. Upon completion of the reaction, partial vacuum distillation was carried out, cooled to 90?95°C, and filtered while hot to remove the sodium sulfate and sodium sulfite crystals to obtain the crude sodium salt of ethylenediamine sulfonate. A higher purity sodium salt of ethylenediamine sulfonate can be obtained by subsequent refining processes such as cooling and crystallization, acidification, recrystallization and purification and salting out, with a combined product yield of 75%. It should be noted that the use of concentrated sulfuric acid in this process has high requirements for equipment and produces pollutant gases such as sulfur dioxide; at the same time, due to the need to recrystallize several times to separate the sodium sulfate, a large amount of acid-containing wastewater will be generated.

[References]

[1] Patent: CN106187829, 2016, A. Location in patent: Paragraph 0085; 0086
Spectrum DetailBack Directory
[Spectrum Detail]

sodium 2-[(2-aminoethyl)amino]ethanesulphonate(34730-59-1)1HNMR
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