N-Acetylethylenediamine

N-Acetylethylenediamine Basic information
Product Name:N-Acetylethylenediamine
Synonyms:N-ACETYLETHYLENEDIAMINE;Acetamide, N-(2-aminoethyl-);Acetamide, N-(2-aminoethyl)-;N-Monoacetylethylenediamine;N-ACETYLETHYLENEDIAMINE, TECH., 90%;N-AcetylethylenediaMine , 95.0%(GC);N-(2-AMinoethyl)acetaMide, 90% 5GR;2-(Acetamino)ethylamine
CAS:1001-53-2
MF:C4H10N2O
MW:102.14
EINECS:
Product Categories:Intermediates of Dyes and Pigments
Mol File:1001-53-2.mol
N-Acetylethylenediamine Structure
N-Acetylethylenediamine Chemical Properties
Melting point 50 °C (lit.)
Boiling point 128 °C/3 mmHg (lit.)
density 1.066 g/mL at 25 °C (lit.)
refractive index n20/D 1.485(lit.)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka15.97±0.46(Predicted)
color White to Yellow Low-Melting
Sensitive Hygroscopic
BRN 1743120
CAS DataBase Reference1001-53-2(CAS DataBase Reference)
NIST Chemistry ReferenceN-Acetylethylenediamine(1001-53-2)
Safety Information
Risk Statements 34
Safety Statements 23-24/25-36/37/39-26
RIDADR 3259
WGK Germany 3
3
HazardClass 8
PackingGroup III
HS Code 29241990
MSDS Information
ProviderLanguage
N-(2-Aminoethyl)acetamide English
SigmaAldrich English
ALFA English
N-Acetylethylenediamine Usage And Synthesis
Chemical PropertiesWhite to yellow crystalline solid
UsesN-(2-Aminoethyl)acetamide may be used in the preparation of mixed two-component monolayers on glassy carbon. It may be used in the synthesis of lysidine.
General DescriptionN-(2-Aminoethyl)acetamide is an organic building block.
Purification MethodsThe acetyl-diamine has been fractionated under reduced pressure and fraction b 125-130o/5mm was refractionated, fraction b 132-135o/4mm was collected and solidified. It is a low melting hygroscopic solid which can be recrystallised from dioxane/Et2O. It is soluble in H2O, Et2O and *C6H6. The p-toluenesulfonate salt can be recrystallised from EtOH/EtOAc (1:8), has m 125-126o but the free base cannot be recovered from it by basifying and extracting with CH2Cl2. The picrate has m 175o (from EtOH) [Aspinall J Am Chem Soc 63 853 1941, Hall J Am Chem Soc 78 2570 1956]. [Beilstein 4 IV 1193.]
N-ISOPROPYL-2-NITROBENZENESULPHONAMIDE N-Acetyltyramine N-ACETYL-L-PHENYLALANYL-3,5-DIIODO-L-TYROSINE 1,8-I-AEDANS AC-TRP-NH2 N,N,N,N'-tetramethyl-N'-acetylethylenediamine N,N'-DIACETYLETHYLENEDIAMINE TETRAGLYCINE N-ACETYLETHYLENEDIAMINE, [ N-(2-AMINOETHYL)ACETAMIDE ] 2-(2-Aminoethylamino)ethanol 1,5-I-AEDANS H-D-ALA-D-ALA-D-ALA-D-ALA-OH HIPPURYL-HIS-LEU LABOTEST-BB LT00053078 N,N'-(1,2-DIHYDROXYETHYLENE)BISACRYLAMIDE N-ACETYL-ALA-ALA-ALA GLUTATHIONE REDUCED, IMMOBILIZED ON AGAROSE CL-4B AC-TYR-NH2

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