3-Aminobutanamide

Base Information

• Chemical Name: 3-Aminobutanamide
• CAS No.: 5959-32-0
• Molecular Formula: C4H10N2O
• Molecular Weight: 102.136
• DSSTox Substance ID: DTXSID20448667

Synonyms:3-aminobutanamide;5959-32-0;Butanamide, 3-amino-;Butyramide, 3-amino-;beta-aminobutyric acid amide;SCHEMBL638004;DTXSID20448667;OTVXVVYHNZUDSN-UHFFFAOYSA-N;AKOS005359740;EN300-84785;Z594220690

Chemical Property of 3-Aminobutanamide

Chemical Property:

• XLogP3: -1.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 102.079312947
• Heavy Atom Count: 7
• Complexity: 72.1

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CC(=O)N)N

Technology Process of 3-Aminobutanamide

There total 2 articles about 3-Aminobutanamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethanol (64-17-5) + ammonia (7664-41-7) + ethyl (E)-crotonate (623-70-1) → 2-carbamoyl-1-methylethylamine (5959-32-0) + 3-aminobutanoic acid ethyl ester (5303-65-1) + DL-3.3'-iminodibutyric acid diethyl ester (91694-69-8)

Guidance literature:

at 25 ℃;

Reference yield:

ammonia (7664-41-7) + ethyl (E)-crotonate (623-70-1) → 2-carbamoyl-1-methylethylamine (5959-32-0) + 3-aminobutanoic acid ethyl ester (5303-65-1) + DL-3.3'-iminodibutyric acid diethyl ester (91694-69-8) + 2,4,6-trimethyl-hexahydro-[1,3,5]triazine; trihydrate (58052-80-5,76231-37-3)

Guidance literature:

Raumtemperatur oder erhoehte Temperatur, Produkt 5:oxamidsaeures Ammonium, Produkt 6: Crotonsaeure-amid;

Reference yield:

2-carbamoyl-1-methylethylamine (5959-32-0) → 3-aminobutyric acid (2835-82-7)

Guidance literature:

With lead oxide hydrate; water;

upstream raw materials:

ethanol

ammonia

ethyl (E)-crotonate

Downstream raw materials:

3-aminobutyric acid

((E)-2-{4-[3-(2-Carbamoyl-1-methyl-ethylamino)-2-hydroxy-propoxy]-phenyl}-vinyl)-carbamic acid methyl ester

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