N-(4-aminobutyl)acetamide hydrochloride

Base Information

• Chemical Name: N-(4-aminobutyl)acetamide hydrochloride
• CAS No.: 18233-70-0
• Molecular Formula: C₆H₁₄N₂O*ClH
• Molecular Weight: 166.651
• Hs Code.: 2924199090
• DSSTox Substance ID: DTXSID00499571
• Mol file: 18233-70-0.mol

Synonyms:18233-70-0;N-(4-aminobutyl)acetamide hydrochloride;N-Acetylputrescine hydrochloride;N-(4-aminobutyl)acetamide;hydrochloride;Acetamide, N-(4-aminobutyl)-, hydrochloride (1:1);MFCD00058264;5-Bromosalicylicacid;Acetamide, N-(4-aminobutyl)-, monohydrochloride;DTXSID00499571;AKOS015950956;N-(4-AMINOBUTYL)ACETAMIDE HCL;s12336;AS-77753;SY347021;HY-113100;CS-0059569;FT-0650845;Acetamide,N-(4-aminobutyl)-,hydrochloride(1:1);N-Acetylputrescine hydrochloride, >=98% (TLC);J-011664;N-(4-Aminobutyl)acetamide--hydrogen chloride (1/1)

Chemical Property of N-(4-aminobutyl)acetamide hydrochloride

Chemical Property:

• Vapor Pressure: 0.000119mmHg at 25°C
• Melting Point: 140-141 °C(Solv: ethanol (64-17-5))
• Boiling Point: 330.6 °C at 760 mmHg
• Flash Point: 153.8 °C
• PSA: 55.12000
• Density: 0.948g/cm3
• LogP: 1.75460
• Storage Temp.: 2-8°C
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 166.0872908
• Heavy Atom Count: 10
• Complexity: 83.1

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-Acetylputrescine hydrochloride ≥98% (TLC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(=O)NCCCCN.Cl

Technology Process of N-(4-aminobutyl)acetamide hydrochloride

There total 1 articles about N-(4-aminobutyl)acetamide hydrochloride 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: 28.0%

acetic anhydride (108-24-7) + 1,4-diaminobutane (110-60-1) → monoacetyl-1,4-diaminobutane hydrochloride (18233-70-0)

Guidance literature:

In acetic acid; at 50 - 60 ℃;

DOI:10.1016/0223-5234(87)90296-0

upstream raw materials:

acetic anhydride

1,4-diaminobutane

Refernces