Butylaminoazanium;chloride

Base Information

• Chemical Name: Butylaminoazanium;chloride
• CAS No.: 56795-65-4
• Molecular Formula: C4H12 N2 . Cl H
• Molecular Weight: 124.64
• Mol file: 56795-65-4.mol

Synonyms:

Chemical Property of Butylaminoazanium;chloride

Chemical Property:

• Vapor Pressure: 3.5mmHg at 25°C
• Melting Point: 149-154℃
• Boiling Point: 152.4°Cat760mmHg
• Flash Point: 48.6°C
• PSA: 38.05000
• Density: 0.823g/cm³
• LogP: 2.14300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 124.0767261
• Heavy Atom Count: 7
• Complexity: 21.5

Purity/Quality:

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

ButylhydrazineHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCN[NH3+].[Cl-]
• Uses: Butylhydrazine can be used in the refining of hydrocarbon gases for removal of trace aldehydes.

Technology Process of Butylaminoazanium;chloride

There total 3 articles about Butylaminoazanium;chloride 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: 92.0%

N'-butylhydrazinecarboxylic acid tert-butyl ester (149268-06-4) → N-butylhydrazine monohydrochloride (56795-65-4,70629-61-7)

Guidance literature:

With hydrogenchloride; water; In 1,4-dioxane; at 20 ℃; for 16h;

Reference yield: 80.0%

C10H23N4(1+)*I(1-) → N-butylhydrazine monohydrochloride (56795-65-4,70629-61-7)

Guidance literature:

With hydrogenchloride; potassium hydroxide; 1) reflux;

Reference yield:

→ N-butylhydrazine monohydrochloride (56795-65-4,70629-61-7)

Guidance literature:

With hydrogenchloride; In dichloromethane; at 20 ℃; for 4h;

upstream raw materials:

N'-butylhydrazinecarboxylic acid tert-butyl ester

Downstream raw materials:

butyl-N-benzoylhydrazine

L-butoxycarbonylhydrazine

1-butyl-3-methyl-1H-pyrazol-5-amine

Refernces

• 1、 -. "5-ARYL-4,5-DIHYDRO-(1H)-PYRAZOLINES AS CANNABINOID CB1 RECEPTOR AGONISTS". Page/Page column 13. . Retrieved 2009/04/24.