Isobutylamine Hydrochloride

Base Information

• Chemical Name: Isobutylamine Hydrochloride
• CAS No.: 5041-09-8
• Molecular Formula: C4H11 N . Cl H
• Molecular Weight: 109.599
• Hs Code.: 2921199090
• European Community (EC) Number: 680-199-4
• UNII: K8H0OJB3OI
• DSSTox Substance ID: DTXSID90964667
• Wikidata: Q27282090
• Mol file: 5041-09-8.mol

Synonyms:isobutylamine;isobutylamine hydrochloride

Chemical Property of Isobutylamine Hydrochloride

Chemical Property:

• Vapor Pressure: 144mmHg at 25°C
• Melting Point: 176.0 to 180.0 °C
• Boiling Point: 67.7°C at 760 mmHg
• Flash Point: 25.2°C
• PSA: 26.02000
• LogP: 2.10340
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility.: almost transparency in Water
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 109.0658271
• Heavy Atom Count: 6
• Complexity: 17.6

Purity/Quality:

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

2-Methylpropan-1-amineHydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 36/37/38-41-37/38-22
• Safety Statements: 26-36/37/39-39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)CN.Cl

Technology Process of Isobutylamine Hydrochloride

There total 2 articles about Isobutylamine 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:

tetradecanoic acid N-(2-methylpropyl)amide (74420-88-5) → isobutylamine hydrochloride (5041-09-8) + n-tetradecanoic acid (544-63-8)

Guidance literature:

With hydrogenchloride; In ethanol; for 12h; Heating;

Reference yield:

isobutyl-thiocarbamic acid ; mercury (II)-compound → carbon oxide sulfide (463-58-1) + isobutylamine hydrochloride (5041-09-8) + isobutyl isocyanate (1873-29-6)

Guidance literature:

at 160 - 165 ℃;

Reference yield: 83.0%

isobutylamine hydrochloride (5041-09-8) + saccharin (81-07-2) → N-(1,1-dioxobenzo[d]isothiazol-3-yl)isobutylamine (81038-90-6)

Guidance literature:

With N,N-dimethyl-cyclohexanamine; phosphorus pentoxide; at 240 ℃; for 2h;

upstream raw materials:

tetradecanoic acid N-(2-methylpropyl)amide

Downstream raw materials:

isobutyl isocyanate

isobutyl urea

1-isobutyl-biguanide; hydrochloride

N-Benzolsulfonyl-N'-iso-butyl-carbodiimid, N-iso-Butyliminomethylen-benzolsulfonamid

Refernces