Nonylamine

Base Information

• Chemical Name: Nonylamine
• CAS No.: 112-20-9
• Molecular Formula: C9H21N
• Molecular Weight: 143.272
• Hs Code.: 2921 19 99
• European Community (EC) Number: 203-945-9
• UNII: 7L7H2HT4OK
• DSSTox Substance ID: DTXSID7021944
• Nikkaji Number: J96.512J
• Wikidata: Q5649582
• Mol file: 112-20-9.mol

Synonyms:1-nonylamine;1-nonylamine hydrobromide;1-nonylamine hydrochloride;1-nonylamine sulfate (2:1)

Chemical Property of Nonylamine

Chemical Property:

• Appearance/Colour: clear colourless to slightly yellow liquid
• Vapor Pressure: 0.314mmHg at 25°C
• Melting Point: -1 °C
• Refractive Index: n20/D 1.433(lit.)
• Boiling Point: 201.1 °C at 760 mmHg
• PKA: 10.64(at 25℃)
• Flash Point: 62.8 °C
• PSA: 26.02000
• Density: 0.792 g/cm³
• LogP: 3.39600
• Storage Temp.: Store below +30°C.
• Sensitive.: Air Sensitive
• Water Solubility.: Slightly soluble in water.
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 143.167399674
• Heavy Atom Count: 10
• Complexity: 52.7

Purity/Quality:

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

Nonylamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C,N
• Statements: 34-50/53-20/21/22
• Safety Statements: 26-36/37/39-45-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Nitrogen Compounds -> Amines, Aliphatic
• Canonical SMILES: CCCCCCCCCN
• Uses: 1-Nonylamine is used as pharmaceutical intermediate. It is also used as a building block.

Technology Process of Nonylamine

There total 33 articles about Nonylamine 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: 98.0%

nonanonitrile (2243-27-8) → n-Nonylamin (112-20-9)

Guidance literature:

With hydrogen; In water; at 90 ℃; for 4.5h; under 15001.5 Torr;

Reference yield: 88.0%

1-azidononane (80077-60-7) → n-Nonylamin (112-20-9)

Guidance literature:

With hydrogenchloride; indium; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield: 87.0%

2-nonylisoindoline-1,3-dione (82181-90-6) → n-Nonylamin (112-20-9)

Guidance literature:

With hydrazine hydrate; In ethanol; at 80 ℃;

DOI:10.1021/acs.orglett.0c03006

upstream raw materials:

cis-9-octadecenoamide

cis-Octadecenoic acid

1-Chlorononane

1-nitrononane

Downstream raw materials:

1-nonylpyrrolidine-2,5-dione

caprylnitrile

N-nonylbenzamide

N-nonylcyclohexanamine

Refernces

• 1、 Malanga, Corrado,Urso, Andrea,Lardicci, Luciano. "Mercuration demercuration of aliphatic isocyanates: A new mild route to primary amines". . p. 8859 - 8860. Retrieved 1995.
• 2、 Formenti, Dario,Mocci, Rita,Atia, Hanan,Dastgir, Sarim,Anwar, Muhammad,Bachmann, Stephan,Scalone, Michelangelo,Junge, Kathrin,Beller, Matthias. "A State-of-the-Art Heterogeneous Catalyst for Efficient and General Nitrile Hydrogenation". supporting information. p. 15589 - 15595. Retrieved 2020/10/02.
• 3、 -. "Method for preparing primary amine by catalyzing reductive amination of aldehyde ketone compounds". Paragraph 0027-0030; 0051-0055. . Retrieved 2020/05/30.