13205-58-8

Basic information

• Product Name: 2-Nonanamine
• Synonyms: 2-NONYLAMINE;RARECHEM AN KC 0239;(S)-1-Methyloctylamine~(2S)-Nonylamine;2-NONYLAMINE 98%;(2S)-Nonylamine;(S)-1-Methyloctylamine;(S)-(+)-2-AMINONONANE: CHIPROS 99%, EE 99%;(S)-(+)-2-Aminononane, ChiPros 99+%, ee 99+%
• CAS NO: 13205-58-8
• Molecular Formula: C₉H₂₁N
• Molecular Weight: 143.27
• EINECS: -0
• Mol File: 13205-58-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 73°C 19mm
• Flash Point: 71°C
• Appearance: /
• Density: 0,782 g/cm3
• Vapor Pressure: 0.526mmHg at 25°C
• Refractive Index: 1.4271
• PKA: 11.10±0.35(Predicted)
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2-Nonanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nonanamine(13205-58-8)
• EPA Substance Registry System: 2-Nonanamine(13205-58-8)

Safety Data

• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: 2735
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 13205-58-8(Hazardous Substances Data)

Usage

General Description

2-Nonanamine, also known as pelargoniamine, is an organic compound classified as an amine. It consists of a nine-carbon chain with a primary amine functional group at the end. This chemical is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as an intermediate for the production of various products such as lubricants, fuel additives, and surfactants. Furthermore, 2-Nonanamine is utilized in the preparation of rubber chemicals, corrosion inhibitors, and other specialty chemicals. It is important to handle this chemical with caution as it can be irritating to the skin, eyes, and respiratory system, and exposure should be minimized to prevent adverse health effects.

InChI:InChI=1/C9H21N/c1-3-4-5-6-7-8-9(2)10/h9H,3-8,10H2,1-2H3/t9-/m0/s1

Upstream product

• 628-99-9 nonan-2-ol 
• 18197-85-8 α-Nitro-α-methyl-pelargonsaeure-methylester 
• 821-55-6 2-Nonanone 

Downstream Products

• 1011710-71-6 C₁₇H₂₇NO₂ 
• 745783-85-1 2-isocyanatononane 

Relevant articles and documents

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Ambient-Temperature Synthesis of Primary Amines via Reductive Amination of Carbonyl Compounds

Efficient synthesis of primary amines via low-temperature reductive amination of carbonyl compounds using NH3 and H2 as the nitrogen and hydrogen resources is highly desired and challenging in the chemistry community. Herein, we employed naturally occurring phytic acid as a renewable precursor to fabricate titanium phosphate (TiP)-supported Ru nanocatalysts with different reduction degrees of RuO2 (Ru/TiP-x, x represents the reduction temperature) by combining ball milling and molten-salt processes. Very interestingly, the obtained Ru/TiP-100 had good catalytic performance for the reductive amination of carbonyl compounds at ambient temperature, resulting from the synergistic cooperation of the support (TiP) and the Ru/RuO2 with a suitable proportion of Ru0 (52%). Various carbonyl compounds could be efficiently converted into the corresponding primary amines with high yields. More importantly, the conversion of other substrates with reducible groups could also be achieved at ambient temperature. Detailed investigations indicated that the partially reduced Ru and the support (TiP) were indispensable. The high activity and selectivity of Ru/TiP-100 catalyst originates from the relatively high acidity and the suitable electron density of metallic Ru0.

Direct amination of secondary alcohols using ammonia

Hydrogen shuttle: For the first time secondary alcohols and ammonia can be directly converted into primary amines with a selectivity of up to 99% by using a simple ruthenium/phosphine catalyst (see scheme; R1, R2= alkyl, aryl, alkenyl; M=[Ru3(CO)12]; and L=phosphine ligand).