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1-AMINONONANE, also known as 1-Nonylamine, is a clear colorless to slightly yellow liquid with chemical properties that make it a versatile compound in various industries. It is primarily used as a pharmaceutical intermediate and as a building block for the synthesis of other organic compounds.

112-20-9

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112-20-9 Usage

Uses

Used in Pharmaceutical Industry:
1-AMINONONANE is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its chemical properties allow it to be a key component in the development of new pharmaceuticals, contributing to the advancement of medical treatments.
Used in Chemical Industry:
1-AMINONONANE serves as a building block in the chemical industry, where it is used in the synthesis of other organic compounds. Its versatility and reactivity make it a valuable component in the production of various chemical products, including surfactants, detergents, and other specialty chemicals.

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 2392, 1962 DOI: 10.1021/jo01054a026Tetrahedron, 48, p. 4623, 1992 DOI: 10.1016/S0040-4020(01)81236-9Tetrahedron Letters, 36, p. 8859, 1995 DOI: 10.1016/0040-4039(95)01839-A

Hazard

Moderate fire risk. Skin irritant.

Check Digit Verification of cas no

The CAS Registry Mumber 112-20-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112-20:
(5*1)+(4*1)+(3*2)+(2*2)+(1*0)=19
19 % 10 = 9
So 112-20-9 is a valid CAS Registry Number.
InChI:InChI=1/2C9H21N.H2O4S/c2*1-2-3-4-5-6-7-8-9-10;1-5(2,3)4/h2*2-10H2,1H3;(H2,1,2,3,4)

112-20-9 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (A18209)  1-Nonylamine, 97%   

  • 112-20-9

  • 25g

  • 878.0CNY

  • Detail
  • Alfa Aesar

  • (A18209)  1-Nonylamine, 97%   

  • 112-20-9

  • 100g

  • 2912.0CNY

  • Detail
  • Alfa Aesar

  • (A18209)  1-Nonylamine, 97%   

  • 112-20-9

  • 500g

  • 11673.0CNY

  • Detail

112-20-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name nonan-1-amine

1.2 Other means of identification

Product number -
Other names Nonylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112-20-9 SDS

112-20-9Relevant academic research and scientific papers

Mercuration demercuration of aliphatic isocyanates: A new mild route to primary amines

Malanga, Corrado,Urso, Andrea,Lardicci, Luciano

, p. 8859 - 8860 (1995)

Aliphatic isocyanates react with mercury acetate in THF/H2O and successively with sodium boro hydride to give aliphatic primary amines in good yields in short reaction times with high stereo control.

A convenient Hofmann reaction of carboxamides and cyclic imides mediated by trihaloisocyanuric acids

Bastos, Gustavo A.,de Mattos, Marcio C.S.

, (2021/09/29)

A simple, efficient and pot-economic approach in a single vessel has been developed for conversion of aromatic and aliphatic carboxamides into primary amines with one fewer carbom atom (Hofmann reaction) in 38–89 % yield by reacting with trichloro- or tribromoisocyanuric acid and sodium hydroxide in aqueous acetonitrile. Under the same reaction conditions, cyclic imides gave amino acids (69–83 %). The role of the trihaloisocyanuric acids is the in situ generation of N-haloamides, key-intermediates for the Hofmann reaction. The scalability of the methodology was demonstrated by a multigram-scale transformation of phthalimide into anthranilic acid in 77 % yield.

Method for preparing primary amine by catalyzing reductive amination of aldehyde ketone compounds

-

Paragraph 0027-0030; 0051-0055, (2020/05/30)

The invention discloses a method for preparing primary amine by catalyzing reductive amination of aldehyde ketone compounds. The method comprises the following steps: 1) mixing nickel nitrate hexahydrate, citric acid and an organic solvent, carrying out heating and stirring until a colloidal material is obtained, drying the colloidal material, roasting the colloidal material in a protective atmosphere, pickling, washing and drying a roasted product, and performing a partial oxidation reaction on a dried product in an oxygen-nitrogen mixed atmosphere to obtain a catalyst for a reductive amination reaction; and 2) mixing aldehyde or ketone compounds, a methanol solution of ammonia and the reductive amination reaction catalyst, introducing hydrogen, and carrying out a reductive amination reaction. The method has the advantages of high primary amine yield, high selectivity, wide aldehyde ketone substrate range, short reaction time, mild reaction conditions, low cost, greenness, economicalperformance and the like; the used reductive amination reaction catalyst can be recycled more than 10 times, and the catalytic activity of the catalyst is not obviously changed in gram-level reactions; and the method is suitable for large-scale application.

Photochemical Decarboxylative C(sp3)-X Coupling Facilitated by Weak Interaction of N-Heterocyclic Carbene

Chen, Kun-Quan,Wang, Zhi-Xiang,Chen, Xiang-Yu

supporting information, p. 8059 - 8064 (2020/11/02)

While N-hydroxyphthalimide (NHPI) ester has emerged as a powerful reagent as an alkyl radical source for a variety of C-C bond formations, the corresponding C(sp3)-N bond formation is still in its infancy. We demonstrate herein transition-metal-free decarboxylative C(sp3)-X bond formation enabled by the photochemical activity of the NHPI ester-NaI-NHC complex, giving primary C(sp3)-(N)phth, secondary C(sp3)-I, or tertiary C(sp3)-(meta C)phth coupling products. The primary C(sp3)-(N)phth coupling offers convenient access to primary amines.

A State-of-the-Art Heterogeneous Catalyst for Efficient and General Nitrile Hydrogenation

Formenti, Dario,Mocci, Rita,Atia, Hanan,Dastgir, Sarim,Anwar, Muhammad,Bachmann, Stephan,Scalone, Michelangelo,Junge, Kathrin,Beller, Matthias

supporting information, p. 15589 - 15595 (2020/10/02)

Cobalt-doped hybrid materials consisting of metal oxides and carbon derived from chitin were prepared, characterized and tested for industrially relevant nitrile hydrogenations. The optimal catalyst supported onto MgO showed, after pyrolysis at 700 °C, magnesium oxide nanocubes decorated with carbon-enveloped Co nanoparticles. This special structure allows for the selective hydrogenation of diverse and demanding nitriles to the corresponding primary amines under mild conditions (e.g. 70 °C, 20 bar H2). The advantage of this novel catalytic material is showcased for industrially important substrates, including adipodinitrile, picolinonitrile, and fatty acid nitriles. Notably, the developed system outperformed all other tested commercial catalysts, for example, Raney Nickel and even noble-metal-based systems in these transformations.

Facile synthesis of controllable graphene-co-shelled reusable Ni/NiO nanoparticles and their application in the synthesis of amines under mild conditions

Cui, Zhibing,Liu, Jianguo,Liu, Qiying,Ma, Longlong,Singh, Thishana,Wang, Chenguang,Wang, Nan,Zhu, Yuting

supporting information, p. 7387 - 7397 (2020/11/19)

The primary objective of many researchers in chemical synthesis is the development of recyclable and easily accessible catalysts. These catalysts should preferably be made from Earth-abundant metals and have the ability to be utilised in the synthesis of pharmaceutically important compounds. Amines are classified as privileged compounds, and are used extensively in the fine and bulk chemical industries, as well as in pharmaceutical and materials research. In many laboratories and in industry, transition metal catalysed reductive amination of carbonyl compounds is performed using predominantly ammonia and H2. However, these reactions usually require precious metal-based catalysts or RANEY nickel, and require harsh reaction conditions and yield low selectivity for the desired products. Herein, we describe a simple and environmentally friendly method for the preparation of thin graphene spheres that encapsulate uniform Ni/NiO nanoalloy catalysts (Ni/NiO?C) using nickel citrate as the precursor. The resulting catalysts are stable and reusable and were successfully used for the synthesis of primary, secondary, tertiary, and N-methylamines (more than 62 examples). The reaction couples easily accessible carbonyl compounds (aldehydes and ketones) with ammonia, amines, and H2 under very mild industrially viable and scalable conditions (80 °C and 1 MPa H2 pressure, 4 h), offering cost-effective access to numerous functionalized, structurally diverse linear and branched benzylic, heterocyclic, and aliphatic amines including drugs and steroid derivatives. We have also demonstrated the scale-up of the heterogeneous amination protocol to gram-scale synthesis. Furthermore, the catalyst can be immobilized on a magnetic stirring bar and be conveniently recycled up to five times without any significant loss of catalytic activity and selectivity for the product.

Deacetylative Amination of Acetyl Arenes and Alkanes with C-C Bond Cleavage

Hyodo, Kengo,Hasegawa, Genna,Maki, Hiroya,Uchida, Kingo

supporting information, p. 2818 - 2822 (2019/04/25)

The Br?nsted acid-catalyzed synthesis of primary amines from acetyl arenes and alkanes with C-C bond cleavage is described. Although the conversion from an acetyl group to amine has traditionally required multiple steps, the method described herein, which uses an oxime reagent as an amino group source, achieves the transformation directly via domino transoximation/Beckmann rearrangement/Pinner reaction. The method was also applied to the synthesis of γ-aminobutyric acids, such as baclophen and rolipram.

PRODUCTION METHOD OF PRIMARY AMINE COMPOUND

-

Paragraph 0029, (2019/09/20)

PROBLEM TO BE SOLVED: To provide a simple production method of a primary amine compound unnecessary for complicated procedures and toxic sodium azide or the like. SOLUTION: A production method of a primary amine compound includes a step for reacting a ketone compound and an oxime compound in the presence of alcohol and an acid catalyst. Preferably, the acid catalyst is hydrochloric acid, sulfuric acid, methanesulfonic acid, camphorsulfonic acid, a tosyl acid hydrate, trifluoromethane sulfonic acid or a boron trifluoride diethyl ether complex. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

A Mild and Base-Free Protocol for the Ruthenium-Catalyzed Hydrogenation of Aliphatic and Aromatic Nitriles with Tridentate Phosphine Ligands

Adam, Rosa,Bheeter, Charles Beromeo,Jackstell, Ralf,Beller, Matthias

, p. 1329 - 1334 (2016/04/20)

A novel protocol for the general hydrogenation of nitriles in the absence of basic additives is described. The system is based on the combination of [Ru(cod)(methylallyl)2] (cod=cyclooctadiene) and L2. A variety of aromatic and aliphatic nitriles is hydrogenated under mild conditions (50 °C and 15 bar H2) with this system. Kinetic studies revealed higher activity in the case of aromatic nitriles compared with aliphatic ones.

Integrated Heterogeneous Metal/Enzymatic Multiple Relay Catalysis for Eco-Friendly and Asymmetric Synthesis

Palo-Nieto, Carlos,Afewerki, Samson,Anderson, Mattias,Tai, Cheuk-Wai,Berglund, Per,Córdova, Armando

, p. 3932 - 3940 (2016/07/06)

Organic synthesis is in general performed using stepwise transformations where isolation and purification of key intermediates is often required prior to further reactions. Herein we disclose the concept of integrated heterogeneous metal/enzymatic multiple relay catalysis for eco-friendly and asymmetric synthesis of valuable molecules (e.g., amines and amides) in one-pot using a combination of heterogeneous metal and enzyme catalysts. Here reagents, catalysts, and different conditions can be introduced throughout the one-pot procedure involving multistep catalytic tandem operations. Several novel cocatalytic relay sequences (reductive amination/amidation, aerobic oxidation/reductive amination/amidation, reductive amination/kinetic resolution and reductive amination/dynamic kinetic resolution) were developed. They were next applied to the direct synthesis of various biologically and optically active amines or amides in one-pot from simple aldehydes, ketones, or alcohols, respectively.

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