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Documentos Principais

N31001

Sigma-Aldrich

Nonylamine

98%

Sinônimo(s):

1-Aminononane

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About This Item

Fórmula linear:
CH3(CH2)8NH2
Número CAS:
Peso molecular:
143.27
Beilstein:
1733633
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

98%

Formulário

liquid

índice de refração

n20/D 1.433 (lit.)

p.e.

201 °C (lit.)

densidade

0.782 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCN

InChI

1S/C9H21N/c1-2-3-4-5-6-7-8-9-10/h2-10H2,1H3

chave InChI

FJDUDHYHRVPMJZ-UHFFFAOYSA-N

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Descrição geral

Nonylamineis a versatile organic compound belongs to the class of primary amines. It hashydrophobic properties because of its long hydrocarbon chain. Nonylamine isoften used as building block in various chemical reactions,including alkylation and acylation processes. In coordination chemistry,nonylamine acts as a ligand, forming complexes with metals that can be used incatalysis and material science applications. Its long hydrocarbon chain allowsfor increased solubility in organic solvents, facilitating reactions thatrequire hydrophobic environments.

Aplicação


  • Contribution of liquid-phase and gas-phase ionization in extractive electrospray ionization mass spectrometry of primary amines.: This study discusses the dual ionization mechanisms in mass spectrometry, which could be crucial for analyzing chemical reactions involving nonylamine in both phases, providing a detailed methodology for chemists focused on reaction mechanisms and molecular analysis (Meier et al., 2011).

  • Solvent-free derivatization of pristine multi-walled carbon nanotubes with amines.: This research provides insights into the solvent-free functionalization of carbon nanotubes with amines, including potentially nonylamine, which is significant for chemical engineers working on advanced material coatings and functionalities (Basiuk et al., 2005).

  • Enhanced in vitro percutaneous penetration of salicylate by ion pair formation with alkylamines.: This article explores how alkylamines, possibly including nonylamine, enhance the penetration of salicylate through the skin, which is valuable for pharmaceutical scientists developing topical treatments (Kadono et al., 1998).

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

165.2 °F - closed cup

Ponto de fulgor (°C)

74 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Octadecylamine technical grade, 90%

Sigma-Aldrich

O1408

Octadecylamine

Detection of Hb-Papio B, a silent mutation of the baboon beta chain, by high performance liquid chromatography. Improved procedures for the separation of globin chains by HPLC.
J B Shelton et al.
Hemoglobin, 6(5), 451-464 (1982-01-01)
Daniel Merino-García et al.
Archives of environmental contamination and toxicology, 45(3), 289-296 (2003-12-17)
The toxicity of two amines, nonylamine and decylamine, which have a narcotic effect on organisms, and ethylparathion (enzymatic inhibitor) on Daphnia magna has been studied when acting singly and in joint toxicity tests. This was done on the basis of
Anzi Wang et al.
Journal of chromatography. A, 1374, 216-223 (2014-12-06)
Fabrication technologies for microelectromechanical systems (MEMS) allow miniaturization of conventional benchtop gas chromatography (GC) to portable, palm-sized microfabricated GC (μGC) devices, which are suitable for on-site chemical analysis and remote sensing. The separation performance of μGC systems, however, has not

Protocolos

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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