N31001
Nonylamine
98%
Synonym(s):
1-Aminononane
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About This Item
Linear Formula:
CH3(CH2)8NH2
CAS Number:
Molecular Weight:
143.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-945-9
Beilstein/REAXYS Number:
1733633
MDL number:
Assay:
98%
Form:
liquid
Product Name
Nonylamine, 98%
InChI
1S/C9H21N/c1-2-3-4-5-6-7-8-9-10/h2-10H2,1H3
SMILES string
CCCCCCCCCN
InChI key
FJDUDHYHRVPMJZ-UHFFFAOYSA-N
assay
98%
form
liquid
refractive index
n20/D 1.433 (lit.)
bp
201 °C (lit.)
density
0.782 g/mL at 25 °C (lit.)
Quality Level
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Application
- 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).
General description
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.
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Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
165.2 °F - closed cup
flash_point_c
74 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Structural chemistry and properties of metal arenesulfonates
Cai, Jiwen, et al.
Coordination Chemistry Reviews, 248, 1061-1083 (2004)
Crystal structure of amine oxidase from bovine serum
Lunelli, Michele and Di Paolo, Maria Luisa and Biadene,. et al.
Journal of Molecular Biology, 346, 991-1004 (2005)
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)
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