- Decylamine
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- $8.00 / 1KG
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2025-09-25
- CAS:2016-57-1
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
- Decylamine
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- $30.00 / 1KG
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2025-06-27
- CAS:2016-57-1
- Min. Order: 50KG
- Purity: 99%
- Supply Ability: 500000kg
- Decylamine
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- $50.00 / 1kg
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2025-06-20
- CAS:2016-57-1
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 10 tons
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| | Decylamine Basic information |
| | Decylamine Chemical Properties |
| Melting point | 12-14 °C(lit.) | | Boiling point | 216-218 °C(lit.) | | density | 0.787 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.436(lit.) | | Fp | 186 °F | | storage temp. | room temp | | solubility | Chloroform, Ethyl Acetate | | pka | 10.64(at 25℃) | | form | Liquid | | color | Clear colorless to yellow or brown | | BRN | 1735220 | | Stability: | Stable. Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides. Absorbs carbon dioxide from the air. | | CAS DataBase Reference | 2016-57-1(CAS DataBase Reference) | | NIST Chemistry Reference | 1-Decanamine(2016-57-1) | | EPA Substance Registry System | Decylamine (2016-57-1) |
| | Decylamine Usage And Synthesis |
| Chemical Properties | It is a clear, colorless, flammable, liquid with a ammonia odor. Slightly soluble in water, easily soluble in ethanol, ether, acetone, benzene and chloroform. | | Uses | 1-Decylamine is a intermediate forming the phosphatidylcholine-decylamine liposomal membranes. | | Uses | Decylamine was used in the synthesis of dynole 2-24 series by undergoing reductive amination with 1-(3-(dimethylamino)propyl)-1H-indole-3-carbaldehyde. It was also used as a coordinating solvent to thermolyse the lead piperidine and lead tetrahydroquinoline dithiocarbamate (DTC) complexes. | | Application | Decylamine has been used as:
Amine in the synthesis of dynole-2-24 by reductive amination with 1-(3-(dimethylamino)propyl)-1H-indole-3-carbaldehyde.
A modifier in the synthesis of nanocomposites based on poly(butylene terephthalate) and C60 nanoparticles.
A template in the synthesis of ordered two and three dimensional mesoporous iron oxide. | | Definition | ChEBI: Decylamine is an alkylamine. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 43, p. 2259, 1978 DOI: 10.1021/jo00405a036
Synthesis, p. 450, 1989 DOI: 10.1055/s-1989-27284 | | General Description | Decylamine is a hydrophobic long alkylated cationic ammonium that is used to modify the polarity of reversed phases on octadecylsilyl (ODS) gels. | | Safety Profile | Poison by ingestion and
skin contact. A skin irritant. Flammable
when exposed to heat or flame; can react
with oxidizing materials. To fight fue, use
alcohol foam, foam, dry chemical. When
heated to decomposition it emits toxic
fumes of NOx. See AMINES and AMINES,
FATTY. | | Properties and Applications | Decylamine (C10H21NH2) is a primary alkylamine with a long hydrophobic tail. Decylamine molecules were directly intercalated as guest molecules into a layered silicate, octosilicate, with hydrogen ions in the interlayers (H-octosilicate) as a host material by using a wet process with various solvents of different polarities and decylamine solubilities. Using a solvent with a relatively high polarity promoted the intercalation of decylamine molecules. In particular, when water, a poor solvent for decylamine, was used, the decylamine molecules were well-ordered in the interlayer space of H-octosilicate. The interlayer distance corresponded to double the length of the decylamine molecule, suggesting the formation of a decylamine bilayer in the interlayer space. The study suggests that the solvation of decylamine molecules can determine the structure of intercalated octosilicate compounds. n-decylamine is a good inhibitor of zinc in hydrochloric acid solution. Halide ions enhanced the corrosion of zinc, whereas n-decylamine inhibited the corrosion of zinc. The inhibitor efficiency of n-decylamine is increased significantly by halide ions. A consistent surface coverage value is obtained from weight loss and polarization studies, and n-decylamine acts mainly as a cathodic inhibitor[1-2].
| | References |
[1] Iwasaki, Tomohiro. “Effect of solvents on the direct intercalation of decylamine into H-octosilicate.” Applied Clay Science 199 (2020): Article 105882.
[2] H.B. Rudresh, S.M. Mayanna. “The synergistic effect of Halide ions on the corrosion inhibition of zinc by n-decylamine.” Corrosion Science 19 6 (1979): Pages 361-370.
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| | Decylamine Preparation Products And Raw materials |
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