1838-19-3

Basic information

• Product Name: oleylamine
• Synonyms: SKF-38094;NSC 66461
• CAS NO: 1838-19-3
• Molecular Formula: C₁₈H₃₇N
• Molecular Weight: 267.49
• EINECS: 204-015-5;223-293-9
• Mol File: 1838-19-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 15-22℃
• Boiling Point: 364.4°Cat760mmHg
• Flash Point: 154.4°C
• Appearance: /
• Density: 0.828g/cm³
• Vapor Pressure: 1.69E-05mmHg at 25°C
• Refractive Index: 1.463
• Water Solubility: insoluble
• CAS DataBase Reference: oleylamine(CAS DataBase Reference)
• NIST Chemistry Reference: oleylamine(1838-19-3)
• EPA Substance Registry System: oleylamine(1838-19-3)

Safety Data

• Hazard Codes: C:Corrosive
• Statements: R22:; R34:
• Safety Statements: S24/25:; S26:
• Hazardous Substances Data: 1838-19-3(Hazardous Substances Data)

Usage

General Description

Oleylamine is a chemical compound classified as an amine, which is a derivative of ammonia with one or more hydrogen atoms replaced by organic groups. It is commonly used as a surfactant and stabilizer in various applications such as in the synthesis of nanoparticles, as a solvent for organic compounds, and as an intermediate in the manufacturing of various chemical products. Oleylamine is a liquid at room temperature, with a characteristic amine odor, and is soluble in organic solvents. It is typically produced from natural sources such as animal and vegetable fats, and is considered to be a versatile and important chemical in the field of organic chemistry and industrial applications.

InChI:InChI=1/C18H37N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h9-10H,2-8,11-19H2,1H3/b10-9-

Upstream product

• 4303-70-2 (E)-9-octadecenoic acid amide 
• 19491-41-9 elaidonitrile 
• 112-77-6 elaidoyl chloride 
• 112-79-8 Elaidic acid 
• 112-90-3 (Z)-9-octadecen-1-amine 
• 921620-98-6 elaidylamine hydrochloride 

Downstream Products

• 82448-16-6 (Z)-N-(octadec-9-en-1-yl)acetamide 
• 1338440-05-3 C₂₆H₄₄N₂S 
• 25307-17-9 2,2'-(octadec-9-en-1-ylimino)diethanol 

Relevant articles and documents

Photoinduced remote regioselective radical alkynylation of unactivated C-H bonds

A method for the remote regioselective alkynylation of unactivated C(sp3)-H bonds in diverse aliphatic amides by photogenerated amidyl radicals has been developed. The site-selectivity is dominated via a 1,5-hydrogen atom transfer (HAT) process of the amide. Mild reaction conditions and high regioselectivity are demonstrated in this methodology.

Process for the preparation of saturated or unsaturated primary fatty amines

Process for the preparation of unsaturated and saturated primary fatty amines comprising the steps of chlorination, treatment by ammonia, reduction and purification

Nematicidal activity of N-substituted and N,N-disubstituted alkylamines against the pine wood nematode, Bursaphelenchus xylophilus

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