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Oleylamine hydrochloride is the hydrochloride salt of oleylamine, a long-chain unsaturated fatty amine. It is a water-soluble compound known for its unique properties, making it an important chemical in various fields such as materials science, nanotechnology, and the production of specialty chemicals and pharmaceutical formulations.

41130-29-4

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41130-29-4 Usage

Uses

Used in Coatings Industry:
Oleylamine hydrochloride is used as a surfactant and emulsifier for improving the stability and performance of coatings. Its ability to reduce surface tension and form stable emulsions enhances the dispersion of pigments and other additives, leading to improved coating properties.
Used in Lubricants Industry:
Oleylamine hydrochloride serves as a corrosion inhibitor in lubricants, protecting metal surfaces from wear and corrosion. Its adsorption on metal surfaces forms a protective film, reducing friction and extending the life of machinery and equipment.
Used in Pharmaceutical Industry:
Oleylamine hydrochloride is used as a stabilizing agent for metal nanoparticles in drug delivery systems. Its interaction with metal ions provides stability and controlled release of therapeutic agents, improving the efficacy and safety of pharmaceutical formulations.
Used in Materials Science and Nanotechnology:
Oleylamine hydrochloride acts as a precursor for the synthesis of other amine compounds and serves as a stabilizing agent for the formation of metal nanoparticles. Its ability to control the size, shape, and dispersion of nanoparticles contributes to the development of advanced materials with unique properties and applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 41130-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,3 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41130-29:
(7*4)+(6*1)+(5*1)+(4*3)+(3*0)+(2*2)+(1*9)=64
64 % 10 = 4
So 41130-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H35NO.ClH/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;/h9-10H,2-8,11-17H2,1H3,(H2,19,20);1H/b10-9-;

41130-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-octadec-9-en-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names Oleylamine HCl

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:41130-29-4 SDS

41130-29-4Upstream product

41130-29-4Downstream Products

41130-29-4Relevant academic research and scientific papers

Chemically Tailoring the Dopant Emission in Manganese-Doped CsPbCl3 Perovskite Nanocrystals

Das Adhikari, Samrat,Dutta, Sumit K.,Dutta, Anirban,Guria, Amit K.,Pradhan, Narayan

, p. 8746 - 8750 (2017)

Doping in perovskite nanocrystals adopts different mechanistic approach in comparison to widely established doping in chalcogenide quantum dots. The fast formation of perovskites makes the dopant insertions more competitive and challenging. Introducing alkylamine hydrochloride (RNH3Cl) as a promoting reagent, precise controlled doping of MnII in CsPbCl3 perovskite nanocrystals is reported. Simply, by changing the amount of RNH3Cl, the Mn incorporation and subsequent tuning in the excitonic as well as Mn d–d emission intensities are tailored. Investigations suggested that RNH3Cl acted as the chlorinating source, controlled the size, and also helps in increasing the number of particles. This provided more opportunity for Mn ions to take part in reaction and occupied the appropriate lattice positions. Carrying out several reactions with varying reaction parameters, the doping conditions are optimized and the role of the promoting reagent for both doped and undoped systems are compared.

Process for the preparation of saturated or unsaturated primary fatty amines

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Page/Page column 4-5, (2008/06/13)

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

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