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N,N-dimethylpentadecylamine is an organic chemical compound that belongs to the amine class. It features a pentadecyl chain, a long hydrocarbon chain with 15 carbon atoms, and is characterized by the presence of two methyl groups attached to a nitrogen atom. N,N-dimethylpentadecylamine is recognized for its capacity to reduce the surface tension of liquids, thereby promoting the mixing of substances that are usually immiscible.

17678-60-3

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17678-60-3 Usage

Uses

Used in Personal Care Products:
N,N-dimethylpentadecylamine is utilized as a surfactant and emulsifier in the production of personal care products, enhancing the stability and texture of formulations, and ensuring the even distribution of ingredients.
Used in Pharmaceuticals:
In the pharmaceutical industry, N,N-dimethylpentadecylamine serves as a surfactant and emulsifier, playing a crucial role in the formulation of medications, improving the solubility and absorption of active pharmaceutical ingredients.
Used in Lubricants:
N,N-dimethylpentadecylamine is employed as an additive in lubricants to improve their performance, reducing friction and wear, and providing better protection for moving parts in various mechanical applications.
Used in Chemical Synthesis:
N,N-dimethylpentadecylamine is also used as an intermediate in the synthesis of other chemical compounds, contributing to the creation of a wide range of products across different industries.
Used as a Corrosion Inhibitor:
N,N-dimethylpentadecylamine functions as a corrosion inhibitor, protecting materials from the damaging effects of corrosion, extending their service life, and ensuring the integrity of structures and equipment.
It is important to handle N,N-dimethylpentadecylamine with care due to its potential harmful effects if inhaled, ingested, or if it comes into contact with the skin or eyes. Proper safety measures should be taken during its use to minimize any risks associated with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 17678-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17678-60:
(7*1)+(6*7)+(5*6)+(4*7)+(3*8)+(2*6)+(1*0)=143
143 % 10 = 3
So 17678-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H37N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2)3/h4-17H2,1-3H3

17678-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethylpentadecan-1-amine

1.2 Other means of identification

Product number -
Other names dimethyl-pentadecyl-amine

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:17678-60-3 SDS

17678-60-3Downstream Products

17678-60-3Relevant academic research and scientific papers

Methylformate as replacement of syngas in one-pot catalytic synthesis of amines from olefins

Karakhanov, Eduard,Maksimov, Anton,Kardasheva, Yulia,Runova, Elena,Zakharov, Roman,Terenina, Maria,Kenneally, Corey,Arredondo, Victor

, p. 540 - 547 (2014/02/14)

A new general approach for the one-pot hydroaminomethylation of olefins using methylformate as formylating agent instead of synthesis gas (syngas) has been proposed. Herein we report that a Ru-Rh catalytic system demonstrates high activity in a tandem conversion of a series of n-alkenes into amines using methylformate with yields 58-92% (6 h). The selectivity for the normal amine reached 96% with catalysis by the Ru carbonyl complex Ru3(CO) 12, with an overall yield of 55% with respect to amine in this instance. The addition of the Rh complex to Ru catalytic system, sharply increased the hydroaminomethylation rate of both the terminal and internal alkenes and increased the yield of amines to 82-93% (6-12 h). The Royal Society of Chemistry.

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