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629-79-8

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629-79-8 Usage

Description

Hexadecanenitrile, with the molecular formula C16H33N, is a nitrile compound characterized by a carbon-nitrogen triple bond. It is a colorless to pale yellow liquid with a faint odor, insoluble in water, and soluble in organic solvents. This chemical compound serves as a versatile raw material in various industries due to its unique properties.

Uses

Used in Pharmaceutical Industry:
Hexadecanenitrile is used as a raw material for the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds due to its reactive carbon-nitrogen triple bond.
Used in Dye and Perfume Industry:
In the dye and perfume industry, hexadecanenitrile is utilized as a starting material for the synthesis of dyes and fragrances, leveraging its chemical reactivity to create a range of colorants and aromatic compounds.
Used in Plastics and Rubber Industry:
Hexadecanenitrile is employed in the manufacturing of plastics and rubber, where it serves as a key component in the production of various types of polymers, enhancing their properties and performance.
Used in Adhesives Industry:
In the adhesives industry, hexadecanenitrile is used as a component in the formulation of adhesives, contributing to the development of strong and durable bonding agents.
Used in Chemical Research and Analysis:
Hexadecanenitrile is utilized as a reagent and intermediate in organic synthesis within the field of chemical research and analysis, facilitating various chemical reactions and the synthesis of complex organic compounds.
Safety Note:
Due to its potential toxicity and irritating properties, hexadecanenitrile should be handled with caution, employing proper safety measures to minimize risks during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 629-79-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 629-79:
(5*6)+(4*2)+(3*9)+(2*7)+(1*9)=88
88 % 10 = 8
So 629-79-8 is a valid CAS Registry Number.
InChI:InChI=1S/C16H31N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-15H2,1H3

629-79-8SDS

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 hexadecanenitrile

1.2 Other means of identification

Product number -
Other names 1-Cyanopentadecane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:629-79-8 SDS

629-79-8Relevant articles and documents

Dehydrogenation of Primary Alkyl Azides to Nitriles Catalyzed by Pincer Iridium/Ruthenium Complexes

Gan, Lan,Jia, Xiangqing,Fang, Huaquan,Liu, Guixia,Huang, Zheng

, p. 3661 - 3665 (2020/06/02)

Pincer metal complexes exhibit superior catalytic activity in the dehydrogenation of plain alkanes, but find limited application in the dehydrogenation of functionalized organic molecules. Starting from easily accessible primary alkyl azides, here we report an efficient dehydrogenation of azides to nitriles using pincer iridium or ruthenium complexes as the catalysts. This method offers a route to cyanide-free preparation of nitriles without carbon chain elongation and without the use of strong oxidants. Both benzyl and linear aliphatic azides can be dehydrogenated with tert-butylethylene as the hydrogen acceptor to afford nitriles in moderate to high yields. Various functional groups can be tolerated, and the H?C?C?H bond dehydrogenation does not occur for linear alkyl azide substrates. Furthermore, the pincer Ir catalytic system was found to catalyze the direct azide dehydrogenation without the use of a sacrificial hydrogen acceptor.

Selective Transformations of Triglycerides into Fatty Amines, Amides, and Nitriles by using Heterogeneous Catalysis

Jamil, Md. A. R.,Siddiki, S. M. A. Hakim,Touchy, Abeda Sultana,Rashed, Md. Nurnobi,Poly, Sharmin Sultana,Jing, Yuan,Ting, Kah Wei,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-ichi

, p. 3115 - 3125 (2019/04/26)

The use of triglycerides as an important class of biomass is an effective strategy to realize a more sustainable society. Herein, three heterogeneous catalytic methods are reported for the selective one-pot transformation of triglycerides into value-added chemicals: i) the reductive amination of triglycerides into fatty amines with aqueous NH3 under H2 promoted by ZrO2-supported Pt clusters; ii) the amidation of triglycerides under gaseous NH3 catalyzed by high-silica H-beta (Hβ) zeolite at 180 °C; iii) the Hβ-promoted synthesis of nitriles from triglycerides and gaseous NH3 at 220 °C. These methods are widely applicable to the transformation of various triglycerides (C4–C18 skeletons) into the corresponding amines, amides, and nitriles.

Merging visible-light photoredox and copper catalysis in catalytic aerobic oxidation of amines to nitriles

Tao, Chuanzhou,Wang, Bin,Sun, Lei,Liu, Zhou,Zhai, Yadong,Zhang, Xiulian,Wang, Jian

supporting information, p. 328 - 332 (2017/01/13)

Visible-light-initiated homogeneous oxidative synthesis of nitriles from amines was accomplished through a combined use of photoredox and copper catalysis. This transformation was performed at room temperature with O2 as the oxidant.

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