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17373-29-4

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17373-29-4 Usage

General Description

N,N-Dimethyltridecylamine is a tertiary amine. Its 7-oxabicyclo[2.2.l]heptane- 2,3-dicarboxylic acid salt (endothall) in combination with pyrazon has been used as major herbicide to control annual weeds in sugar beets.

Check Digit Verification of cas no

The CAS Registry Mumber 17373-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17373-29:
(7*1)+(6*7)+(5*3)+(4*7)+(3*3)+(2*2)+(1*9)=114
114 % 10 = 4
So 17373-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H33N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16(2)3/h4-15H2,1-3H3

17373-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyltridecan-1-amine

1.2 Other means of identification

Product number -
Other names 1-(Dimethylamino)tridecane

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:17373-29-4 SDS

17373-29-4Downstream Products

17373-29-4Relevant articles and documents

N-Methylation of amines and nitroarenes with methanol using heterogeneous platinum catalysts

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

, p. 47 - 56 (2019/02/07)

We report herein the selective N-methylation of amines and nitroarenes with methanol under basic conditions using carbon-supported Pt nanoparticles (Pt/C) as a heterogeneous catalyst. This method is widely applicable to four types of N-methylation reactions: (1) N,N-dimethylation of aliphatic amines under N2, (2) N-monomethylation of aliphatic amines under 40 bar H2, (3) N-monomethylation of aromatic amines under N2, and (4) tandem synthesis of N-methyl anilines from nitroarenes and methanol under 2 bar H2. All these reactions under the same catalytic system showed high yields of the corresponding methylamines for a wide range of substrates, high turnover number (TON), and good catalyst reusability. Mechanistic studies suggested that the reaction proceeded via a borrowing hydrogen methodology. Kinetic results combined with density functional theory (DFT) calculations revealed that the high performance of Pt/C was ascribed to the moderate metal–hydrogen bond strength of Pt.

PROCESS FOR MAKING LONG CHAIN INTERNAL FATTY TERTIARY AMINES

-

Page/Page column 17; 18, (2010/11/30)

The invention relates to a process for preparing long chain internal fatty amines, quaternized amines and amine oxides and selected amine oxides having a symmetric alkyl portion.

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