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16165-33-6

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16165-33-6 Usage

Uses

Diundecylamine is used as a reactant in the synthesis of symmetrical two-tailed dendritic tricarboxylato amphiphiles.

Check Digit Verification of cas no

The CAS Registry Mumber 16165-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16165-33:
(7*1)+(6*6)+(5*1)+(4*6)+(3*5)+(2*3)+(1*3)=96
96 % 10 = 6
So 16165-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H47N/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h23H,3-22H2,1-2H3

16165-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-undecylundecan-1-amine

1.2 Other means of identification

Product number -
Other names di-n-Undecylamine

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:16165-33-6 SDS

16165-33-6Relevant articles and documents

One-pot reductive amination of carboxylic acids: a sustainable method for primary amine synthesis

Coeck, Robin,De Vos, Dirk E.

supporting information, p. 5105 - 5114 (2020/08/25)

The reductive amination of carboxylic acids is a very green, efficient and sustainable method for the production of (bio-based) amines. However, with current technology, this reaction requires two to three reaction steps. Here, we report the first (heterogeneous) catalytic system for the one-pot reductive amination of carboxylic acids to amines, with solely H2 and NH3 as the reactants. This reaction can be performed with relatively cheap ruthenium-tungsten bimetallic catalysts in the green and benign solvent cyclopentyl methyl ether (CPME). Selectivities of up to 99% for the primary amine could be achieved at high conversions. Additionally, the catalyst is recyclable and tolerant for common impurities such as water and cations (e.g. sodium carboxylate).

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