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Benzenepropanol, α-tridecyl-, also known as 3-phenyl-1-tridecanol or 3-phenylpropyl tallow alcohol, is a synthetic organic compound with the chemical formula C19H36O. It is a derivative of benzenepropanol, where a tallow alkyl chain (a mixture of triglycerides derived from tallow, a rendered form of animal fat) is attached to the α-carbon atom. Benzenepropanol, a-tridecyl- is primarily used as a nonionic surfactant in various industrial applications, such as detergents, emulsifiers, and foaming agents. Due to its amphiphilic nature, it can lower the surface tension of water and help mix oil and water, making it a valuable component in the formulation of personal care products, textiles, and other consumer goods.

176791-06-3

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176791-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176791-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,7,9 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 176791-06:
(8*1)+(7*7)+(6*6)+(5*7)+(4*9)+(3*1)+(2*0)+(1*6)=173
173 % 10 = 3
So 176791-06-3 is a valid CAS Registry Number.

176791-06-3SDS

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 1-phenylhexadecan-3-ol

1.2 Other means of identification

Product number -
Other names -

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:176791-06-3 SDS

176791-06-3Downstream Products

176791-06-3Relevant academic research and scientific papers

A reaction for sp3-sp3 C-C bond formation via cooperation of Lewis acid-promoted/Rh-catalyzed C-H bond activation

Shi, Lei,Tu, Yong-Qiang,Wang, Min,Zhang, Fu-Min,Fan, Chun-An,Zhao, Yu-Ming,Xia, Wu-Jiong

, p. 10836 - 10837 (2007/10/03)

A new method for intermolecular sp3-sp3 C-C bond formation between primary aliphatic alcohol and olefin by use of a RhCl(PPh3)3 (cat.)/BF3·OEt2 (2.5 equiv)/BuBr (0.5 equiv)/toluene system was first disclosed, which possessed quite significant utilities for organic synthesis, especially for that of secondary alcohols. The most significant aspect is the discovery that rhodium-catalyzed C-H bond activation of alcohols is feasible under Lewis acid-promoted conditions. Copyright

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